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Genotoxicity of pemetrexed in human peripheral blood lymphocytes

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Abstract

Pemetrexed (PMX) is an antineoplastic antifolate used in the treatment of non-small cell lung cancer, mesothelioma and several types of neoplasms. Its toxicity in tumor cells has been linked with the potent inhibition of thymidylate synthase, dihydrofolate reductase and glycinamide ribonucleotide formyl transferase, and subsequent depletion of both purine and pyrimidine nucleotides. However, cytogenetic toxicity of PMX in non-diseased cells has not been adequately studied; despite the increasing data on the DNA-damaging potential of antineoplastic agents on normal cells. In the present study, the genotoxic potential of PMX was evaluated in peripheral blood lymphocytes obtained from healthy human subjects using chromosome aberration (CA), sister chromatid exchange (SCE) and micronucleus (MN) assays as the cytogenetic damage markers. Human peripheral blood lymphocytes were exposed to four different concentrations (25, 50, 75 and 100 μg/mL) of PMX for 24- and 48-h treatment periods. PMX significantly increased the formation of CA in 24-h treatment, but not in 48-h treatment. PMX did not increase the mean SCE frequency in 24- and 48-h treatment periods; however, there was a striking increase (although not statistically significant, p > 0.05) in the number of SCEs at 25 μg/mL (24- and 48-h treatment) and 50 μg/mL (24-h treatment) due to an increase of SCE at the single-cell level. Interestingly, PMX did not induce MN formation in either 24- or 48-h treatment periods. PMX strongly decreased the mitotic index (MI), proliferation index (PI) and nuclear division index (NDI) in 24- and 48-h treatment periods. Our results suggest that PMX has a potent cytotoxic effect against human peripheral blood lymphocytes at concentrations which are reached in vivo in the blood plasma.

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References

  • Albertini RJ, Anderson D, Douglas GR, Hagmar L, Hemminki K, Merlo F, Natarajan AT, Norppa H, Shuker DE, Tice R, Waters MD, Aitio A (2000) IPCS guidelines for the monitoring of genotoxic effects of carcinogens in humans. Mutat Res 463:111–172

    Article  CAS  Google Scholar 

  • Bender MA, Brewen JG (1969) Factors influencing chromosome aberration yields in the human peripheral leukocyte system. Mutat Res 8:383–399

    Article  CAS  Google Scholar 

  • Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, Wickramasinghe SN, Everson RB, Ames BN (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Natl Acad Sci 94:3290–3295

    Article  CAS  Google Scholar 

  • Chattopadhyay S, Moran RG, Goldman ID (2007) Pemetrexed: biochemical and cellular pharmacology, mechanisms, and clinical applications. Mol Cancer Ther 6:404–417

    Article  CAS  Google Scholar 

  • Choudhury R, Ghosh SK, Palo AK (2000) Cytogenetic toxicity of methotrexate in mouse bone marrow. Environ Toxicol Pharmacol 8:191–196

    Article  CAS  Google Scholar 

  • Choudhury R, Ghosh SK, Palo AK (2001) Potential transmission of the cytogenetic toxic effects of methotrexate in the male germline cells of Swiss mice. Environ Toxicol Pharmacol 10:81–88

    Article  CAS  Google Scholar 

  • Chow M, Koo J, Ng P, Rubin H (1998) Random population-wide genetic damage induced in replicating cells treated with methotrexate. Mutat Res 413:251–264

    Article  CAS  Google Scholar 

  • Dalkic E, Wang X, Wright N, Chan C (2010) Cancer-drug associations: a complex system. PLoS ONE 5:e10031

    Article  Google Scholar 

  • Evans HJ (1984) Human peripheral blood lymphocytes for the analysis of chromosome aberrations in mutagen tests. In: Kilbey BJ, Legator M, Nichols W, Ramel C (eds) Handbook of mutagenicity test procedures, 2nd edn. Elsevier, Amsterdam, pp 405–427

    Google Scholar 

  • Fenech M (2000) The in vitro micronucleus technique. Mutat Res 455:81–95

    Article  CAS  Google Scholar 

  • Hittelman WN (1973) The type and time of occurrence of aminopterin-induced chromosome aberrations in cultured potorous cells. Mutat Res 18:93–102

    Article  CAS  Google Scholar 

  • Jensen MK, Nyfors A (1979) Cytogenetic effects of methotrexate on human cells in vivo: comparison between results obtained by chromosome studies on bone-marrow cells and blood lymphocytes and by the micronucleus test. Mutat Res 64:339–343

    Article  CAS  Google Scholar 

  • Kao SCH, Phan VH, Clarke SJ (2010) Predictive markers for haematological toxicity of pemetrexed. Curr Drug Targets 11:48–57

    Article  CAS  Google Scholar 

  • Kasahara Y, Nakai Y, Miura D, Yagi K, Hirabayashi K, Makita T (1992a) Mechanism of induction of micronuclei and chromosome aberrations in mouse bone marrow by multiple treatments of methotrexate. Mutat Res 278:145–151

    Article  CAS  Google Scholar 

  • Kasahara Y, Wakata A, Nakai Y, Yuno K, Miura D, Yagi K, Hirabayashi K, Makita T (1992b) The micronucleus test using peripheral blood reticulocytes from methotrexate-treated mice. Mutat Res 280:117–128

    Article  CAS  Google Scholar 

  • Kelsey KT, Wiencke JK, Eisen EA, Lynch DW, Lewis TR, Little JB (1988) Persistently elevated sister chromatid exchanges in ethylene oxide-exposed primates: the role of a subpopulation of high frequency cells. Cancer Res 48:5045–5050

    CAS  Google Scholar 

  • Keshava C, Keshava N, Whong WZ, Nath J, Ong TM (1997) Inhibition of methotrexate-induced chromosomal damage by vanillin and chlorophyllin in V79 cells. Teratog Carcinog Mutagen 17:313–326

    Article  CAS  Google Scholar 

  • Kirsch-Volders M, Sofuni T, Aardema M, Albertini S, Eastmond D, Fenech M, Ishidate M Jr, Lorge E, Norppa H, Surrallés J, von der Hude W, Wakata A (2003) Report from the in vitro micronucleus assay working group. Mutat Res 540:153–163

    Article  CAS  Google Scholar 

  • Lezana EA, Bianchi NO, Bianchi MS, Zabala-Suarez JE (1977) Sister chromatid exchanges in down syndromes and normal human beings. Mutat Res 5:85–90

    Google Scholar 

  • Li JC, Kaminskas E (1984) Accumulation of DNA strand breaks and methotrexate cytotoxicity. Proc Natl Acad Sci 81:5694–5698

    Article  CAS  Google Scholar 

  • Mace ML, Daskal Y, Wray W (1978) Scanning electron microscopy of chromosome aberrations. Mutat Res 52:199–206

    Article  Google Scholar 

  • Paz-y-Miño C, Bustamante G, Sánchez ME, Leone PE (2002) Cytogenetic monitoring in a population occupationally exposed to pesticide in Ecuador. Environ Health Persp 110:1077–1080

    Article  Google Scholar 

  • Perry PE, Thomson EJ (1984) The methodology of sister chromatid exchanges. In: Kilbey BJ, Legator M, Nichols W, Ramel C (eds) Handbook of mutagenicity test procedures, 2nd edn. Elsevier, Amsterdam, pp 459–529

    Google Scholar 

  • Poser RG, Sirotnak FM, Chello PL (1981) Differential synthesis of methotrexate polyglutamates in normal proliferative and neoplastic mouse tissues in vivo. Cancer Res 41:4441–4446

    CAS  Google Scholar 

  • Rothfuss A, Schütz P, Bochum S, Volm T, Eberhardt E, Kreienberg R, Vogel W, Speit G (2000) Induced micronucleus frequencies in peripheral lymphocytes as a screening test for carriers of a BRCA1 mutation in breast cancer families. Cancer Res 60:390–394

    CAS  Google Scholar 

  • Shih C, Habeck LL, Mendelsohn LG, Chen VJ, Schultz RM (1998) Multiple folate enzyme inhibition: mechanism of a novel pyrrolopyrimidine-based antifolate LY231514 (MTA). Advan Enzyme Regul 38:135–152

    Article  CAS  Google Scholar 

  • Smit EF, Mattson K, von Pawel J, Manegold C, Clarke S, Postmus PE (2003) ALIMTA (pemetrexed disodium) as second-line treatment of non-small-cell lung cancer: a phase II study. Ann Oncol 14:455–460

    Article  CAS  Google Scholar 

  • Speit G, Haupter S (1985) On the mechanisms of differential giemsa staining of bromodeoxyuridine-substituted chromosomes. II. Differences between the demonstration of sister chromatid differentiation and replication patterns. Hum Genet 70:126–129

    Article  CAS  Google Scholar 

  • Tonkinson JL, Marder P, Andis SL, Schultz RM, Gossett LS, Shih C, Mendelsohn LG (1997) Cell cycle effects of antifolate antimetabolites: implications for cytotoxicity and cytostasis. Cancer Chemoth Pharm 39:521–531

    Article  CAS  Google Scholar 

  • Tweats DJ, Blakey D, Heflich RH, Jacobs A, Jacobsen SD, Morita T, Nohmi T, O’Donovan MR, Sasaki YF, Sofuni T, Tice R (2007) Report of the IWGT working group on strategy/interpretation for regulatory in vivo tests II. Identification of in vivo-only positive compounds in the bone marrow micronucleus test. Mutat Res 627:92–105

    Article  CAS  Google Scholar 

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Acknowledgments

This work was supported by Cukurova University Research Fund (FEF2011D8).

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Correspondence to Erman Salih İstifli.

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İstifli, E.S., Topaktaş, M. Genotoxicity of pemetrexed in human peripheral blood lymphocytes. Cytotechnology 65, 621–628 (2013). https://doi.org/10.1007/s10616-012-9516-4

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