Comet assay responses in human lymphocytes are not influenced by the menstrual cycle: a study in healthy Indian females

被引:60
作者
Bajpayee, M [1 ]
Pandey, AK [1 ]
Parmar, D [1 ]
Mathur, N [1 ]
Seth, PK [1 ]
Dhawan, A [1 ]
机构
[1] Ind Toxicol Res Ctr, Div Dev Toxicol, Lucknow 226001, Uttar Pradesh, India
关键词
Indian female population; menstrual cycle; DNA damage; JM-1and MCF-7 cell lines; comet assay;
D O I
10.1016/j.mrgentox.2004.10.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The single-cell gel electrophoresis or Comet assay measures qualitative and quantitative DNA damage in single cells. Its simplicity and non-invasive nature has made it widely accepted for the monitoring of human genotoxicity, employing peripheral blood lymphocytes. Factors, such as gender, age, and dietary and smoking habits are known to affect the Comet assay responses in lymphocytes. However, there is no information regarding the influence of the menstrual cycle on the results of the assay in lymphocytes of females. A study was therefore undertaken among 18 healthy Indian female volunteers to assess the effect of the menstrual cycle on Comet assay responses. During a complete menstrual cycle, only minor changes were observed in the basal levels of DNA damage in the lymphocytes as evident by Comet parameters, such as tail length (mum), tail DNA (%) and Olive tail moment (arbitrary units). To assess the effect of the estrogen 17beta-estradiol (at physiological concentrations of 0.5, 1.0 and 2.0 nM) on the Comet assay responses, an in vitro study was conducted in the human lymphocyte cell line JM-1 and the breast cancer cell line MCF-7. As was evident from the Comet parameters, a significant (p < 0.01) concentration-dependent increase in the level of DNA damage was observed in the MCF-7 cells while no significant change was found in the JM-1 cells. The results indicate that the menstrual cycle does not influence the Comet assay responses in lymphocytes; hence, these can serve as a model for monitoring genotoxicity in females. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 172
页数:10
相关论文
共 48 条
[1]  
ABLIN RJ, 1978, CANCER RES, V38, P3702
[2]  
ABLIN RJ, 1974, J IMMUNOL, V113, P705
[3]   Genotoxic effects of estradiol-17β on human lymphocyte chromosomes [J].
Ahmad, ME ;
Shadab, GGHA ;
Hoda, A ;
Afzal, M .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2000, 466 (01) :109-115
[4]   Oestrogenic compounds and oxidative stress (in human sperm and lymphocytes in the Comet assay) [J].
Anderson, D ;
Schmid, TE ;
Baumgartner, A ;
Cemeli-Carratala, E ;
Brinkworth, MH ;
Wood, JM .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2003, 544 (2-3) :173-178
[5]   Assessment of vinyl chloride-induced DNA damage in lymphocytes of plastic industry workers using a single-cell gel electrophoresis technique [J].
Awara, WM ;
El-Nabi, SH ;
El-Gohary, M .
TOXICOLOGY, 1998, 128 (01) :9-16
[6]   Gender-related differences in basal DNA damage in lymphocytes of a healthy Indian population using the alkaline Comet assay [J].
Bajpayee, M ;
Dhawan, A ;
Parmar, D ;
Pandey, AK ;
Mathur, N ;
Seth, PK .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 520 (1-2) :83-91
[7]  
Barkhem Tomas, 2004, Am J Pharmacogenomics, V4, P19, DOI 10.2165/00129785-200404010-00003
[8]   ASSESSMENT OF DNA-DAMAGE IN LEUKOCYTES FROM INFECTED AND MALNOURISHED CHILDREN BY SINGLE-CELL GEL-ELECTROPHORESIS COMET ASSAY [J].
BETANCOURT, M ;
ORTIZ, R ;
GONZALEZ, C ;
PEREZ, P ;
CORTES, L ;
RODRIGUEZ, L ;
VILLASENOR, L .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1995, 331 (01) :65-77
[9]   COMPARATIVE-STUDIES BY COMET TEST AND SCE ANALYSIS IN HUMAN-LYMPHOCYTES FROM 200 HEALTHY-SUBJECTS [J].
BETTI, C ;
DAVINI, T ;
GIANNESSI, L ;
LOPRIENO, N ;
BARALE, R .
MUTATION RESEARCH-GENETIC TOXICOLOGY, 1995, 343 (04) :201-207
[10]   MICROGEL ELECTROPHORESIS ASSAY (COMET TEST) AND SCE ANALYSIS IN HUMAN-LYMPHOCYTES FROM 100 NORMAL SUBJECTS [J].
BETTI, C ;
DAVINI, T ;
GIANNESSI, L ;
LOPRIENO, N ;
BARALE, R .
MUTATION RESEARCH, 1994, 307 (01) :323-333