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Published in: Breast Cancer Research and Treatment 2/2008

01-01-2008 | Preclinical Study

Diminished feedback regulation of proteasome expression and resistance to proteasome inhibitors in breast cancer cells

Authors: Haiming Xu, Donghong Ju, Tiffany Jarois, Youming Xie

Published in: Breast Cancer Research and Treatment | Issue 2/2008

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Abstract

Clinical trials with proteasome inhibitor Bortezomib (also named Velcade or PS-341) has shown promising results for some cancers. However, other types of cancers including breast cancer do not respond well to Bortezomib. To understand the cause of the drug resistance, we compared the regulation of proteasome expression and the sensitivity to proteasome inhibitors between human breast cancer cells and nontumorigenic mammary epithelial cells. We found that, while the endogenous expression level is much higher, the potential of feedback expression in response to proteasome inhibitors is much lower in the breast cancer cells. Furthermore, the breast cancer cells are much more resistant to proteasome inhibitors compared to the nontumorigenic mammary epithelial cells. Biochemical analysis showed that the pathway of Bortezomib-induced apoptosis is apparently defective in the breast cancer cells. Together, these results provide an explanation for the inefficacy of Bortezomib in the clinical trials for breast cancer patients. The likelihood of combination therapy with Bortezomib and other anti-cancer agents for breast cancer is also discussed.
Literature
1.
go back to reference Hershko A, Ciechanover A, Varshavsky A (2000) The ubiquitin system. Nature Med 10:1073–1081CrossRef Hershko A, Ciechanover A, Varshavsky A (2000) The ubiquitin system. Nature Med 10:1073–1081CrossRef
2.
go back to reference Schwartz AL, Ciechanover A (1999) The ubiquitin-proteasome pathway and pathogenesis of human diseases. Annu Rev Med 50:57–74PubMedCrossRef Schwartz AL, Ciechanover A (1999) The ubiquitin-proteasome pathway and pathogenesis of human diseases. Annu Rev Med 50:57–74PubMedCrossRef
3.
go back to reference Teicher BA, Ara G, Herbst R, Palombella VJ, Adams J (1999) The proteasome inhibitor PS-341 in cancer therapy. Clin Cancer Res 5:2638–2645PubMed Teicher BA, Ara G, Herbst R, Palombella VJ, Adams J (1999) The proteasome inhibitor PS-341 in cancer therapy. Clin Cancer Res 5:2638–2645PubMed
4.
go back to reference Banerjee D, Liefshitz A (2001) Potential of the proteasomal inhibitor MG-132 as an anticancer agent, alone and in combination. Anticancer Res 21:3941–3947PubMed Banerjee D, Liefshitz A (2001) Potential of the proteasomal inhibitor MG-132 as an anticancer agent, alone and in combination. Anticancer Res 21:3941–3947PubMed
5.
go back to reference Shah SA, Potter MW, McDade TP, et al (2001) 26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer. J Cell Biochem 82:110–122PubMedCrossRef Shah SA, Potter MW, McDade TP, et al (2001) 26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer. J Cell Biochem 82:110–122PubMedCrossRef
6.
go back to reference Goy A, Younes A, McLaughlin P, et al (2005) Phase II study of proteasome inhibitor bortezomib in relapsed or refractory B-cell non-Hodgkin’s lymphoma. J Clin Oncol 23:667–675PubMedCrossRef Goy A, Younes A, McLaughlin P, et al (2005) Phase II study of proteasome inhibitor bortezomib in relapsed or refractory B-cell non-Hodgkin’s lymphoma. J Clin Oncol 23:667–675PubMedCrossRef
7.
go back to reference Pahler JC, Ruiz S, Niemer I, et al (2003) Effects of the proteasome inhibitor, bortezomib, on apoptosis in isolated lymphocytes obtained from patients with chronic lymphocytic leukemia. Clin Cancer Res 9:4570–4577PubMed Pahler JC, Ruiz S, Niemer I, et al (2003) Effects of the proteasome inhibitor, bortezomib, on apoptosis in isolated lymphocytes obtained from patients with chronic lymphocytic leukemia. Clin Cancer Res 9:4570–4577PubMed
8.
go back to reference Orlowski RZ, Voorhees PM, Garcia RA, et al (2005) Phase 1 trial of the proteasome inhibitor bortezomib and pegylated liposomal doxorubicin in patients with advanced hematologic malignancies. Blood 105:3058–3065PubMedCrossRef Orlowski RZ, Voorhees PM, Garcia RA, et al (2005) Phase 1 trial of the proteasome inhibitor bortezomib and pegylated liposomal doxorubicin in patients with advanced hematologic malignancies. Blood 105:3058–3065PubMedCrossRef
9.
go back to reference Yang CH, Gonzalez-Angulo AM, Reuben JM, et al (2006). Bortezomib (VELCADE(R)) in metastatic breast cancer: pharmacodynamics, biological effects, and prediction of clinical benefits. Ann Oncol 17:813–817PubMedCrossRef Yang CH, Gonzalez-Angulo AM, Reuben JM, et al (2006). Bortezomib (VELCADE(R)) in metastatic breast cancer: pharmacodynamics, biological effects, and prediction of clinical benefits. Ann Oncol 17:813–817PubMedCrossRef
10.
go back to reference Markovic SN, Geyer SM, Dawkins F, et al (2005) A phase II study of bortezomib in the treatment of metastatic malignant melanoma. Cancer 103:2584–2589PubMedCrossRef Markovic SN, Geyer SM, Dawkins F, et al (2005) A phase II study of bortezomib in the treatment of metastatic malignant melanoma. Cancer 103:2584–2589PubMedCrossRef
11.
go back to reference Mackay H, Hedley D, Major P, et al (2005) A phase II trial with pharmacodynamic endpoints of the proteasome inhibitor bortezomib in patients with metastatic colorectal cancer. Clin Cancer Res 11:5526–5533PubMedCrossRef Mackay H, Hedley D, Major P, et al (2005) A phase II trial with pharmacodynamic endpoints of the proteasome inhibitor bortezomib in patients with metastatic colorectal cancer. Clin Cancer Res 11:5526–5533PubMedCrossRef
12.
go back to reference Maki RG, Kraft AS, Scheu K, et al (2005) A multicenter Phase II study of bortezomib in recurrent or metastatic sarcomas. Cancer 103:1431–1438PubMedCrossRef Maki RG, Kraft AS, Scheu K, et al (2005) A multicenter Phase II study of bortezomib in recurrent or metastatic sarcomas. Cancer 103:1431–1438PubMedCrossRef
13.
go back to reference Shah MH, Young D, Kindler HL, et al (2004) Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors. Clin Cancer Res 10:6111–6118PubMedCrossRef Shah MH, Young D, Kindler HL, et al (2004) Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors. Clin Cancer Res 10:6111–6118PubMedCrossRef
14.
go back to reference Xie Y, Varshavsky A (2001) RPN4 is a ligand, substrate, and transcriptional regulator of the 26S proteasome: a negative feedback circuit. Proc Natl Acad Sci USA 98:3056–3061PubMedCrossRef Xie Y, Varshavsky A (2001) RPN4 is a ligand, substrate, and transcriptional regulator of the 26S proteasome: a negative feedback circuit. Proc Natl Acad Sci USA 98:3056–3061PubMedCrossRef
15.
go back to reference Ju D, Wang L, Mao X, Xie Y (2004) Homeostatic regulation of the proteasome via an Rpn4-dependent feedback circuit. Biochem Biophys Res Commun 321:51–57PubMedCrossRef Ju D, Wang L, Mao X, Xie Y (2004) Homeostatic regulation of the proteasome via an Rpn4-dependent feedback circuit. Biochem Biophys Res Commun 321:51–57PubMedCrossRef
16.
go back to reference Fleming JA, Lightcap ES, Sadis S, Thoroddsen V, Bulawa CE, Blackman RK (2002) Complementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341. Proc Natl Acad Sci USA 99:1461–1466PubMedCrossRef Fleming JA, Lightcap ES, Sadis S, Thoroddsen V, Bulawa CE, Blackman RK (2002) Complementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341. Proc Natl Acad Sci USA 99:1461–1466PubMedCrossRef
17.
go back to reference Meiners S, Heyken D, Weller A, et al (2003) Inhibition of proteasome activity induces concerted expression of proteasome genes and de novo formation of Mammalian proteasomes. J Biol Chem 278:21517–21525PubMedCrossRef Meiners S, Heyken D, Weller A, et al (2003) Inhibition of proteasome activity induces concerted expression of proteasome genes and de novo formation of Mammalian proteasomes. J Biol Chem 278:21517–21525PubMedCrossRef
18.
go back to reference Lee CS, Tee LY, Warmke T, et al (2004) A proteasomal stress response: pre-treatment with proteasome inhibitors increases proteasome activity and reduces neuronal vulnerability to oxidative injury. J Neurochem 91:996–1006PubMedCrossRef Lee CS, Tee LY, Warmke T, et al (2004) A proteasomal stress response: pre-treatment with proteasome inhibitors increases proteasome activity and reduces neuronal vulnerability to oxidative injury. J Neurochem 91:996–1006PubMedCrossRef
19.
go back to reference Lundgren J, Masson P, Realini CA, Young P (2003) Use of RNA interference and complementation to study the function of the Drosophila and human 26S proteasome subunit S13. Mol Cell Biol 23:5320–5330PubMedCrossRef Lundgren J, Masson P, Realini CA, Young P (2003) Use of RNA interference and complementation to study the function of the Drosophila and human 26S proteasome subunit S13. Mol Cell Biol 23:5320–5330PubMedCrossRef
20.
go back to reference Wójcik C, DeMartino GN (2002) RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/proteasome-dependent proteolysis. J Biol Chem 277:6188–6197PubMedCrossRef Wójcik C, DeMartino GN (2002) RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/proteasome-dependent proteolysis. J Biol Chem 277:6188–6197PubMedCrossRef
21.
go back to reference Ding Q, Dimayuga E, Markesbery WR, Keller JN (2006) Proteasome inhibition induces reversible impairments in protein synthesis. FASEB J 20:1055–1063PubMedCrossRef Ding Q, Dimayuga E, Markesbery WR, Keller JN (2006) Proteasome inhibition induces reversible impairments in protein synthesis. FASEB J 20:1055–1063PubMedCrossRef
22.
go back to reference Dawson PJ, Wolman SR, Tait L, Heppner GH, Miller FR (1996) MCF10AT: a model for the evolution of cancer from proliferative breast disease. Am J Pathol 148:313–319PubMed Dawson PJ, Wolman SR, Tait L, Heppner GH, Miller FR (1996) MCF10AT: a model for the evolution of cancer from proliferative breast disease. Am J Pathol 148:313–319PubMed
23.
go back to reference Chen L, Madura K (2005) Increased proteasome activity, ubiquitin-conjugating enzymes, and eEF1A translation factor detected in breast cancer tissue. Cancer Res 65:5599–5606PubMedCrossRef Chen L, Madura K (2005) Increased proteasome activity, ubiquitin-conjugating enzymes, and eEF1A translation factor detected in breast cancer tissue. Cancer Res 65:5599–5606PubMedCrossRef
24.
go back to reference Kumatori A, Tanaka K, Inamura N, et al (1990) Abnormally high expression of proteasomes in human leukemic cells. Proc Natl Acad Sci USA 87:7071–7075PubMedCrossRef Kumatori A, Tanaka K, Inamura N, et al (1990) Abnormally high expression of proteasomes in human leukemic cells. Proc Natl Acad Sci USA 87:7071–7075PubMedCrossRef
25.
go back to reference Cortes J, Thomas D, Koller C, et al (2004) Phase I study of bortezomib in refractory or relapsed acute leukemias. Clin Cancer Res 10:3371–3376PubMedCrossRef Cortes J, Thomas D, Koller C, et al (2004) Phase I study of bortezomib in refractory or relapsed acute leukemias. Clin Cancer Res 10:3371–3376PubMedCrossRef
26.
go back to reference Yu J, Tiwari S, Steiner P, Zhang L (2003) Differential apoptotic response to the proteasome inhibitor Bortezomib [VELCADE, PS-341] in Bax-deficient and p21-deficient colon cancer cells. Cancer Biol Ther 2:694–699PubMed Yu J, Tiwari S, Steiner P, Zhang L (2003) Differential apoptotic response to the proteasome inhibitor Bortezomib [VELCADE, PS-341] in Bax-deficient and p21-deficient colon cancer cells. Cancer Biol Ther 2:694–699PubMed
27.
go back to reference Klostergaard J, Leroux ME, Auzenne E, et al (2006) Hyperthermia engages the intrinsic apoptotic pathway by enhancing upstream caspase activation to overcome apoptotic resistance in MCF-7 breast adenocarcinoma cells. J Cell Biochem 98: 356–369PubMedCrossRef Klostergaard J, Leroux ME, Auzenne E, et al (2006) Hyperthermia engages the intrinsic apoptotic pathway by enhancing upstream caspase activation to overcome apoptotic resistance in MCF-7 breast adenocarcinoma cells. J Cell Biochem 98: 356–369PubMedCrossRef
28.
go back to reference Wallner KE, Banda M, Li GC (1987) Hyperthermic enhancement of cell killing by mitomycin C in mitomycin C-resistant Chinese hamster ovary cells. Cancer Res 47:1308–1312PubMed Wallner KE, Banda M, Li GC (1987) Hyperthermic enhancement of cell killing by mitomycin C in mitomycin C-resistant Chinese hamster ovary cells. Cancer Res 47:1308–1312PubMed
29.
go back to reference Ciocca DR, Fuqua SA, Lock-Lim S, Toft DO, Welch WJ, McGuire WL (1992) Response of human breast cancer cells to heat shock and chemotherapeutic drugs. Cancer Res 52:3648–3654PubMed Ciocca DR, Fuqua SA, Lock-Lim S, Toft DO, Welch WJ, McGuire WL (1992) Response of human breast cancer cells to heat shock and chemotherapeutic drugs. Cancer Res 52:3648–3654PubMed
30.
go back to reference Reedijk J (2003) New clues for platinum antitumor chemistry: kinetically controlled metal binding to DNA. Proc Natl Acad Sci USA 100:3611–3616PubMedCrossRef Reedijk J (2003) New clues for platinum antitumor chemistry: kinetically controlled metal binding to DNA. Proc Natl Acad Sci USA 100:3611–3616PubMedCrossRef
31.
go back to reference Nawrocki ST, Carew JS, Pino MS, et al (2005) Bortezomib sensitizes pancreatic cancer cells to endoplasmic reticulum stress-mediated apoptosis. Cancer Res 65:11658–11666PubMedCrossRef Nawrocki ST, Carew JS, Pino MS, et al (2005) Bortezomib sensitizes pancreatic cancer cells to endoplasmic reticulum stress-mediated apoptosis. Cancer Res 65:11658–11666PubMedCrossRef
32.
go back to reference Fribley AM, Evenchik B, Zeng Q, et al (2006) Proteasome inhibitor PS-341 induces apoptosis in cisplatin-resistant squamous cell carcinoma cells by induction of Noxa. J Biol Chem 281:31440–31447PubMedCrossRef Fribley AM, Evenchik B, Zeng Q, et al (2006) Proteasome inhibitor PS-341 induces apoptosis in cisplatin-resistant squamous cell carcinoma cells by induction of Noxa. J Biol Chem 281:31440–31447PubMedCrossRef
33.
go back to reference Zou W, Yue P, Lin N, et al (2006) Vitamin C inactivates the proteasome inhibitor PS-341 in human cancer cells. Clin Cancer Res 12:273–280PubMedCrossRef Zou W, Yue P, Lin N, et al (2006) Vitamin C inactivates the proteasome inhibitor PS-341 in human cancer cells. Clin Cancer Res 12:273–280PubMedCrossRef
Metadata
Title
Diminished feedback regulation of proteasome expression and resistance to proteasome inhibitors in breast cancer cells
Authors
Haiming Xu
Donghong Ju
Tiffany Jarois
Youming Xie
Publication date
01-01-2008
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 2/2008
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-007-9553-4

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