Chromosome aberrations induced by etoposide (VP‐16) are not random
- 15 November 1990
- journal article
- research article
- Published by Wiley in International Journal of Cancer
- Vol. 46 (5), 808-812
- https://doi.org/10.1002/ijc.2910460511
Abstract
The clastogenic effect of etoposide, an anti‐cancer chemotherapeutic drug, was investigated in vitro on lymphocytes of 5 healthy donors. The analysis of the first division metaphases arising after mutagenesis in G1, phase shows that chromosome‐type aberrations are much more frequent than chromatid‐type lesions. The distribution in relation to chromosome lengths of the 439 breakpoints that were accurately identified is not random: chromosomes I, II and 17 are most frequently involved, while chromosomes 4, 5 and × are seldom affected. This non‐random distribution may be related to chromosome structure, since R‐band‐rich chromosomes are significantly more affected than G‐band‐rich chromosomes.This publication has 19 references indexed in Scilit:
- Chromosomal differences between acute nonlymphocytic leukemia in patients with prior solid tumors and prior hematologic malignanciesCancer Genetics and Cytogenetics, 1989
- Specific Sites of Chromosomal Radiation-induced RearrangementsPublished by Elsevier ,1989
- The chemotherapeutic drug melphalan induces breakage of chromosomes regions rearranged in secondary leukemiaCancer Genetics and Cytogenetics, 1989
- Topoisomerase II: A specific marker for cell proliferation.The Journal of cell biology, 1986
- Detecting abnormal human chromosome constitutions by dual laser flow cytogeneticsAmerican Journal of Medical Genetics, 1986
- DNA topoisomerases from rat liver: physiological variationsNucleic Acids Research, 1983
- Frequency and distribution studies of asymmetrical versus symmetrical chromosome aberrationsMutation Research, 1982
- Localization of γ-rays induced chromatid breaks using a three consecutive staining-techniqueMutation Research, 1978
- Systematic analysis of 95 reciprocal translocations of autosomesHuman Genetics, 1978
- Localization of chromatid breaks in Fanconi's anemia, using three consecutive stainsHuman Genetics, 1977