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Published in: Cancer and Metastasis Reviews 1-2/2013

01-06-2013 | NON-THEMATIC REVIEW

Reversal of ATP-binding cassette drug transporter activity to modulate chemoresistance: why has it failed to provide clinical benefit?

Authors: Man Yu, Alberto Ocana, Ian F. Tannock

Published in: Cancer and Metastasis Reviews | Issue 1-2/2013

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Abstract

Enhanced drug extrusion from cells due to the overexpression of the ATP-binding cassette (ABC) drug transporters inhibits the cytotoxic effects of structurally diverse and mechanistically unrelated anticancer agents and is a major cause of multidrug resistance (MDR) of human malignancies. Multiple compounds can suppress the activity of these efflux transporters and sensitize resistant tumor cells, but despite promising preclinical and early clinical data, they have yet to find a role in oncologic practice. Based on the knowledge of the structure, function, and distribution of MDR-related ABC transporters and the results of their preclinical and clinical evaluation, we discuss probable reasons why these inhibitors have not improved the outcome of therapy for cancer patients. We also outline new MDR-reversing strategies that directly target ABC transporters or circumvent relevant signaling pathways.
Literature
1.
go back to reference Gillet, J. P., & Gottesman, M. M. (2011). Advances in the molecular detection of ABC transporters involved in multidrug resistance in cancer. Current Pharmaceutical Biotechnology, 12, 686–692.PubMedCrossRef Gillet, J. P., & Gottesman, M. M. (2011). Advances in the molecular detection of ABC transporters involved in multidrug resistance in cancer. Current Pharmaceutical Biotechnology, 12, 686–692.PubMedCrossRef
2.
go back to reference Ueda, K. (2011). ABC proteins protect the human body and maintain optimal health. Bioscience, Biotechnology, and Biochemistry, 75, 401–409.PubMedCrossRef Ueda, K. (2011). ABC proteins protect the human body and maintain optimal health. Bioscience, Biotechnology, and Biochemistry, 75, 401–409.PubMedCrossRef
3.
go back to reference Juliano, R. L., & Ling, V. (1976). A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochimica et Biophysica Acta, 455, 152–162.PubMedCrossRef Juliano, R. L., & Ling, V. (1976). A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochimica et Biophysica Acta, 455, 152–162.PubMedCrossRef
4.
go back to reference Zhou, S. F. (2008). Structure, function and regulation of P-glycoprotein and its clinical relevance in drug disposition. Xenobiotica, 38, 802–832.PubMedCrossRef Zhou, S. F. (2008). Structure, function and regulation of P-glycoprotein and its clinical relevance in drug disposition. Xenobiotica, 38, 802–832.PubMedCrossRef
5.
go back to reference Loo, T. W., Bartlett, M. C., & Clarke, D. M. (2003). Drug binding in human P-glycoprotein causes conformational changes in both nucleotide-binding domains. Journal of Biological Chemistry, 278, 1575–1578.PubMedCrossRef Loo, T. W., Bartlett, M. C., & Clarke, D. M. (2003). Drug binding in human P-glycoprotein causes conformational changes in both nucleotide-binding domains. Journal of Biological Chemistry, 278, 1575–1578.PubMedCrossRef
6.
go back to reference Aller, S. G., et al. (2009). Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science, 323, 1718–1722.PubMedCrossRef Aller, S. G., et al. (2009). Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science, 323, 1718–1722.PubMedCrossRef
7.
go back to reference Fromm, M. F. (2004). Importance of P-glycoprotein at blood–tissue barriers. Trends in Pharmacological Sciences, 25, 423–429.PubMedCrossRef Fromm, M. F. (2004). Importance of P-glycoprotein at blood–tissue barriers. Trends in Pharmacological Sciences, 25, 423–429.PubMedCrossRef
8.
go back to reference Schinkel, A. H. (1997). The physiological function of drug-transporting P-glycoproteins. Seminars in Cancer Biology, 8, 161–170.PubMedCrossRef Schinkel, A. H. (1997). The physiological function of drug-transporting P-glycoproteins. Seminars in Cancer Biology, 8, 161–170.PubMedCrossRef
9.
go back to reference Sarkadi, B., Homolya, L., Szakacs, G., & Varadi, A. (2006). Human multidrug resistance ABCB and ABCG transporters: Participation in a chemoimmunity defense system. Physiological Reviews, 86, 1179–1236.PubMedCrossRef Sarkadi, B., Homolya, L., Szakacs, G., & Varadi, A. (2006). Human multidrug resistance ABCB and ABCG transporters: Participation in a chemoimmunity defense system. Physiological Reviews, 86, 1179–1236.PubMedCrossRef
10.
go back to reference Tainton, K. M., et al. (2004). Mutational analysis of P-glycoprotein: Suppression of caspase activation in the absence of ATP-dependent drug efflux. Cell Death and Differentiation, 11, 1028–1037.PubMedCrossRef Tainton, K. M., et al. (2004). Mutational analysis of P-glycoprotein: Suppression of caspase activation in the absence of ATP-dependent drug efflux. Cell Death and Differentiation, 11, 1028–1037.PubMedCrossRef
11.
go back to reference Pendse, S. S., et al. (2006). P-glycoprotein functions as a differentiation switch in antigen presenting cell maturation. American Journal of Transplantation, 6, 2884–2893.PubMedCrossRef Pendse, S. S., et al. (2006). P-glycoprotein functions as a differentiation switch in antigen presenting cell maturation. American Journal of Transplantation, 6, 2884–2893.PubMedCrossRef
12.
go back to reference Izawa, A., et al. (2010). A novel in vivo regulatory role of P-glycoprotein in alloimmunity. Biochemical and Biophysical Research Communications, 394, 646–652.PubMedCrossRef Izawa, A., et al. (2010). A novel in vivo regulatory role of P-glycoprotein in alloimmunity. Biochemical and Biophysical Research Communications, 394, 646–652.PubMedCrossRef
13.
go back to reference Cole, S. P., et al. (1992). Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. Science, 258, 1650–1654.PubMedCrossRef Cole, S. P., et al. (1992). Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. Science, 258, 1650–1654.PubMedCrossRef
14.
go back to reference Chen, Z. S., & Tiwari, A. K. (2011). Multidrug resistance proteins (MRPs/ABCCs) in cancer chemotherapy and genetic diseases. FEBS Journal, 278, 3226–3245.PubMedCrossRef Chen, Z. S., & Tiwari, A. K. (2011). Multidrug resistance proteins (MRPs/ABCCs) in cancer chemotherapy and genetic diseases. FEBS Journal, 278, 3226–3245.PubMedCrossRef
15.
go back to reference Wijnholds, J., et al. (2000). Multidrug resistance protein 1 protects the choroid plexus epithelium and contributes to the blood–cerebrospinal fluid barrier. The Journal of Clinical Investigation, 105, 279–285.PubMedCrossRef Wijnholds, J., et al. (2000). Multidrug resistance protein 1 protects the choroid plexus epithelium and contributes to the blood–cerebrospinal fluid barrier. The Journal of Clinical Investigation, 105, 279–285.PubMedCrossRef
16.
go back to reference van der Deen, M., et al. (2005). ATP-binding cassette (ABC) transporters in normal and pathological lung. Respiratory Research, 6, 59.PubMedCrossRef van der Deen, M., et al. (2005). ATP-binding cassette (ABC) transporters in normal and pathological lung. Respiratory Research, 6, 59.PubMedCrossRef
17.
go back to reference Nagashige, M., et al. (2003). Basal membrane localization of MRP1 in human placental trophoblast. Placenta, 24, 951–958.PubMedCrossRef Nagashige, M., et al. (2003). Basal membrane localization of MRP1 in human placental trophoblast. Placenta, 24, 951–958.PubMedCrossRef
18.
go back to reference Cole, S. P., & Deeley, R. G. (2006). Transport of glutathione and glutathione conjugates by MRP1. Trends in Pharmacological Sciences, 27, 438–446.PubMedCrossRef Cole, S. P., & Deeley, R. G. (2006). Transport of glutathione and glutathione conjugates by MRP1. Trends in Pharmacological Sciences, 27, 438–446.PubMedCrossRef
19.
go back to reference Renes, J., de Vries, E. G., Nienhuis, E. F., Jansen, P. L., & Muller, M. (1999). ATP- and glutathione-dependent transport of chemotherapeutic drugs by the multidrug resistance protein MRP1. British Journal of Pharmacology, 126, 681–688.PubMedCrossRef Renes, J., de Vries, E. G., Nienhuis, E. F., Jansen, P. L., & Muller, M. (1999). ATP- and glutathione-dependent transport of chemotherapeutic drugs by the multidrug resistance protein MRP1. British Journal of Pharmacology, 126, 681–688.PubMedCrossRef
20.
go back to reference Mueller, C. F., et al. (2005). The role of the multidrug resistance protein-1 in modulation of endothelial cell oxidative stress. Circulation Research, 97, 637–644.PubMedCrossRef Mueller, C. F., et al. (2005). The role of the multidrug resistance protein-1 in modulation of endothelial cell oxidative stress. Circulation Research, 97, 637–644.PubMedCrossRef
21.
go back to reference Wijnholds, J., et al. (1997). Increased sensitivity to anticancer drugs and decreased inflammatory response in mice lacking the multidrug resistance-associated protein. Nature Medicine, 3, 1275–1279.PubMedCrossRef Wijnholds, J., et al. (1997). Increased sensitivity to anticancer drugs and decreased inflammatory response in mice lacking the multidrug resistance-associated protein. Nature Medicine, 3, 1275–1279.PubMedCrossRef
22.
go back to reference Allen, J. D., Brinkhuis, R. F., van Deemter, L., Wijnholds, J., & Schinkel, A. H. (2000). Extensive contribution of the multidrug transporters P-glycoprotein and Mrp1 to basal drug resistance. Cancer Research, 60, 5761–5766.PubMed Allen, J. D., Brinkhuis, R. F., van Deemter, L., Wijnholds, J., & Schinkel, A. H. (2000). Extensive contribution of the multidrug transporters P-glycoprotein and Mrp1 to basal drug resistance. Cancer Research, 60, 5761–5766.PubMed
23.
go back to reference Keppler, D. (2011). Multidrug resistance proteins (MRPs, ABCCs): Importance for pathophysiology and drug therapy. Handbook of Experimental Pharmacology, 201, 299–323.PubMedCrossRef Keppler, D. (2011). Multidrug resistance proteins (MRPs, ABCCs): Importance for pathophysiology and drug therapy. Handbook of Experimental Pharmacology, 201, 299–323.PubMedCrossRef
24.
go back to reference Doyle, L. A., et al. (1998). A multidrug resistance transporter from human MCF-7 breast cancer cells. Proceedings of the National Academy of Sciences of the United States of America, 95, 15665–15670.PubMedCrossRef Doyle, L. A., et al. (1998). A multidrug resistance transporter from human MCF-7 breast cancer cells. Proceedings of the National Academy of Sciences of the United States of America, 95, 15665–15670.PubMedCrossRef
25.
go back to reference Ni, Z., Bikadi, Z., Rosenberg, M. F., & Mao, Q. (2010). Structure and function of the human breast cancer resistance protein (BCRP/ABCG2). Current Drug Metabolism, 11, 603–617.PubMedCrossRef Ni, Z., Bikadi, Z., Rosenberg, M. F., & Mao, Q. (2010). Structure and function of the human breast cancer resistance protein (BCRP/ABCG2). Current Drug Metabolism, 11, 603–617.PubMedCrossRef
26.
go back to reference van Herwaarden, A. E., et al. (2007). Multidrug transporter ABCG2/breast cancer resistance protein secretes riboflavin (vitamin B2) into milk. Molecular and Cellular Biology, 27, 1247–1253.PubMedCrossRef van Herwaarden, A. E., et al. (2007). Multidrug transporter ABCG2/breast cancer resistance protein secretes riboflavin (vitamin B2) into milk. Molecular and Cellular Biology, 27, 1247–1253.PubMedCrossRef
27.
go back to reference Assaraf, Y. G. (2006). The role of multidrug resistance efflux transporters in antifolate resistance and folate homeostasis. Drug Resistance Updates, 9, 227–246.PubMedCrossRef Assaraf, Y. G. (2006). The role of multidrug resistance efflux transporters in antifolate resistance and folate homeostasis. Drug Resistance Updates, 9, 227–246.PubMedCrossRef
28.
go back to reference Suzuki, M., Suzuki, H., Sugimoto, Y., & Sugiyama, Y. (2003). ABCG2 transports sulfated conjugates of steroids and xenobiotics. Journal of Biological Chemistry, 278, 22644–22649.PubMedCrossRef Suzuki, M., Suzuki, H., Sugimoto, Y., & Sugiyama, Y. (2003). ABCG2 transports sulfated conjugates of steroids and xenobiotics. Journal of Biological Chemistry, 278, 22644–22649.PubMedCrossRef
29.
go back to reference Redmond, K. M., Wilson, T. R., Johnston, P. G., & Longley, D. B. (2008). Resistance mechanisms to cancer chemotherapy. Frontiers in Bioscience, 13, 5138–5154.PubMedCrossRef Redmond, K. M., Wilson, T. R., Johnston, P. G., & Longley, D. B. (2008). Resistance mechanisms to cancer chemotherapy. Frontiers in Bioscience, 13, 5138–5154.PubMedCrossRef
30.
go back to reference Leith, C. P., et al. (1997). Acute myeloid leukemia in the elderly: Assessment of multidrug resistance (MDR1) and cytogenetics distinguishes biologic subgroups with remarkably distinct responses to standard chemotherapy. A Southwest Oncology Group study. Blood, 89, 3323–3329.PubMed Leith, C. P., et al. (1997). Acute myeloid leukemia in the elderly: Assessment of multidrug resistance (MDR1) and cytogenetics distinguishes biologic subgroups with remarkably distinct responses to standard chemotherapy. A Southwest Oncology Group study. Blood, 89, 3323–3329.PubMed
31.
go back to reference van den Heuvel-Eibrink, M. M., et al. (1997). MDR 1 expression is an independent prognostic factor for response and survival in de novo acute myeloid leukaemia. British Journal of Haematology, 99, 76–83.PubMedCrossRef van den Heuvel-Eibrink, M. M., et al. (1997). MDR 1 expression is an independent prognostic factor for response and survival in de novo acute myeloid leukaemia. British Journal of Haematology, 99, 76–83.PubMedCrossRef
32.
go back to reference Burger, H., et al. (2003). RNA expression of breast cancer resistance protein, lung resistance-related protein, multidrug resistance-associated proteins 1 and 2, and multidrug resistance gene 1 in breast cancer: Correlation with chemotherapeutic response. Clinical Cancer Research, 9, 827–836.PubMed Burger, H., et al. (2003). RNA expression of breast cancer resistance protein, lung resistance-related protein, multidrug resistance-associated proteins 1 and 2, and multidrug resistance gene 1 in breast cancer: Correlation with chemotherapeutic response. Clinical Cancer Research, 9, 827–836.PubMed
33.
go back to reference Chan, H. S., Grogan, T. M., Haddad, G., DeBoer, G., & Ling, V. (1997). P-glycoprotein expression: Critical determinant in the response to osteosarcoma chemotherapy. Journal of the National Cancer Institute, 89, 1706–1715.PubMedCrossRef Chan, H. S., Grogan, T. M., Haddad, G., DeBoer, G., & Ling, V. (1997). P-glycoprotein expression: Critical determinant in the response to osteosarcoma chemotherapy. Journal of the National Cancer Institute, 89, 1706–1715.PubMedCrossRef
34.
go back to reference Trock, B. J., Leonessa, F., & Clarke, R. (1997). Multidrug resistance in breast cancer: A meta-analysis of MDR1/gp170 expression and its possible functional significance. Journal of the National Cancer Institute, 89, 917–931.PubMedCrossRef Trock, B. J., Leonessa, F., & Clarke, R. (1997). Multidrug resistance in breast cancer: A meta-analysis of MDR1/gp170 expression and its possible functional significance. Journal of the National Cancer Institute, 89, 917–931.PubMedCrossRef
35.
go back to reference Zhou, D. C., Zittoun, R., & Marie, J. P. (1995). Expression of multidrug resistance-associated protein (MRP) and multidrug resistance (MDR1) genes in acute myeloid leukemia. Leukemia, 9, 1661–1666.PubMed Zhou, D. C., Zittoun, R., & Marie, J. P. (1995). Expression of multidrug resistance-associated protein (MRP) and multidrug resistance (MDR1) genes in acute myeloid leukemia. Leukemia, 9, 1661–1666.PubMed
36.
go back to reference Grogan, T. M., et al. (1993). P-glycoprotein expression in human plasma cell myeloma: Correlation with prior chemotherapy. Blood, 81, 490–495.PubMed Grogan, T. M., et al. (1993). P-glycoprotein expression in human plasma cell myeloma: Correlation with prior chemotherapy. Blood, 81, 490–495.PubMed
37.
go back to reference Chevillard, S., et al. (1996). Sequential assessment of multidrug resistance phenotype and measurement of S-phase fraction as predictive markers of breast cancer response to neoadjuvant chemotherapy. Cancer, 77, 292–300.PubMedCrossRef Chevillard, S., et al. (1996). Sequential assessment of multidrug resistance phenotype and measurement of S-phase fraction as predictive markers of breast cancer response to neoadjuvant chemotherapy. Cancer, 77, 292–300.PubMedCrossRef
38.
go back to reference Kimura, Y., et al. (2002). P-glycoprotein inhibition by the multidrug resistance-reversing agent MS-209 enhances bioavailability and antitumor efficacy of orally administered paclitaxel. Cancer Chemotherapy and Pharmacology, 49, 322–328.PubMedCrossRef Kimura, Y., et al. (2002). P-glycoprotein inhibition by the multidrug resistance-reversing agent MS-209 enhances bioavailability and antitumor efficacy of orally administered paclitaxel. Cancer Chemotherapy and Pharmacology, 49, 322–328.PubMedCrossRef
39.
go back to reference Hyafil, F., Vergely, C., Du Vignaud, P., & Grand-Perret, T. (1993). In vitro and in vivo reversal of multidrug resistance by GF120918, an acridonecarboxamide derivative. Cancer Research, 53, 4595–4602.PubMed Hyafil, F., Vergely, C., Du Vignaud, P., & Grand-Perret, T. (1993). In vitro and in vivo reversal of multidrug resistance by GF120918, an acridonecarboxamide derivative. Cancer Research, 53, 4595–4602.PubMed
40.
go back to reference Dantzig, A. H., et al. (1996). Reversal of P-glycoprotein-mediated multidrug resistance by a potent cyclopropyldibenzosuberane modulator, LY335979. Cancer Research, 56, 4171–4179.PubMed Dantzig, A. H., et al. (1996). Reversal of P-glycoprotein-mediated multidrug resistance by a potent cyclopropyldibenzosuberane modulator, LY335979. Cancer Research, 56, 4171–4179.PubMed
41.
go back to reference Pajic, M., et al. (2009). Moderate increase in Mdr1a/1b expression causes in vivo resistance to doxorubicin in a mouse model for hereditary breast cancer. Cancer Research, 69, 6396–6404.PubMedCrossRef Pajic, M., et al. (2009). Moderate increase in Mdr1a/1b expression causes in vivo resistance to doxorubicin in a mouse model for hereditary breast cancer. Cancer Research, 69, 6396–6404.PubMedCrossRef
42.
go back to reference Mistry, P., et al. (2001). In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576. Cancer Research, 61, 749–758.PubMed Mistry, P., et al. (2001). In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576. Cancer Research, 61, 749–758.PubMed
43.
go back to reference Naito, M., Matsuba, Y., Sato, S., Hirata, H., & Tsuruo, T. (2002). MS-209, a quinoline-type reversal agent, potentiates antitumor efficacy of docetaxel in multidrug-resistant solid tumor xenograft models. Clinical Cancer Research, 8, 582–588.PubMed Naito, M., Matsuba, Y., Sato, S., Hirata, H., & Tsuruo, T. (2002). MS-209, a quinoline-type reversal agent, potentiates antitumor efficacy of docetaxel in multidrug-resistant solid tumor xenograft models. Clinical Cancer Research, 8, 582–588.PubMed
44.
go back to reference McDevitt, C. A., & Callaghan, R. (2007). How can we best use structural information on P-glycoprotein to design inhibitors? Pharmacology and Therapeutics, 113, 429–441.PubMedCrossRef McDevitt, C. A., & Callaghan, R. (2007). How can we best use structural information on P-glycoprotein to design inhibitors? Pharmacology and Therapeutics, 113, 429–441.PubMedCrossRef
45.
go back to reference Solary, E., et al. (2003). Quinine as a multidrug resistance inhibitor: A phase 3 multicentric randomized study in adult de novo acute myelogenous leukemia. Blood, 102, 1202–1210.PubMedCrossRef Solary, E., et al. (2003). Quinine as a multidrug resistance inhibitor: A phase 3 multicentric randomized study in adult de novo acute myelogenous leukemia. Blood, 102, 1202–1210.PubMedCrossRef
46.
go back to reference Solary, E., et al. (1996). Combination of quinine as a potential reversing agent with mitoxantrone and cytarabine for the treatment of acute leukemias: A randomized multicenter study. Blood, 88, 1198–1205.PubMed Solary, E., et al. (1996). Combination of quinine as a potential reversing agent with mitoxantrone and cytarabine for the treatment of acute leukemias: A randomized multicenter study. Blood, 88, 1198–1205.PubMed
47.
go back to reference Ozols, R. F., et al. (1987). Verapamil and adriamycin in the treatment of drug-resistant ovarian cancer patients. Journal of Clinical Oncology, 5, 641–647.PubMed Ozols, R. F., et al. (1987). Verapamil and adriamycin in the treatment of drug-resistant ovarian cancer patients. Journal of Clinical Oncology, 5, 641–647.PubMed
48.
go back to reference Millward, M. J., et al. (1993). Oral verapamil with chemotherapy for advanced non-small cell lung cancer: A randomised study. British Journal of Cancer, 67, 1031–1035.PubMedCrossRef Millward, M. J., et al. (1993). Oral verapamil with chemotherapy for advanced non-small cell lung cancer: A randomised study. British Journal of Cancer, 67, 1031–1035.PubMedCrossRef
49.
go back to reference Milroy, R. (1993). A randomised clinical study of verapamil in addition to combination chemotherapy in small cell lung cancer. West of Scotland Lung Cancer Research Group, and the Aberdeen Oncology Group. British Journal of Cancer, 68, 813–818.PubMedCrossRef Milroy, R. (1993). A randomised clinical study of verapamil in addition to combination chemotherapy in small cell lung cancer. West of Scotland Lung Cancer Research Group, and the Aberdeen Oncology Group. British Journal of Cancer, 68, 813–818.PubMedCrossRef
50.
go back to reference Chico, I., et al. (2001). Phase I study of infusional paclitaxel in combination with the P-glycoprotein antagonist PSC 833. Journal of Clinical Oncology, 19, 832–842.PubMed Chico, I., et al. (2001). Phase I study of infusional paclitaxel in combination with the P-glycoprotein antagonist PSC 833. Journal of Clinical Oncology, 19, 832–842.PubMed
51.
go back to reference Baer, M. R., et al. (2002). Phase 3 study of the multidrug resistance modulator PSC-833 in previously untreated patients 60 years of age and older with acute myeloid leukemia: Cancer and Leukemia Group B Study 9720. Blood, 100, 1224–1232.PubMed Baer, M. R., et al. (2002). Phase 3 study of the multidrug resistance modulator PSC-833 in previously untreated patients 60 years of age and older with acute myeloid leukemia: Cancer and Leukemia Group B Study 9720. Blood, 100, 1224–1232.PubMed
52.
go back to reference Saeki, T., et al. (2007). Dofequidar fumarate (MS-209) in combination with cyclophosphamide, doxorubicin, and fluorouracil for patients with advanced or recurrent breast cancer. Journal of Clinical Oncology, 25, 411–417.PubMedCrossRef Saeki, T., et al. (2007). Dofequidar fumarate (MS-209) in combination with cyclophosphamide, doxorubicin, and fluorouracil for patients with advanced or recurrent breast cancer. Journal of Clinical Oncology, 25, 411–417.PubMedCrossRef
53.
go back to reference Germann, U. A., et al. (1997). Cellular and biochemical characterization of VX-710 as a chemosensitizer: Reversal of P-glycoprotein-mediated multidrug resistance in vitro. Anti-Cancer Drugs, 8, 125–140.PubMedCrossRef Germann, U. A., et al. (1997). Cellular and biochemical characterization of VX-710 as a chemosensitizer: Reversal of P-glycoprotein-mediated multidrug resistance in vitro. Anti-Cancer Drugs, 8, 125–140.PubMedCrossRef
54.
go back to reference Minderman, H., O’Loughlin, K. L., Pendyala, L., & Baer, M. R. (2004). VX-710 (biricodar) increases drug retention and enhances chemosensitivity in resistant cells overexpressing P-glycoprotein, multidrug resistance protein, and breast cancer resistance protein. Clinical Cancer Research, 10, 1826–1834.PubMedCrossRef Minderman, H., O’Loughlin, K. L., Pendyala, L., & Baer, M. R. (2004). VX-710 (biricodar) increases drug retention and enhances chemosensitivity in resistant cells overexpressing P-glycoprotein, multidrug resistance protein, and breast cancer resistance protein. Clinical Cancer Research, 10, 1826–1834.PubMedCrossRef
55.
go back to reference Gandhi, L., et al. (2007). A phase II study of the safety and efficacy of the multidrug resistance inhibitor VX-710 combined with doxorubicin and vincristine in patients with recurrent small cell lung cancer. Cancer, 109, 924–932.PubMedCrossRef Gandhi, L., et al. (2007). A phase II study of the safety and efficacy of the multidrug resistance inhibitor VX-710 combined with doxorubicin and vincristine in patients with recurrent small cell lung cancer. Cancer, 109, 924–932.PubMedCrossRef
56.
go back to reference Hubensack, M., et al. (2008). Effect of the ABCB1 modulators elacridar and tariquidar on the distribution of paclitaxel in nude mice. Journal of Cancer Research and Clinical Oncology, 134, 597–607.PubMedCrossRef Hubensack, M., et al. (2008). Effect of the ABCB1 modulators elacridar and tariquidar on the distribution of paclitaxel in nude mice. Journal of Cancer Research and Clinical Oncology, 134, 597–607.PubMedCrossRef
57.
go back to reference Jonker, J. W., et al. (2000). Role of breast cancer resistance protein in the bioavailability and fetal penetration of topotecan. Journal of the National Cancer Institute, 92, 1651–1656.PubMedCrossRef Jonker, J. W., et al. (2000). Role of breast cancer resistance protein in the bioavailability and fetal penetration of topotecan. Journal of the National Cancer Institute, 92, 1651–1656.PubMedCrossRef
58.
go back to reference Kruijtzer, C. M., et al. (2002). Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918. Journal of Clinical Oncology, 20, 2943–2950.PubMedCrossRef Kruijtzer, C. M., et al. (2002). Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918. Journal of Clinical Oncology, 20, 2943–2950.PubMedCrossRef
59.
go back to reference Kuppens, I. E., et al. (2007). A phase I, randomized, open-label, parallel-cohort, dose-finding study of elacridar (GF120918) and oral topotecan in cancer patients. Clinical Cancer Research, 13, 3276–3285.PubMedCrossRef Kuppens, I. E., et al. (2007). A phase I, randomized, open-label, parallel-cohort, dose-finding study of elacridar (GF120918) and oral topotecan in cancer patients. Clinical Cancer Research, 13, 3276–3285.PubMedCrossRef
60.
go back to reference Gerrard, G., et al. (2004). Clinical effects and P-glycoprotein inhibition in patients with acute myeloid leukemia treated with zosuquidar trihydrochloride, daunorubicin and cytarabine. Haematologica, 89, 782–790.PubMed Gerrard, G., et al. (2004). Clinical effects and P-glycoprotein inhibition in patients with acute myeloid leukemia treated with zosuquidar trihydrochloride, daunorubicin and cytarabine. Haematologica, 89, 782–790.PubMed
61.
go back to reference Morschhauser, F., et al. (2007). Phase I/II trial of a P-glycoprotein inhibitor, Zosuquidar.3HCl trihydrochloride (LY335979), given orally in combination with the CHOP regimen in patients with non-Hodgkin’s lymphoma. Leukemia & Lymphoma, 48, 708–715.CrossRef Morschhauser, F., et al. (2007). Phase I/II trial of a P-glycoprotein inhibitor, Zosuquidar.3HCl trihydrochloride (LY335979), given orally in combination with the CHOP regimen in patients with non-Hodgkin’s lymphoma. Leukemia & Lymphoma, 48, 708–715.CrossRef
62.
go back to reference Cripe, L. D., et al. (2010). Zosuquidar, a novel modulator of P-glycoprotein, does not improve the outcome of older patients with newly diagnosed acute myeloid leukemia: A randomized, placebo-controlled trial of the Eastern Cooperative Oncology Group 3999. Blood, 116, 4077–4085.PubMedCrossRef Cripe, L. D., et al. (2010). Zosuquidar, a novel modulator of P-glycoprotein, does not improve the outcome of older patients with newly diagnosed acute myeloid leukemia: A randomized, placebo-controlled trial of the Eastern Cooperative Oncology Group 3999. Blood, 116, 4077–4085.PubMedCrossRef
63.
go back to reference Pusztai, L., et al. (2005). Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma. Cancer, 104, 682–691.PubMedCrossRef Pusztai, L., et al. (2005). Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma. Cancer, 104, 682–691.PubMedCrossRef
64.
go back to reference Fox, E., & Bates, S. E. (2007). Tariquidar (XR9576): A P-glycoprotein drug efflux pump inhibitor. Expert Review of Anticancer Therapy, 7, 447–459.PubMedCrossRef Fox, E., & Bates, S. E. (2007). Tariquidar (XR9576): A P-glycoprotein drug efflux pump inhibitor. Expert Review of Anticancer Therapy, 7, 447–459.PubMedCrossRef
65.
go back to reference Ferguson, P. J., Brisson, A. R., Koropatnick, J., & Vincent, M. D. (2009). Enhancement of cytotoxicity of natural product drugs against multidrug resistant variant cell lines of human head and neck squamous cell carcinoma and breast carcinoma by tesmilifene. Cancer Letters, 274, 279–289.PubMedCrossRef Ferguson, P. J., Brisson, A. R., Koropatnick, J., & Vincent, M. D. (2009). Enhancement of cytotoxicity of natural product drugs against multidrug resistant variant cell lines of human head and neck squamous cell carcinoma and breast carcinoma by tesmilifene. Cancer Letters, 274, 279–289.PubMedCrossRef
66.
go back to reference Vincent, M. (2006). Tesmilifene may enhance breast cancer chemotherapy by killing a clone of aggressive, multi-drug resistant cells through its action on the p-glycoprotein pump. Medical Hypotheses, 66, 715–731.PubMedCrossRef Vincent, M. (2006). Tesmilifene may enhance breast cancer chemotherapy by killing a clone of aggressive, multi-drug resistant cells through its action on the p-glycoprotein pump. Medical Hypotheses, 66, 715–731.PubMedCrossRef
67.
go back to reference Reyno, L., et al. (2004). Phase III study of N,N-diethyl-2-[4-(phenylmethyl) phenoxy]ethanamine (BMS-217380-01) combined with doxorubicin versus doxorubicin alone in metastatic/recurrent breast cancer: National Cancer Institute of Canada Clinical Trials Group Study MA.19. Journal of Clinical Oncology, 22, 269–276.PubMedCrossRef Reyno, L., et al. (2004). Phase III study of N,N-diethyl-2-[4-(phenylmethyl) phenoxy]ethanamine (BMS-217380-01) combined with doxorubicin versus doxorubicin alone in metastatic/recurrent breast cancer: National Cancer Institute of Canada Clinical Trials Group Study MA.19. Journal of Clinical Oncology, 22, 269–276.PubMedCrossRef
68.
go back to reference Robey, R. W., et al. (2008). Inhibition of P-glycoprotein (ABCB1)- and multidrug resistance-associated protein 1 (ABCC1)-mediated transport by the orally administered inhibitor, CBT-1((R)). Biochemical Pharmacology, 75, 1302–1312.PubMedCrossRef Robey, R. W., et al. (2008). Inhibition of P-glycoprotein (ABCB1)- and multidrug resistance-associated protein 1 (ABCC1)-mediated transport by the orally administered inhibitor, CBT-1((R)). Biochemical Pharmacology, 75, 1302–1312.PubMedCrossRef
69.
go back to reference Oldham, R. K., Reid, W. K., Preisler, H. D., & Barnett, D. (1998). A phase I and pharmacokinetic study of CBT-1 as a multidrug resistance modulator in the treatment of patients with advanced cancer. Cancer Biotherapy & Radiopharmaceuticals, 13, 71–80.CrossRef Oldham, R. K., Reid, W. K., Preisler, H. D., & Barnett, D. (1998). A phase I and pharmacokinetic study of CBT-1 as a multidrug resistance modulator in the treatment of patients with advanced cancer. Cancer Biotherapy & Radiopharmaceuticals, 13, 71–80.CrossRef
70.
go back to reference Kelly R.J., et al. (2012). A pharmacodynamic study of the P-glycoprotein antagonist CBT-1(R) in combination with paclitaxel in solid tumors. Oncologist, 17(4), 512. Kelly R.J., et al. (2012). A pharmacodynamic study of the P-glycoprotein antagonist CBT-1(R) in combination with paclitaxel in solid tumors. Oncologist, 17(4), 512.
71.
go back to reference Popoli, P., Pezzola, A., Benedetti, M., & Scotti de Carolis, A. (1992). Verapamil and flunarizine inhibit phencyclidine-induced effects: An EEG and behavioural study in rats. Neuropharmacology, 31, 1185–1191.PubMedCrossRef Popoli, P., Pezzola, A., Benedetti, M., & Scotti de Carolis, A. (1992). Verapamil and flunarizine inhibit phencyclidine-induced effects: An EEG and behavioural study in rats. Neuropharmacology, 31, 1185–1191.PubMedCrossRef
72.
go back to reference Akimoto, H., et al. (1993). Effect of verapamil on doxorubicin cardiotoxicity: Altered muscle gene expression in cultured neonatal rat cardiomyocytes. Cancer Research, 53, 4658–4664.PubMed Akimoto, H., et al. (1993). Effect of verapamil on doxorubicin cardiotoxicity: Altered muscle gene expression in cultured neonatal rat cardiomyocytes. Cancer Research, 53, 4658–4664.PubMed
73.
go back to reference Borel, J. F., et al. (1996). In vivo pharmacological effects of ciclosporin and some analogues. Advances in Pharmacology, 35, 115–246.PubMedCrossRef Borel, J. F., et al. (1996). In vivo pharmacological effects of ciclosporin and some analogues. Advances in Pharmacology, 35, 115–246.PubMedCrossRef
74.
go back to reference Kim, R. B., et al. (1999). Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharmaceutical Research, 16, 408–414.PubMedCrossRef Kim, R. B., et al. (1999). Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharmaceutical Research, 16, 408–414.PubMedCrossRef
75.
go back to reference Patel, J., & Mitra, A. K. (2001). Strategies to overcome simultaneous P-glycoprotein mediated efflux and CYP3A4 mediated metabolism of drugs. Pharmacogenomics, 2, 401–415.PubMedCrossRef Patel, J., & Mitra, A. K. (2001). Strategies to overcome simultaneous P-glycoprotein mediated efflux and CYP3A4 mediated metabolism of drugs. Pharmacogenomics, 2, 401–415.PubMedCrossRef
76.
go back to reference Eckford, P. D., & Sharom, F. J. (2009). ABC efflux pump-based resistance to chemotherapy drugs. Chemical Reviews, 109, 2989–3011.PubMedCrossRef Eckford, P. D., & Sharom, F. J. (2009). ABC efflux pump-based resistance to chemotherapy drugs. Chemical Reviews, 109, 2989–3011.PubMedCrossRef
77.
go back to reference Roy, S., et al. (2007). MDR1/P-glycoprotein and MRP-1 mRNA and protein expression in non-small cell lung cancer. Anticancer Research, 27, 1325–1330.PubMed Roy, S., et al. (2007). MDR1/P-glycoprotein and MRP-1 mRNA and protein expression in non-small cell lung cancer. Anticancer Research, 27, 1325–1330.PubMed
78.
go back to reference Li, J., et al. (2009). Expression of MRP1, BCRP, LRP, and ERCC1 in advanced non-small-cell lung cancer: Correlation with response to chemotherapy and survival. Clinical Lung Cancer, 10, 414–421.PubMedCrossRef Li, J., et al. (2009). Expression of MRP1, BCRP, LRP, and ERCC1 in advanced non-small-cell lung cancer: Correlation with response to chemotherapy and survival. Clinical Lung Cancer, 10, 414–421.PubMedCrossRef
79.
go back to reference Robey, R. W., et al. (2004). Pheophorbide a is a specific probe for ABCG2 function and inhibition. Cancer Research, 64, 1242–1246.PubMedCrossRef Robey, R. W., et al. (2004). Pheophorbide a is a specific probe for ABCG2 function and inhibition. Cancer Research, 64, 1242–1246.PubMedCrossRef
80.
go back to reference Hoffmeyer, S., et al. (2000). Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proceedings of the National Academy of Sciences of the United States of America, 97, 3473–3478.PubMedCrossRef Hoffmeyer, S., et al. (2000). Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proceedings of the National Academy of Sciences of the United States of America, 97, 3473–3478.PubMedCrossRef
81.
go back to reference Ozawa, S., et al. (2004). Ethnic differences in genetic polymorphisms of CYP2D6, CYP2C19, CYP3As and MDR1/ABCB1. Drug Metabolism and Pharmacokinetics, 19, 83–95.PubMedCrossRef Ozawa, S., et al. (2004). Ethnic differences in genetic polymorphisms of CYP2D6, CYP2C19, CYP3As and MDR1/ABCB1. Drug Metabolism and Pharmacokinetics, 19, 83–95.PubMedCrossRef
82.
go back to reference Cascorbi, I. (2006). Role of pharmacogenetics of ATP-binding cassette transporters in the pharmacokinetics of drugs. Pharmacology and Therapeutics, 112, 457–473.PubMedCrossRef Cascorbi, I. (2006). Role of pharmacogenetics of ATP-binding cassette transporters in the pharmacokinetics of drugs. Pharmacology and Therapeutics, 112, 457–473.PubMedCrossRef
83.
go back to reference Kimchi-Sarfaty, C., et al. (2007). A “silent” polymorphism in the MDR1 gene changes substrate specificity. Science, 315, 525–528.PubMedCrossRef Kimchi-Sarfaty, C., et al. (2007). A “silent” polymorphism in the MDR1 gene changes substrate specificity. Science, 315, 525–528.PubMedCrossRef
84.
go back to reference Crouthamel, M. H., Wu, D., Yang, Z., & Ho, R. J. (2010). A novel MDR1 GT1292-3TG (Cys431Leu) genetic variation and its effect on P-glycoprotein biologic functions. The AAPS Journal, 12, 548–555.PubMedCrossRef Crouthamel, M. H., Wu, D., Yang, Z., & Ho, R. J. (2010). A novel MDR1 GT1292-3TG (Cys431Leu) genetic variation and its effect on P-glycoprotein biologic functions. The AAPS Journal, 12, 548–555.PubMedCrossRef
85.
go back to reference Sakaeda, T. (2005). MDR1 genotype-related pharmacokinetics: Fact or fiction? Drug Metabolism and Pharmacokinetics, 20, 391–414.PubMedCrossRef Sakaeda, T. (2005). MDR1 genotype-related pharmacokinetics: Fact or fiction? Drug Metabolism and Pharmacokinetics, 20, 391–414.PubMedCrossRef
86.
go back to reference Cascorbi I. (2011). P-glycoprotein: Tissue distribution, substrates, and functional consequences of genetic variations. Handbook of Experimental Pharmacology, (201), 261–283. Cascorbi I. (2011). P-glycoprotein: Tissue distribution, substrates, and functional consequences of genetic variations. Handbook of Experimental Pharmacology, (201), 261–283.
87.
go back to reference Mathijssen, R. H., et al. (2003). Irinotecan pathway genotype analysis to predict pharmacokinetics. Clinical Cancer Research, 9, 3246–3253.PubMed Mathijssen, R. H., et al. (2003). Irinotecan pathway genotype analysis to predict pharmacokinetics. Clinical Cancer Research, 9, 3246–3253.PubMed
88.
go back to reference Kafka, A., et al. (2003). Polymorphism C3435T of the MDR-1 gene predicts response to preoperative chemotherapy in locally advanced breast cancer. International Journal of Oncology, 22, 1117–1121.PubMed Kafka, A., et al. (2003). Polymorphism C3435T of the MDR-1 gene predicts response to preoperative chemotherapy in locally advanced breast cancer. International Journal of Oncology, 22, 1117–1121.PubMed
89.
go back to reference Green, H., Soderkvist, P., Rosenberg, P., Horvath, G., & Peterson, C. (2008). ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel. Journal of Pharmaceutical Sciences, 97, 2045–2048.PubMedCrossRef Green, H., Soderkvist, P., Rosenberg, P., Horvath, G., & Peterson, C. (2008). ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel. Journal of Pharmaceutical Sciences, 97, 2045–2048.PubMedCrossRef
90.
go back to reference Trédan, O., Galmarini, C. M., Patel, K., & Tannock, I. F. (2007). Drug resistance and the solid tumor microenvironment. Journal of the National Cancer Institute, 99, 1441–1454.PubMedCrossRef Trédan, O., Galmarini, C. M., Patel, K., & Tannock, I. F. (2007). Drug resistance and the solid tumor microenvironment. Journal of the National Cancer Institute, 99, 1441–1454.PubMedCrossRef
91.
go back to reference Tunggal, J. K., Melo, T., Ballinger, J. R., & Tannock, I. F. (2000). The influence of expression of P-glycoprotein on the penetration of anticancer drugs through multicellular layers. International Journal of Cancer, 86, 101–107.CrossRef Tunggal, J. K., Melo, T., Ballinger, J. R., & Tannock, I. F. (2000). The influence of expression of P-glycoprotein on the penetration of anticancer drugs through multicellular layers. International Journal of Cancer, 86, 101–107.CrossRef
92.
go back to reference Patel, K. J., & Tannock, I. F. (2009). The influence of P-glycoprotein expression and its inhibitors on the distribution of doxorubicin in breast tumors. BMC Cancer, 9, 356.PubMedCrossRef Patel, K. J., & Tannock, I. F. (2009). The influence of P-glycoprotein expression and its inhibitors on the distribution of doxorubicin in breast tumors. BMC Cancer, 9, 356.PubMedCrossRef
93.
go back to reference Huxham, L. A., Kyle, A. H., Baker, J. H., Nykilchuk, L. K., & Minchinton, A. I. (2004). Microregional effects of gemcitabine in HCT-116 xenografts. Cancer Research, 64, 6537–6541.PubMedCrossRef Huxham, L. A., Kyle, A. H., Baker, J. H., Nykilchuk, L. K., & Minchinton, A. I. (2004). Microregional effects of gemcitabine in HCT-116 xenografts. Cancer Research, 64, 6537–6541.PubMedCrossRef
94.
go back to reference Tunggal, J. K., Ballinger, J. R., & Tannock, I. F. (1999). Influence of cell concentration in limiting the therapeutic benefit of P-glycoprotein reversal agents. International Journal of Cancer, 81, 741–747.CrossRef Tunggal, J. K., Ballinger, J. R., & Tannock, I. F. (1999). Influence of cell concentration in limiting the therapeutic benefit of P-glycoprotein reversal agents. International Journal of Cancer, 81, 741–747.CrossRef
95.
go back to reference Shi, T., Wrin, J., Reeder, J., Liu, D., & Ring, D. B. (1995). High-affinity monoclonal antibodies against P-glycoprotein. Clinical Immunology and Immunopathology, 76, 44–51.PubMedCrossRef Shi, T., Wrin, J., Reeder, J., Liu, D., & Ring, D. B. (1995). High-affinity monoclonal antibodies against P-glycoprotein. Clinical Immunology and Immunopathology, 76, 44–51.PubMedCrossRef
96.
go back to reference Nobili S., Landini I., Mazzei T., & Mini E. (2012). Overcoming tumor multidrug resistance using drugs able to evade P-glycoprotein or to exploit its expression. Medicinal Research Reviews, 32, 1220–1262. Nobili S., Landini I., Mazzei T., & Mini E. (2012). Overcoming tumor multidrug resistance using drugs able to evade P-glycoprotein or to exploit its expression. Medicinal Research Reviews, 32, 1220–1262.
97.
go back to reference McLachlin, J. R., et al. (1990). Expression of a human complementary DNA for the multidrug resistance gene in murine hematopoietic precursor cells with the use of retroviral gene transfer. Journal of the National Cancer Institute, 82, 1260–1263.PubMedCrossRef McLachlin, J. R., et al. (1990). Expression of a human complementary DNA for the multidrug resistance gene in murine hematopoietic precursor cells with the use of retroviral gene transfer. Journal of the National Cancer Institute, 82, 1260–1263.PubMedCrossRef
98.
go back to reference Mickisch, G. H., Merlino, G. T., Galski, H., Gottesman, M. M., & Pastan, I. (1991). Transgenic mice that express the human multidrug-resistance gene in bone marrow enable a rapid identification of agents that reverse drug resistance. Proceedings of the National Academy of Sciences of the United States of America, 88, 547–551.PubMedCrossRef Mickisch, G. H., Merlino, G. T., Galski, H., Gottesman, M. M., & Pastan, I. (1991). Transgenic mice that express the human multidrug-resistance gene in bone marrow enable a rapid identification of agents that reverse drug resistance. Proceedings of the National Academy of Sciences of the United States of America, 88, 547–551.PubMedCrossRef
99.
go back to reference Hesdorffer, C., et al. (1998). Phase I trial of retroviral-mediated transfer of the human MDR1 gene as marrow chemoprotection in patients undergoing high-dose chemotherapy and autologous stem-cell transplantation. Journal of Clinical Oncology, 16, 165–172.PubMed Hesdorffer, C., et al. (1998). Phase I trial of retroviral-mediated transfer of the human MDR1 gene as marrow chemoprotection in patients undergoing high-dose chemotherapy and autologous stem-cell transplantation. Journal of Clinical Oncology, 16, 165–172.PubMed
100.
go back to reference Iwahashi, T., et al. (1993). Specific targeting and killing activities of anti-P-glycoprotein monoclonal antibody MRK16 directed against intrinsically multidrug-resistant human colorectal carcinoma cell lines in the nude mouse model. Cancer Research, 53, 5475–5482.PubMed Iwahashi, T., et al. (1993). Specific targeting and killing activities of anti-P-glycoprotein monoclonal antibody MRK16 directed against intrinsically multidrug-resistant human colorectal carcinoma cell lines in the nude mouse model. Cancer Research, 53, 5475–5482.PubMed
101.
go back to reference Mechetner, E. B., & Roninson, I. B. (1992). Efficient inhibition of P-glycoprotein-mediated multidrug resistance with a monoclonal antibody. Proceedings of the National Academy of Sciences of the United States of America, 89, 5824–5828.PubMedCrossRef Mechetner, E. B., & Roninson, I. B. (1992). Efficient inhibition of P-glycoprotein-mediated multidrug resistance with a monoclonal antibody. Proceedings of the National Academy of Sciences of the United States of America, 89, 5824–5828.PubMedCrossRef
102.
go back to reference Mickisch, G. H., Pai, L. H., Gottesman, M. M., & Pastan, I. (1992). Monoclonal antibody MRK16 reverses the multidrug resistance of multidrug-resistant transgenic mice. Cancer Research, 52, 4427–4432.PubMed Mickisch, G. H., Pai, L. H., Gottesman, M. M., & Pastan, I. (1992). Monoclonal antibody MRK16 reverses the multidrug resistance of multidrug-resistant transgenic mice. Cancer Research, 52, 4427–4432.PubMed
103.
go back to reference Rittmann-Grauer, L. S., Yong, M. A., Sanders, V., & Mackensen, D. G. (1992). Reversal of Vinca alkaloid resistance by anti-P-glycoprotein monoclonal antibody HYB-241 in a human tumor xenograft. Cancer Research, 52, 1810–1816.PubMed Rittmann-Grauer, L. S., Yong, M. A., Sanders, V., & Mackensen, D. G. (1992). Reversal of Vinca alkaloid resistance by anti-P-glycoprotein monoclonal antibody HYB-241 in a human tumor xenograft. Cancer Research, 52, 1810–1816.PubMed
104.
go back to reference Goda, K., et al. (2007). Complete inhibition of P-glycoprotein by simultaneous treatment with a distinct class of modulators and the UIC2 monoclonal antibody. Journal of Pharmacology and Experimental Therapeutics, 320, 81–88.PubMedCrossRef Goda, K., et al. (2007). Complete inhibition of P-glycoprotein by simultaneous treatment with a distinct class of modulators and the UIC2 monoclonal antibody. Journal of Pharmacology and Experimental Therapeutics, 320, 81–88.PubMedCrossRef
105.
go back to reference Krasznai, Z. T., et al. (2010). Pgp inhibition by UIC2 antibody can be followed in vitro by using tumor-diagnostic radiotracers, 99mTc-MIBI and 18FDG. European Journal of Pharmaceutical Sciences, 41, 665–669.PubMedCrossRef Krasznai, Z. T., et al. (2010). Pgp inhibition by UIC2 antibody can be followed in vitro by using tumor-diagnostic radiotracers, 99mTc-MIBI and 18FDG. European Journal of Pharmaceutical Sciences, 41, 665–669.PubMedCrossRef
106.
go back to reference Watanabe, T., Naito, M., Kokubu, N., & Tsuruo, T. (1997). Regression of established tumors expressing P-glycoprotein by combinations of adriamycin, cyclosporin derivatives, and MRK-16 antibodies. Journal of the National Cancer Institute, 89, 512–518.PubMedCrossRef Watanabe, T., Naito, M., Kokubu, N., & Tsuruo, T. (1997). Regression of established tumors expressing P-glycoprotein by combinations of adriamycin, cyclosporin derivatives, and MRK-16 antibodies. Journal of the National Cancer Institute, 89, 512–518.PubMedCrossRef
107.
go back to reference Matsuo, H., et al. (2001). Possibility of the reversal of multidrug resistance and the avoidance of side effects by liposomes modified with MRK-16, a monoclonal antibody to P-glycoprotein. Journal of Controlled Release, 77, 77–86.PubMedCrossRef Matsuo, H., et al. (2001). Possibility of the reversal of multidrug resistance and the avoidance of side effects by liposomes modified with MRK-16, a monoclonal antibody to P-glycoprotein. Journal of Controlled Release, 77, 77–86.PubMedCrossRef
108.
go back to reference Gatouillat, G., et al. (2007). Immunization with liposome-anchored pegylated peptides modulates doxorubicin sensitivity in P-glycoprotein-expressing P388 cells. Cancer Letters, 257, 165–171.PubMedCrossRef Gatouillat, G., et al. (2007). Immunization with liposome-anchored pegylated peptides modulates doxorubicin sensitivity in P-glycoprotein-expressing P388 cells. Cancer Letters, 257, 165–171.PubMedCrossRef
109.
go back to reference Madoulet, C., Perrin, L., Tosi, P. F., & Albert, P. (2006). Anti-tumor immunotherapy against multidrug resistance. Annales Pharmaceutiques Françaises, 64, 87–96.PubMedCrossRef Madoulet, C., Perrin, L., Tosi, P. F., & Albert, P. (2006). Anti-tumor immunotherapy against multidrug resistance. Annales Pharmaceutiques Françaises, 64, 87–96.PubMedCrossRef
110.
go back to reference Beck, W. T. (1995). Circumvention of multidrug resistance with anti-P-glycoprotein antibodies: Clinical potential or experimental artifact? Journal of the National Cancer Institute, 87, 73–75.PubMedCrossRef Beck, W. T. (1995). Circumvention of multidrug resistance with anti-P-glycoprotein antibodies: Clinical potential or experimental artifact? Journal of the National Cancer Institute, 87, 73–75.PubMedCrossRef
111.
go back to reference Comerford, K. M., et al. (2002). Hypoxia-inducible factor-1-dependent regulation of the multidrug resistance (MDR1) gene. Cancer Research, 62, 3387–3394.PubMed Comerford, K. M., et al. (2002). Hypoxia-inducible factor-1-dependent regulation of the multidrug resistance (MDR1) gene. Cancer Research, 62, 3387–3394.PubMed
112.
go back to reference Han, Z., et al. (2007). Phospho Akt mediates multidrug resistance of gastric cancer cells through regulation of P-gp, Bcl-2 and Bax. Journal of Experimental & Clinical Cancer Research, 26, 261–268. Han, Z., et al. (2007). Phospho Akt mediates multidrug resistance of gastric cancer cells through regulation of P-gp, Bcl-2 and Bax. Journal of Experimental & Clinical Cancer Research, 26, 261–268.
113.
go back to reference Hu, X. F., Li, J., Yang, E., Vandervalk, S., & Xing, P. X. (2007). Anti-Cripto Mab inhibit tumour growth and overcome MDR in a human leukaemia MDR cell line by inhibition of Akt and activation of JNK/SAPK and bad death pathways. British Journal of Cancer, 96, 918–927.PubMedCrossRef Hu, X. F., Li, J., Yang, E., Vandervalk, S., & Xing, P. X. (2007). Anti-Cripto Mab inhibit tumour growth and overcome MDR in a human leukaemia MDR cell line by inhibition of Akt and activation of JNK/SAPK and bad death pathways. British Journal of Cancer, 96, 918–927.PubMedCrossRef
114.
go back to reference Liu, B., Qu, L., & Tao, H. (2010). Cyclo-oxygenase 2 up-regulates the effect of multidrug resistance. Cell Biology International, 34, 21–25. Liu, B., Qu, L., & Tao, H. (2010). Cyclo-oxygenase 2 up-regulates the effect of multidrug resistance. Cell Biology International, 34, 21–25.
115.
go back to reference Zhang, Y., Laterra, J., & Pomper, M. G. (2009). Hedgehog pathway inhibitor HhAntag691 is a potent inhibitor of ABCG2/BCRP and ABCB1/Pgp. Neoplasia, 11, 96–101.PubMed Zhang, Y., Laterra, J., & Pomper, M. G. (2009). Hedgehog pathway inhibitor HhAntag691 is a potent inhibitor of ABCG2/BCRP and ABCB1/Pgp. Neoplasia, 11, 96–101.PubMed
116.
go back to reference Cui, D., Xu, Q., Wang, K., & Che, X. (2010). Gli1 is a potential target for alleviating multidrug resistance of gliomas. Journal of the Neurological Sciences, 288, 156–166.PubMedCrossRef Cui, D., Xu, Q., Wang, K., & Che, X. (2010). Gli1 is a potential target for alleviating multidrug resistance of gliomas. Journal of the Neurological Sciences, 288, 156–166.PubMedCrossRef
117.
go back to reference Chen, T. (2010). Overcoming drug resistance by regulating nuclear receptors. Advanced Drug Delivery Reviews, 62, 1257–1264.PubMedCrossRef Chen, T. (2010). Overcoming drug resistance by regulating nuclear receptors. Advanced Drug Delivery Reviews, 62, 1257–1264.PubMedCrossRef
118.
go back to reference Chen, Y., Tang, Y., Wang, M. T., Zeng, S., & Nie, D. (2007). Human pregnane X receptor and resistance to chemotherapy in prostate cancer. Cancer Research, 67, 10361–10367.PubMedCrossRef Chen, Y., Tang, Y., Wang, M. T., Zeng, S., & Nie, D. (2007). Human pregnane X receptor and resistance to chemotherapy in prostate cancer. Cancer Research, 67, 10361–10367.PubMedCrossRef
119.
go back to reference Masuyama, H., Nakatsukasa, H., Takamoto, N., & Hiramatsu, Y. (2007). Down-regulation of pregnane X receptor contributes to cell growth inhibition and apoptosis by anticancer agents in endometrial cancer cells. Molecular Pharmacology, 72, 1045–1053.PubMedCrossRef Masuyama, H., Nakatsukasa, H., Takamoto, N., & Hiramatsu, Y. (2007). Down-regulation of pregnane X receptor contributes to cell growth inhibition and apoptosis by anticancer agents in endometrial cancer cells. Molecular Pharmacology, 72, 1045–1053.PubMedCrossRef
120.
go back to reference Stewart, A. J., et al. (1996). Reduction of expression of the multidrug resistance protein (MRP) in human tumor cells by antisense phosphorothioate oligonucleotides. Biochemical Pharmacology, 51, 461–469.PubMedCrossRef Stewart, A. J., et al. (1996). Reduction of expression of the multidrug resistance protein (MRP) in human tumor cells by antisense phosphorothioate oligonucleotides. Biochemical Pharmacology, 51, 461–469.PubMedCrossRef
121.
go back to reference Osada, H., et al. (2003). Reversal of drug resistance mediated by hammerhead ribozyme against multidrug resistance-associated protein 1 in a human glioma cell line. International Journal of Oncology, 22, 823–827.PubMed Osada, H., et al. (2003). Reversal of drug resistance mediated by hammerhead ribozyme against multidrug resistance-associated protein 1 in a human glioma cell line. International Journal of Oncology, 22, 823–827.PubMed
122.
go back to reference Kowalski, P., Farley, K. M., Lage, H., & Schneider, E. (2004). Effective knock down of very high ABCG2 expression by a hammerhead ribozyme. Anticancer Research, 24, 2231–2235.PubMed Kowalski, P., Farley, K. M., Lage, H., & Schneider, E. (2004). Effective knock down of very high ABCG2 expression by a hammerhead ribozyme. Anticancer Research, 24, 2231–2235.PubMed
123.
go back to reference Gao, P., et al. (2007). Reversal of drug resistance in breast carcinoma cells by anti-mdr1 ribozyme regulated by the tumor-specific MUC-1 promoter. Cancer Letters, 256, 81–89.PubMedCrossRef Gao, P., et al. (2007). Reversal of drug resistance in breast carcinoma cells by anti-mdr1 ribozyme regulated by the tumor-specific MUC-1 promoter. Cancer Letters, 256, 81–89.PubMedCrossRef
124.
go back to reference Nadali, F., et al. (2007). Multidrug resistance inhibition by antisense oligonucleotide against MDR1/mRNA in P-glycoprotein expressing leukemic cells. Hematology, 12, 393–401.PubMedCrossRef Nadali, F., et al. (2007). Multidrug resistance inhibition by antisense oligonucleotide against MDR1/mRNA in P-glycoprotein expressing leukemic cells. Hematology, 12, 393–401.PubMedCrossRef
125.
go back to reference Kowalski, P., Surowiak, P., & Lage, H. (2005). Reversal of different drug-resistant phenotypes by an autocatalytic multitarget multiribozyme directed against the transcripts of the ABC transporters MDR1/P-gp, MRP2, and BCRP. Molecular Therapy, 11, 508–522.PubMedCrossRef Kowalski, P., Surowiak, P., & Lage, H. (2005). Reversal of different drug-resistant phenotypes by an autocatalytic multitarget multiribozyme directed against the transcripts of the ABC transporters MDR1/P-gp, MRP2, and BCRP. Molecular Therapy, 11, 508–522.PubMedCrossRef
126.
go back to reference Abbasi M., Lavasanifar A., & Uluda H. (2011). Recent attempts at RNAi-mediated P-glycoprotein downregulation for reversal of multidrug resistance in cancer. Medicinal Research Reviews. doi:10.1002/med.20244. Abbasi M., Lavasanifar A., & Uluda H. (2011). Recent attempts at RNAi-mediated P-glycoprotein downregulation for reversal of multidrug resistance in cancer. Medicinal Research Reviews. doi:10.​1002/​med.​20244.
127.
go back to reference Stege, A., Priebsch, A., Nieth, C., & Lage, H. (2004). Stable and complete overcoming of MDR1/P-glycoprotein-mediated multidrug resistance in human gastric carcinoma cells by RNA interference. Cancer Gene Therapy, 11, 699–706.PubMedCrossRef Stege, A., Priebsch, A., Nieth, C., & Lage, H. (2004). Stable and complete overcoming of MDR1/P-glycoprotein-mediated multidrug resistance in human gastric carcinoma cells by RNA interference. Cancer Gene Therapy, 11, 699–706.PubMedCrossRef
128.
go back to reference Yague, E., Higgins, C. F., & Raguz, S. (2004). Complete reversal of multidrug resistance by stable expression of small interfering RNAs targeting MDR1. Gene Therapy, 11, 1170–1174.PubMedCrossRef Yague, E., Higgins, C. F., & Raguz, S. (2004). Complete reversal of multidrug resistance by stable expression of small interfering RNAs targeting MDR1. Gene Therapy, 11, 1170–1174.PubMedCrossRef
129.
go back to reference Stein, U., et al. (2008). Complete in vivo reversal of the multidrug resistance phenotype by jet-injection of anti-MDR1 short hairpin RNA-encoding plasmid DNA. Molecular Therapy, 16, 178–186.PubMedCrossRef Stein, U., et al. (2008). Complete in vivo reversal of the multidrug resistance phenotype by jet-injection of anti-MDR1 short hairpin RNA-encoding plasmid DNA. Molecular Therapy, 16, 178–186.PubMedCrossRef
130.
go back to reference Pichler, A., Zelcer, N., Prior, J. L., Kuil, A. J., & Piwnica-Worms, D. (2005). In vivo RNA interference-mediated ablation of MDR1 P-glycoprotein. Clinical Cancer Research, 11, 4487–4494.PubMedCrossRef Pichler, A., Zelcer, N., Prior, J. L., Kuil, A. J., & Piwnica-Worms, D. (2005). In vivo RNA interference-mediated ablation of MDR1 P-glycoprotein. Clinical Cancer Research, 11, 4487–4494.PubMedCrossRef
131.
go back to reference Xiao, H., et al. (2008). In vivo reversal of P-glycoprotein-mediated multidrug resistance by efficient delivery of stealth RNAi. Basic & Clinical Pharmacology & Toxicology, 103, 342–348.CrossRef Xiao, H., et al. (2008). In vivo reversal of P-glycoprotein-mediated multidrug resistance by efficient delivery of stealth RNAi. Basic & Clinical Pharmacology & Toxicology, 103, 342–348.CrossRef
132.
go back to reference Patutina, O. A., et al. (2010). The siRNA targeted to mdr1b and mdr1a mRNAs in vivo sensitizes murine lymphosarcoma to chemotherapy. BMC Cancer, 10, 204.PubMedCrossRef Patutina, O. A., et al. (2010). The siRNA targeted to mdr1b and mdr1a mRNAs in vivo sensitizes murine lymphosarcoma to chemotherapy. BMC Cancer, 10, 204.PubMedCrossRef
133.
go back to reference Sioud, M. (2011). Promises and challenges in developing RNAi as a research tool and therapy. Methods in Molecular Biology, 703, 173–187.PubMedCrossRef Sioud, M. (2011). Promises and challenges in developing RNAi as a research tool and therapy. Methods in Molecular Biology, 703, 173–187.PubMedCrossRef
134.
go back to reference Blanco, E., Hsiao, A., Mann, A. P., Landry, M. G., Meric-Bernstam, F., & Ferrari, M. (2011). Nanomedicine in cancer therapy: Innovative trends and prospects. Cancer Science, 102, 1247–1252.PubMedCrossRef Blanco, E., Hsiao, A., Mann, A. P., Landry, M. G., Meric-Bernstam, F., & Ferrari, M. (2011). Nanomedicine in cancer therapy: Innovative trends and prospects. Cancer Science, 102, 1247–1252.PubMedCrossRef
135.
go back to reference Patel, N. R., Rathi, A., Mongayt, D., & Torchilin, V. P. (2011). Reversal of multidrug resistance by co-delivery of tariquidar (XR9576) and paclitaxel using long-circulating liposomes. International Journal of Pharmaceutics, 416, 296–299.PubMedCrossRef Patel, N. R., Rathi, A., Mongayt, D., & Torchilin, V. P. (2011). Reversal of multidrug resistance by co-delivery of tariquidar (XR9576) and paclitaxel using long-circulating liposomes. International Journal of Pharmaceutics, 416, 296–299.PubMedCrossRef
136.
go back to reference Wang, F., et al. (2011). Synergistic effect of folate-mediated targeting and verapamil-mediated P-gp inhibition with paclitaxel-polymer micelles to overcome multi-drug resistance. Biomaterials, 32, 9444–9456.PubMedCrossRef Wang, F., et al. (2011). Synergistic effect of folate-mediated targeting and verapamil-mediated P-gp inhibition with paclitaxel-polymer micelles to overcome multi-drug resistance. Biomaterials, 32, 9444–9456.PubMedCrossRef
137.
go back to reference van Vlerken, L. E., Duan, Z., Little, S. R., Seiden, M. V., & Amiji, M. M. (2008). Biodistribution and pharmacokinetic analysis of paclitaxel and ceramide administered in multifunctional polymer-blend nanoparticles in drug resistant breast cancer model. Molecular Pharmaceutics, 5, 516–526.PubMedCrossRef van Vlerken, L. E., Duan, Z., Little, S. R., Seiden, M. V., & Amiji, M. M. (2008). Biodistribution and pharmacokinetic analysis of paclitaxel and ceramide administered in multifunctional polymer-blend nanoparticles in drug resistant breast cancer model. Molecular Pharmaceutics, 5, 516–526.PubMedCrossRef
138.
go back to reference van Vlerken, L. E., Duan, Z., Little, S. R., Seiden, M. V., & Amiji, M. M. (2010). Augmentation of therapeutic efficacy in drug-resistant tumor models using ceramide coadministration in temporal-controlled polymer-blend nanoparticle delivery systems. The AAPS Journal, 12, 171–180.PubMedCrossRef van Vlerken, L. E., Duan, Z., Little, S. R., Seiden, M. V., & Amiji, M. M. (2010). Augmentation of therapeutic efficacy in drug-resistant tumor models using ceramide coadministration in temporal-controlled polymer-blend nanoparticle delivery systems. The AAPS Journal, 12, 171–180.PubMedCrossRef
139.
go back to reference Meng, H., et al. (2010). Engineered design of mesoporous silica nanoparticles to deliver doxorubicin and P-glycoprotein siRNA to overcome drug resistance in a cancer cell line. ACS Nano, 4, 4539–4550.PubMedCrossRef Meng, H., et al. (2010). Engineered design of mesoporous silica nanoparticles to deliver doxorubicin and P-glycoprotein siRNA to overcome drug resistance in a cancer cell line. ACS Nano, 4, 4539–4550.PubMedCrossRef
140.
go back to reference Lhomme, C., et al. (2008). Phase III study of valspodar (PSC 833) combined with paclitaxel and carboplatin compared with paclitaxel and carboplatin alone in patients with stage IV or suboptimally debulked stage III epithelial ovarian cancer or primary peritoneal cancer. Journal of Clinical Oncology, 26, 2674–2682.PubMedCrossRef Lhomme, C., et al. (2008). Phase III study of valspodar (PSC 833) combined with paclitaxel and carboplatin compared with paclitaxel and carboplatin alone in patients with stage IV or suboptimally debulked stage III epithelial ovarian cancer or primary peritoneal cancer. Journal of Clinical Oncology, 26, 2674–2682.PubMedCrossRef
141.
go back to reference Friedenberg, W. R., et al. (2006). Phase III study of PSC-833 (valspodar) in combination with vincristine, doxorubicin, and dexamethasone (valspodar/VAD) versus VAD alone in patients with recurring or refractory multiple myeloma (E1A95): A trial of the Eastern Cooperative Oncology Group. Cancer, 106, 830–838.PubMedCrossRef Friedenberg, W. R., et al. (2006). Phase III study of PSC-833 (valspodar) in combination with vincristine, doxorubicin, and dexamethasone (valspodar/VAD) versus VAD alone in patients with recurring or refractory multiple myeloma (E1A95): A trial of the Eastern Cooperative Oncology Group. Cancer, 106, 830–838.PubMedCrossRef
142.
go back to reference Greenberg, P. L., et al. (2004). Mitoxantrone, etoposide, and cytarabine with or without valspodar in patients with relapsed or refractory acute myeloid leukemia and high-risk myelodysplastic syndrome: A phase III trial (E2995). Journal of Clinical Oncology, 22, 1078–1086.PubMedCrossRef Greenberg, P. L., et al. (2004). Mitoxantrone, etoposide, and cytarabine with or without valspodar in patients with relapsed or refractory acute myeloid leukemia and high-risk myelodysplastic syndrome: A phase III trial (E2995). Journal of Clinical Oncology, 22, 1078–1086.PubMedCrossRef
143.
go back to reference Khdair, A., et al. (2010). Nanoparticle-mediated combination chemotherapy and photodynamic therapy overcomes tumor drug resistance. Journal of Controlled Release, 141, 137–144.PubMedCrossRef Khdair, A., et al. (2010). Nanoparticle-mediated combination chemotherapy and photodynamic therapy overcomes tumor drug resistance. Journal of Controlled Release, 141, 137–144.PubMedCrossRef
144.
go back to reference Huang, I. P., et al. (2011). Enhanced chemotherapy of cancer using pH-sensitive mesoporous silica nanoparticles to antagonize P-glycoprotein-mediated drug resistance. Molecular Cancer Therapeutics, 10, 761–769.PubMedCrossRef Huang, I. P., et al. (2011). Enhanced chemotherapy of cancer using pH-sensitive mesoporous silica nanoparticles to antagonize P-glycoprotein-mediated drug resistance. Molecular Cancer Therapeutics, 10, 761–769.PubMedCrossRef
145.
go back to reference Chen, B., et al. (2009). Reversal of multidrug resistance by magnetic Fe3O4 nanoparticle copolymerizating daunorubicin and 5-bromotetrandrine in xenograft nude-mice. International Journal of Nanomedicine, 4, 73–78.PubMedCrossRef Chen, B., et al. (2009). Reversal of multidrug resistance by magnetic Fe3O4 nanoparticle copolymerizating daunorubicin and 5-bromotetrandrine in xenograft nude-mice. International Journal of Nanomedicine, 4, 73–78.PubMedCrossRef
146.
go back to reference Chen, B. A., et al. (2009). Daunorubicin-loaded magnetic nanoparticles of Fe3O4 overcome multidrug resistance and induce apoptosis of K562-n/VCR cells in vivo. International Journal of Nanomedicine, 4, 201–208.PubMedCrossRef Chen, B. A., et al. (2009). Daunorubicin-loaded magnetic nanoparticles of Fe3O4 overcome multidrug resistance and induce apoptosis of K562-n/VCR cells in vivo. International Journal of Nanomedicine, 4, 201–208.PubMedCrossRef
147.
go back to reference Ganta, S., Devalapally, H., & Amiji, M. (2010). Curcumin enhances oral bioavailability and anti-tumor therapeutic efficacy of paclitaxel upon administration in nanoemulsion formulation. Journal of Pharmaceutical Sciences, 99, 4630–4641.PubMedCrossRef Ganta, S., Devalapally, H., & Amiji, M. (2010). Curcumin enhances oral bioavailability and anti-tumor therapeutic efficacy of paclitaxel upon administration in nanoemulsion formulation. Journal of Pharmaceutical Sciences, 99, 4630–4641.PubMedCrossRef
148.
go back to reference Wang, X., et al. (2011). A folate receptor-targeting nanoparticle minimizes drug resistance in a human cancer model. ACS Nano, 5, 6184–6194.PubMedCrossRef Wang, X., et al. (2011). A folate receptor-targeting nanoparticle minimizes drug resistance in a human cancer model. ACS Nano, 5, 6184–6194.PubMedCrossRef
149.
go back to reference Wang, X., et al. (2009). HFT-T, a targeting nanoparticle, enhances specific delivery of paclitaxel to folate receptor-positive tumors. ACS Nano, 3, 3165–3174.PubMedCrossRef Wang, X., et al. (2009). HFT-T, a targeting nanoparticle, enhances specific delivery of paclitaxel to folate receptor-positive tumors. ACS Nano, 3, 3165–3174.PubMedCrossRef
150.
go back to reference Dong, X., et al. (2009). Doxorubicin and paclitaxel-loaded lipid-based nanoparticles overcome multidrug resistance by inhibiting P-glycoprotein and depleting ATP. Cancer Research, 69, 3918–3926.PubMedCrossRef Dong, X., et al. (2009). Doxorubicin and paclitaxel-loaded lipid-based nanoparticles overcome multidrug resistance by inhibiting P-glycoprotein and depleting ATP. Cancer Research, 69, 3918–3926.PubMedCrossRef
151.
go back to reference Patil, Y., Sadhukha, T., Ma, L., & Panyam, J. (2009). Nanoparticle-mediated simultaneous and targeted delivery of paclitaxel and tariquidar overcomes tumor drug resistance. Journal of Controlled Release, 136, 21–29.PubMedCrossRef Patil, Y., Sadhukha, T., Ma, L., & Panyam, J. (2009). Nanoparticle-mediated simultaneous and targeted delivery of paclitaxel and tariquidar overcomes tumor drug resistance. Journal of Controlled Release, 136, 21–29.PubMedCrossRef
152.
go back to reference Patil, Y. B., Swaminathan, S. K., Sadhukha, T., Ma, L., & Panyam, J. (2010). The use of nanoparticle-mediated targeted gene silencing and drug delivery to overcome tumor drug resistance. Biomaterials, 31, 358–365.PubMedCrossRef Patil, Y. B., Swaminathan, S. K., Sadhukha, T., Ma, L., & Panyam, J. (2010). The use of nanoparticle-mediated targeted gene silencing and drug delivery to overcome tumor drug resistance. Biomaterials, 31, 358–365.PubMedCrossRef
Metadata
Title
Reversal of ATP-binding cassette drug transporter activity to modulate chemoresistance: why has it failed to provide clinical benefit?
Authors
Man Yu
Alberto Ocana
Ian F. Tannock
Publication date
01-06-2013
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 1-2/2013
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-012-9402-8

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