Literature DB >> 2475796

Vinblastine, cisplatin and bleomycin (VPB) adjuvant therapy does not induce dose-dependent damage in human chromosomes.

S Gundy1, M Baki, I Bodrogi.   

Abstract

Chromosome aberrations and sister chromatid exchanges were examined in testicular tumor patients treated by 4 cycles of vinblastine, cisplatin and bleomycin adjuvant therapy. The predominant aberrations in cells varied among the patients, and due to interindividual variability no time- or dose-dependent changes were observed in cytogenetic data. There was found an overdispersion of aberrations which might be explained by the effect of bleomycin. Sister chromatid exchange (SCE) frequency was slightly increased and showed also an individual variability in the response to vinblastine, cisplatin and bleomycin (VPB) therapy. No correlation with chromosome aberration rate was found. Further data are required for the real estimation of long-term effects of VPB therapy.

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Year:  1989        PMID: 2475796

Source DB:  PubMed          Journal:  Neoplasma        ISSN: 0028-2685            Impact factor:   2.575


  2 in total

1.  Assessment of genotoxicity of vincristine, vinblastine and vinorelbine in human cultured lymphocytes: a comparative study.

Authors:  N M Mhaidat; K H Alzoubi; O F Khabour; K Z Alawneh; L A Raffee; E S Alsatari; E I Hussein; K E Bani-Hani
Journal:  Balkan J Med Genet       Date:  2016-08-02       Impact factor: 0.519

2.  Synthetic lethality across normal tissues is strongly associated with cancer risk, onset, and tumor suppressor specificity.

Authors:  Kuoyuan Cheng; Nishanth Ulhas Nair; Joo Sang Lee; Eytan Ruppin
Journal:  Sci Adv       Date:  2021-01-01       Impact factor: 14.136

  2 in total

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