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Published in: Cancer Chemotherapy and Pharmacology 1/2016

01-01-2016 | Original Article

Impact of dexrazoxane on doxorubicin-induced aneuploidy in somatic and germinal cells of male mice

Authors: S. M. Attia, S. F. Ahmad, S. A. Bakheet

Published in: Cancer Chemotherapy and Pharmacology | Issue 1/2016

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Abstract

Purpose

Despite dexrazoxane’s increasing use in mitigating doxorubicin-induced cardiotoxicity, no data are available in the literature on the potential aneugenicity of drug combination. Therefore, detailed evaluation of aneugenic potential of this combination is essential to provide more insights into aneuploidy induction that may play a role in the development of secondary malignancies and reproductive toxicity after treatment with doxorubicin. Thus, our aim was to determine whether dexrazoxane has influence on the aneuploidy induced by doxorubicin in germinal and somatic cells of male mice.

Methods

Sperm BrdU-incorporation assay, sperm FISH assay and the bone marrow micronucleus test complemented by FISH assay were used to determine aneuoploidy. Moreover, the formation of 8-OHdG, one of the oxidative DNA damage by-products, has been evaluated.

Results

Dexrazoxane was not aneugenic at the doses tested. Pre-treatment of mice with dexrazoxane significantly reduced doxorubicin-induced aneuploidy in a dose-dependent manner. Doxorubicin induced marked biochemical alterations characteristic of oxidative DNA damage, and prior administration of dexrazoxane before doxorubicin challenge ameliorated this biochemical marker.

Conclusion

This study provides evidence that dexrazoxane has a protective role in the abatement of doxorubicin-induced aneuploidy. This activity resides, at least in part, in its radical scavenger activity. Thus, dexrazoxane can avert secondary malignancies and abnormal reproductive outcomes in cured cancer patients exposed to doxorubicin.
Literature
1.
go back to reference Hortobagyi GN (1997) Anthracyclines in the treatment of cancer. An overview. Drugs 54(Suppl 4):1–7PubMedCrossRef Hortobagyi GN (1997) Anthracyclines in the treatment of cancer. An overview. Drugs 54(Suppl 4):1–7PubMedCrossRef
2.
go back to reference Gewirtz DA (1999) A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin. Biochem Pharmacol 57(7):727–741PubMedCrossRef Gewirtz DA (1999) A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin. Biochem Pharmacol 57(7):727–741PubMedCrossRef
3.
go back to reference Pai VB, Nahata MC (2000) Cardiotoxicity of chemotherapeutic agents: incidence, treatment and prevention. Drug Saf 22(4):263–302PubMedCrossRef Pai VB, Nahata MC (2000) Cardiotoxicity of chemotherapeutic agents: incidence, treatment and prevention. Drug Saf 22(4):263–302PubMedCrossRef
5.
go back to reference Ganapathi R, Hoeltge G, Casey G, Grabowski D, Neelon R, Ford J (1996) Acquisition of doxorubicin resistance in human leukemia HL-60 cells is reproducibly associated with 7q21 chromosomal anomalies. Cancer Genet Cytogenet 86(2):116–119PubMedCrossRef Ganapathi R, Hoeltge G, Casey G, Grabowski D, Neelon R, Ford J (1996) Acquisition of doxorubicin resistance in human leukemia HL-60 cells is reproducibly associated with 7q21 chromosomal anomalies. Cancer Genet Cytogenet 86(2):116–119PubMedCrossRef
6.
go back to reference Aly MS, Othman OE, El Nahas SM (1999) Specific numerical chromosomal aberrations induced by adriamycin. Environ Mol Mutagen 33(2):161–166PubMedCrossRef Aly MS, Othman OE, El Nahas SM (1999) Specific numerical chromosomal aberrations induced by adriamycin. Environ Mol Mutagen 33(2):161–166PubMedCrossRef
7.
go back to reference Theodore C, Bayle C, Bernheim A, Wibault P (2002) Secondary leukaemia after treating advanced bladder cancer with methotrexate, vinblastine, doxorubicin and cisplatin chemotherapy and radiotherapy. BJU Int 90(4):470–471PubMedCrossRef Theodore C, Bayle C, Bernheim A, Wibault P (2002) Secondary leukaemia after treating advanced bladder cancer with methotrexate, vinblastine, doxorubicin and cisplatin chemotherapy and radiotherapy. BJU Int 90(4):470–471PubMedCrossRef
8.
go back to reference Attia SM (2008) Mutagenicity of some topoisomerase II-interactive agents. Saudi Pharm J 16:1–24 Attia SM (2008) Mutagenicity of some topoisomerase II-interactive agents. Saudi Pharm J 16:1–24
10.
go back to reference Buss JL, Hasinoff BB (1993) The one-ring open hydrolysis product intermediates of the cardioprotective agent ICRF-187 (dexrazoxane) displace iron from iron-anthracycline complexes. Agents Actions 40(1–2):86–95PubMedCrossRef Buss JL, Hasinoff BB (1993) The one-ring open hydrolysis product intermediates of the cardioprotective agent ICRF-187 (dexrazoxane) displace iron from iron-anthracycline complexes. Agents Actions 40(1–2):86–95PubMedCrossRef
12.
go back to reference Pearlman M, Jendiroba D, Pagliaro L, Keyhani A, Liu B, Freireich EJ (2003) Dexrazoxane in combination with anthracyclines lead to a synergistic cytotoxic response in acute myelogenous leukemia cell lines. Leuk Res 27(7):617–626PubMedCrossRef Pearlman M, Jendiroba D, Pagliaro L, Keyhani A, Liu B, Freireich EJ (2003) Dexrazoxane in combination with anthracyclines lead to a synergistic cytotoxic response in acute myelogenous leukemia cell lines. Leuk Res 27(7):617–626PubMedCrossRef
14.
go back to reference Herman EH, Hasinoff BB, Zhang J, Raley LG, Zhang TM, Fukuda Y, Ferrans VJ (1995) Morphologic and morphometric evaluation of the effect of ICRF-187 on bleomycin-induced pulmonary toxicity. Toxicology 98(1–3):163–175PubMedCrossRef Herman EH, Hasinoff BB, Zhang J, Raley LG, Zhang TM, Fukuda Y, Ferrans VJ (1995) Morphologic and morphometric evaluation of the effect of ICRF-187 on bleomycin-induced pulmonary toxicity. Toxicology 98(1–3):163–175PubMedCrossRef
15.
go back to reference Hasinoff BB, Kala SV (1993) The removal of metal ions from transferrin, ferritin and ceruloplasmin by the cardioprotective agent ICRF-187 [(+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane] and its hydrolysis product ADR-925. Agents Actions 39(1–2):72–81PubMedCrossRef Hasinoff BB, Kala SV (1993) The removal of metal ions from transferrin, ferritin and ceruloplasmin by the cardioprotective agent ICRF-187 [(+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane] and its hydrolysis product ADR-925. Agents Actions 39(1–2):72–81PubMedCrossRef
16.
go back to reference Hasinoff BB, Kuschak TI, Yalowich JC, Creighton AM (1995) A QSAR study comparing the cytotoxicity and DNA topoisomerase II inhibitory effects of bisdioxopiperazine analogs of ICRF-187 (dexrazoxane). Biochem Pharmacol 50(7):953–958PubMedCrossRef Hasinoff BB, Kuschak TI, Yalowich JC, Creighton AM (1995) A QSAR study comparing the cytotoxicity and DNA topoisomerase II inhibitory effects of bisdioxopiperazine analogs of ICRF-187 (dexrazoxane). Biochem Pharmacol 50(7):953–958PubMedCrossRef
19.
go back to reference Bakheet SA, Attia SM, Al-Rasheed NM, Al-Harbi MM, Ashour AE, Korashy HM, Abd-Allah AR, Saquib Q, Al-Khedhairy AA, Musarrat J (2011) Salubrious effects of dexrazoxane against teniposide-induced DNA damage and programmed cell death in murine marrow cells. Mutagenesis 26(4):533–543. doi:10.1093/mutage/ger013 PubMedCrossRef Bakheet SA, Attia SM, Al-Rasheed NM, Al-Harbi MM, Ashour AE, Korashy HM, Abd-Allah AR, Saquib Q, Al-Khedhairy AA, Musarrat J (2011) Salubrious effects of dexrazoxane against teniposide-induced DNA damage and programmed cell death in murine marrow cells. Mutagenesis 26(4):533–543. doi:10.​1093/​mutage/​ger013 PubMedCrossRef
20.
21.
go back to reference Schmid TE, Attia S, Baumgartner A, Nuesse M, Adler ID (2001) Effect of chemicals on the duration of male meiosis in mice detected with laser scanning cytometry. Mutagenesis 16(4):339–343PubMedCrossRef Schmid TE, Attia S, Baumgartner A, Nuesse M, Adler ID (2001) Effect of chemicals on the duration of male meiosis in mice detected with laser scanning cytometry. Mutagenesis 16(4):339–343PubMedCrossRef
22.
go back to reference Attia SM, Schmid TE, Badary OA, Hamada FM, Adler ID (2002) Molecular cytogenetic analysis in mouse sperm of chemically induced aneuploidy: studies with topoisomerase II inhibitors. Mutat Res 520(1–2):1–13PubMedCrossRef Attia SM, Schmid TE, Badary OA, Hamada FM, Adler ID (2002) Molecular cytogenetic analysis in mouse sperm of chemically induced aneuploidy: studies with topoisomerase II inhibitors. Mutat Res 520(1–2):1–13PubMedCrossRef
23.
go back to reference Krishna G, Hayashi M (2000) In vivo rodent micronucleus assay: protocol, conduct and data interpretation. Mutat Res 455(1–2):155–166PubMedCrossRef Krishna G, Hayashi M (2000) In vivo rodent micronucleus assay: protocol, conduct and data interpretation. Mutat Res 455(1–2):155–166PubMedCrossRef
24.
go back to reference Attia SM (2009) Use of centromeric and telomeric DNA probes in in situ hybridization for differentiation of micronuclei induced by lomefloxacin. Environ Mol Mutagen 50(5):394–403. doi:10.1002/em.20451 PubMedCrossRef Attia SM (2009) Use of centromeric and telomeric DNA probes in in situ hybridization for differentiation of micronuclei induced by lomefloxacin. Environ Mol Mutagen 50(5):394–403. doi:10.​1002/​em.​20451 PubMedCrossRef
26.
go back to reference Attia SM, Kliesch U, Schriever-Schwemmer G, Badary OA, Hamada FM, Adler ID (2003) Etoposide and merbarone are clastogenic and aneugenic in the mouse bone marrow micronucleus test complemented by fluorescence in situ hybridization with the mouse minor satellite DNA probe. Environ Mol Mutagen 41(2):99–103. doi:10.1002/em.10135 PubMedCrossRef Attia SM, Kliesch U, Schriever-Schwemmer G, Badary OA, Hamada FM, Adler ID (2003) Etoposide and merbarone are clastogenic and aneugenic in the mouse bone marrow micronucleus test complemented by fluorescence in situ hybridization with the mouse minor satellite DNA probe. Environ Mol Mutagen 41(2):99–103. doi:10.​1002/​em.​10135 PubMedCrossRef
28.
go back to reference Ling YH, El-Naggar AK, Priebe W, Perez-Soler R (1996) Cell cycle-dependent cytotoxicity, G2/M phase arrest, and disruption of p34cdc2/cyclin B1 activity induced by doxorubicin in synchronized P388 cells. Mol Pharmacol 49(5):832–841PubMed Ling YH, El-Naggar AK, Priebe W, Perez-Soler R (1996) Cell cycle-dependent cytotoxicity, G2/M phase arrest, and disruption of p34cdc2/cyclin B1 activity induced by doxorubicin in synchronized P388 cells. Mol Pharmacol 49(5):832–841PubMed
30.
go back to reference Adler ID (1993) Synopsis of the in vivo results obtained with the 10 known or suspected aneugens tested in the CEC collaborative study. Mutat Res 287(1):131–137PubMedCrossRef Adler ID (1993) Synopsis of the in vivo results obtained with the 10 known or suspected aneugens tested in the CEC collaborative study. Mutat Res 287(1):131–137PubMedCrossRef
31.
go back to reference Pytel D, Wysocki T, Majsterek I (2006) Comparative study of DNA damage, cell cycle and apoptosis in human K562 and CCRF-CEM leukemia cells: role of BCR/ABL in therapeutic resistance. Comp Biochem Physiol Toxicol Pharmacol CBP 144(1):85–92. doi:10.1016/j.cbpc.2006.06.010 CrossRef Pytel D, Wysocki T, Majsterek I (2006) Comparative study of DNA damage, cell cycle and apoptosis in human K562 and CCRF-CEM leukemia cells: role of BCR/ABL in therapeutic resistance. Comp Biochem Physiol Toxicol Pharmacol CBP 144(1):85–92. doi:10.​1016/​j.​cbpc.​2006.​06.​010 CrossRef
32.
go back to reference Martin RH, Rademaker AW, Leonard NJ (1995) Analysis of chromosomal abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH). Cancer Genet Cytogenet 80(1):29–32PubMedCrossRef Martin RH, Rademaker AW, Leonard NJ (1995) Analysis of chromosomal abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH). Cancer Genet Cytogenet 80(1):29–32PubMedCrossRef
33.
go back to reference Dhawan A, Kayani MA, Parry JM, Parry E, Anderson D (2003) Aneugenic and clastogenic effects of doxorubicin in human lymphocytes. Mutagenesis 18(6):487–490PubMedCrossRef Dhawan A, Kayani MA, Parry JM, Parry E, Anderson D (2003) Aneugenic and clastogenic effects of doxorubicin in human lymphocytes. Mutagenesis 18(6):487–490PubMedCrossRef
34.
35.
go back to reference Kaneko T, Tahara S, Matsuo M (1996) Non-linear accumulation of 8-hydroxy-2′-deoxyguanosine, a marker of oxidized DNA damage, during aging. Mutat Res 316(5–6):277–285PubMedCrossRef Kaneko T, Tahara S, Matsuo M (1996) Non-linear accumulation of 8-hydroxy-2′-deoxyguanosine, a marker of oxidized DNA damage, during aging. Mutat Res 316(5–6):277–285PubMedCrossRef
36.
37.
go back to reference Valavanidis A, Vlachogianni T, Fiotakis C (2009) 8-hydroxy-2′ -deoxyguanosine (8-OHdG): a critical biomarker of oxidative stress and carcinogenesis. J Environ Sci Health, Part C Environ Carcinog Ecotoxicol Rev 27(2):120–139. doi:10.1080/10590500902885684 CrossRef Valavanidis A, Vlachogianni T, Fiotakis C (2009) 8-hydroxy-2′ -deoxyguanosine (8-OHdG): a critical biomarker of oxidative stress and carcinogenesis. J Environ Sci Health, Part C Environ Carcinog Ecotoxicol Rev 27(2):120–139. doi:10.​1080/​1059050090288568​4 CrossRef
38.
go back to reference Grankvist K, Henriksson R (1987) Doxorubicin and epirubicin iron-induced generation of free radicals in vitro. A comparative study. Biosci Rep 7(8):653–658PubMedCrossRef Grankvist K, Henriksson R (1987) Doxorubicin and epirubicin iron-induced generation of free radicals in vitro. A comparative study. Biosci Rep 7(8):653–658PubMedCrossRef
Metadata
Title
Impact of dexrazoxane on doxorubicin-induced aneuploidy in somatic and germinal cells of male mice
Authors
S. M. Attia
S. F. Ahmad
S. A. Bakheet
Publication date
01-01-2016
Publisher
Springer Berlin Heidelberg
Published in
Cancer Chemotherapy and Pharmacology / Issue 1/2016
Print ISSN: 0344-5704
Electronic ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-015-2925-2

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