Meiotic stage-dependent induction of chromosome aberrations in Chinese hamster primary oocytes exposed to topoisomerase II inhibitor etoposide

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 476, Issue 1-2, 2001, Pages 139-148

  Tateno, Hiroyuki ^a   Kamiguchi, Yujiroh ^a  

^a ASAHIKAWA MEDICAL COLLEGE   (Japan)

Author keywords

Chinese hamsters; Chromosome aberrations; Etoposide; Oocytes; Topoisomerase II inhibitor

Indexed keywords

CHORIONIC GONADOTROPIN; ETOPOSIDE;

AGED; ANEUPLOIDY; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CHINESE HAMSTER; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME STRUCTURE; CONTROLLED STUDY; FEMALE; MEIOSIS; METAPHASE; NONHUMAN; OOCYTE; PRIORITY JOURNAL; REACTION TIME; TELOPHASE;

ANEUPLOIDY; ANIMALS; CHROMOSOME ABERRATIONS; CRICETINAE; CRICETULUS; DNA TOPOISOMERASES, TYPE II; ENZYME INHIBITORS; ETOPOSIDE; FEMALE; MEIOSIS; METAPHASE; OOCYTES;

CRICETINAE; CRICETULUS GRISEUS; MAMMALIA;

EID: 0035832354     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0027-5107(01)00101-4     Document Type: Article

References (30)

1. Distribution of aneuploidy in human gametes: Comparison between human sperm and oocytes
2. The chromosome complement of human gametes
3. Chromosomally abnormal gametes as a cause of developmental and congenital anomalies in humans
4. Benomyl-induced aneuploidy in mouse oocytes
5. Pattern and frequency of nondisjunction in oocytes from the Djungarian hamster are determined by the stage of first meiotic spindle inhibition
6. Carbendazim (MBC) disrupts oocyte spindle function and induces aneuploidy in hamsters exposed during fertilization (meiosis II)
7. An experimental approach to the analysis of mechanism of meiotic nondisjunction and anaphase lagging in primary oocytes
8. Preferencial nondisjunction of specific bivalents in oocytes from Djungarian hamsters (Phodopus sungorus) following colchicine treatment
9. Oocytes from young and old mice respond differently to colchicine
10. Differential sensitivity of mouse oocytes to colchicine-induced aneuploidy
11. Griseofulvin-induced aneuploidy and meiotic delay in female mouse germ cells. I. Cytogenetic analysis of metaphase II oocytes
12. Nocodazole sensitivity, age-related aneuploidy and alteration in the cell cycle during maturation of mouse oocytes
13. Induction of aneuploidy in Chinese hamster oocytes following in vivo treatments with trimethoxybenzoic compounds and their analogues
14. Meiotic arrest and aneuploidy induced by vinblastine in mouse oocytes
15. Aneuploid-induction in mouse oocytes following exposure to vinblastine-sulfate, pyrimethamine, diethylstilbesterol diphosphate, or chloral hydrate
16. Taxol-induced meiotic maturation delay, spindle defects, and aneuploidy in mouse oocytes and zygotes
17. Preferential pericentric lesions and aneuploidy induced in mouse oocytes by the topoisomerase II inhibitor etoposide
18. Numerical and structural chromosome aberrations induced by etoposide (VP-16) during oocyte maturation of mice: Transmission to one-cell zygotes and damage to dictyate oocytes
19. DNA topoisomerases
20. DNA topoisomerase poisons as antitumor drugs
21. A stable superovulation method in the Chinese hamster with successive administration of PMSG
22. A new assessment system for chromosomal mutagenicity using oocytes and early zygotes of the Chinese hamster
23. Topoisomerase II is a structural component of mitotic chromosome scaffolds
24. Metaphase chromosome structure: Involvement of topoisomerase II
25. DNA topoisomerase IIα is the major chromosome protein recognized by the mitotic phosphoprotein antibody MPM-2
26. Cell cycle-coupled relocation of types I and II topoisomerases and modulation of catalytic enzyme activities
27. First meiotic division abnormalities in human oocytes: Mechanism of trisomy formation
28. Topoisomerase IIα is associated with the mammalian centromere in a cell cycle- and species-specific manner and is required for proper centromere/kinetochore structure
29. SMC proteins and chromosome structure
30. Sister-chromatid separation at anaphase onset is promoted by cleavage of the cohesin subunit Scc 1