J Breast Cancer.  2013 Sep;16(3):285-290. 10.4048/jbc.2013.16.3.285.

Cytogenetic Finding of Breast Cancer Cases and in Their First-Degree Relatives

Affiliations
  • 1Department of Medical Biology and Genetic, Suleyman Demirel University School of Medicine, Isparta, Turkey. pinarkosar@sdu.edu.tr
  • 2Department of General Surgery, Suleyman Demirel University Medical Faculty, Isparta, Turkey.

Abstract

PURPOSE
The aim of this study was to evaluate and compare the rate of sister chromatid exchange (SCE), the occurrence of micronuclei, and the lymphocyte proliferation rate index (PRI) in patients with breast cancer, their first-degree relatives, and healthy volunteers.
METHODS
We analyzed the frequency of SCE and micronuclei, and the PRI in the peripheral blood lymphocytes of 30 women with breast cancer, 22 of their female family members, and 20 age-matched healthy female volunteers.
RESULTS
SCE occurred significantly more often in the lymphocytes of breast cancer patients (10.84+/-0.4 per metaphase), compared with their first-degree relatives (7.45+/-0.54) and controls (5.94+/-0.2) (p<0.001 for both). The mean SCE frequency was not statistically different between first-degree relatives and controls (p=0.071). Similarly, micronuclei occurred at a significantly higher rate in breast cancer patients (9.6+/-0.72), and in their first-degree relatives (7+/-0.64), compared to controls (3.85+/-0.4) (p<0.001 and p=0.001, respectively). There was also a significant difference between the occurrence of micronuclei in patients compared to their family members (p=0.021). The PRI was significantly lower in patients (1.61+/-0.1), compared with both their first-degree relatives (1.75+/-0.1), and controls (1.74+/-0.1) (p=0.001 and p=0.002, respectively).
CONCLUSION
Increased SCE and the occurrence of micronuclei, as well as a reduced PRI are associated with breast cancer. Furthermore, increased SCE and the frequency of micronuclei in a first-degree relative suggest that they exhibit greater genetic instability than women of the same age.

Keyword

Breast neoplasms; DNA damage; Germline micronucleus; Sister chromatid exchange

MeSH Terms

Breast
Breast Neoplasms
Cytogenetics
DNA Damage
Female
Humans
Lymphocytes
Micronucleus, Germline
Sister Chromatid Exchange

Reference

1. Sandberg AA. Chromosome abnormalities in human cancer and leukemia. Mutat Res. 1991; 247:231–240.
Article
2. Dhillon VS, Dhillon IK. Chromosome aberrations and sister chromatid exchange studies in patients with prostate cancer: possible evidence of chromosome instability. Cancer Genet Cytogenet. 1998; 100:143–147.
Article
3. Mohana Devi S, Balachandar V, Arun M, Suresh Kumar S, Balamurali Krishnan B, Sasikala K. Analysis of genetic damage and gene polymorphism in hepatocellular carcinoma (HCC) patients in a South Indian population. Dig Dis Sci. 2013; 58:759–767.
Article
4. Albertini RJ, Anderson D, Douglas GR, Hagmar L, Hemminki K, Merlo F, et al. IPCS guidelines for the monitoring of genotoxic effects of carcinogens in humans: International Programme on Chemical Safety. Mutat Res. 2000; 463:111–172.
Article
5. Hagmar L, Bonassi S, Strömberg U, Brøgger A, Knudsen LE, Norppa H, et al. Chromosomal aberrations in lymphocytes predict human cancer: a report from the European Study Group on Cytogenetic Biomarkers and Health (ESCH). Cancer Res. 1998; 58:4117–4121.
6. Bonassi S, Hagmar L, Strömberg U, Montagud AH, Tinnerberg H, Forni A, et al. Chromosomal aberrations in lymphocytes predict human cancer independently of exposure to carcinogens: European Study Group on Cytogenetic Biomarkers and Health. Cancer Res. 2000; 60:1619–1625.
7. Fucić A, Znaor A, Strnad M, van der Hel O, Aleksandrov A, Miskov S, et al. Chromosome damage and cancer risk in the workplace: the example of cytogenetic surveillance in Croatia. Toxicol Lett. 2007; 172:4–11.
Article
8. Dhar PK, Devi S, Rao TR, Kumari U, Joseph A, Kumar MR, et al. Significance of lymphocytic sister chromatid exchange frequencies in ovarian cancer patients. Cancer Genet Cytogenet. 1996; 89:105–108.
Article
9. Dhillon VS, Kler RS, Dhillon IK. Choromosome instabililty and sister chromatid exchange (SCE) studies in patients with carcinoma of cervix uteri. Cancer Genet Cytogenet. 1996; 86:54–57.
Article
10. Dhillon VS, Bhasker R, Kler RS, Husain SA. Sister chromatid exchange (SCE) studies in breast cancer patients: a follow-up study. Cancer Genet Cytogenet. 1995; 80:115–117.
Article
11. Narin A, Tuncay O. Relationships between malignant melanoma and chromosome damage in human peripheral blood lymphocytes. Asian Pac J Cancer Prev. 2012; 13:5229–5232.
Article
12. Gutiérrez-Enríquez S, Ramón Y, Alonso C, Corral A, Carrasco P, Cornet M, et al. Ionizing radiation or mitomycin-induced micronuclei in lymphocytes of BRCA1 or BRCA2 mutation carriers. Breast Cancer Res Treat. 2011; 127:611–622.
Article
13. Barch MJ, Lawce HJ, Arsham MS. Peripheral blood culture. In : Barch MJ, editor. The ACT Cytogenetics Laboratory Manual. 2nd ed. New York: Raven Press;1991. p. 24–30.
14. Perry P, Wolff S. New Giemsa method for the differential staining of sister chromatids. Nature. 1974; 251:156–158.
Article
15. Lamberti L, Bigatti Ponzetto P, Ardito G. Cell kinetics and sister-chromatid-exchange frequency in human lymphocytes. Mutat Res. 1983; 120:193–199.
Article
16. Orta T, Günebakan S. The effect of aging on micronuclei frequency and proliferation in human peripheral blood lymphocytes. Indian J Hum Genet. 2012; 18:95–100.
Article
17. Hoffmann H, Speit G. Assessment of DNA damage in peripheral blood of heavy smokers with the comet assay and the micronucleus test. Mutat Res. 2005; 581:105–114.
Article
18. Nordenson I, Beckman L, Lidén S, Stjernberg N. Chromosomal aberrations and cancer risk. Hum Hered. 1984; 34:76–81.
Article
19. Cortés-Gutiérrez EI, Cerda-Flores RM, Leal-Garza CH. Sister chromatid exchanges in peripheral lymphocytes from women with carcinoma of the uterine cervix. Cancer Genet Cytogenet. 2000; 122:121–123.
Article
20. Baltaci V, Kayikçioğlu F, Alpas I, Zeyneloğlu H, Haberal A. Sister chromatid exchange rate and alkaline comet assay scores in patients with ovarian cancer. Gynecol Oncol. 2002; 84:62–66.
Article
21. Roy SK, Trivedi AH, Bakshi SR, Patel RK, Shukla PH, Patel SJ, et al. Spontaneous chromosomal instability in breast cancer families. Cancer Genet Cytogenet. 2000; 118:52–56.
Article
22. Cefle K, Ucur A, Guney N, Ozturk S, Palanduz S, Tas F, et al. Increased sister chromatid exchange frequency in young women with breast cancer and in their first-degree relatives. Cancer Genet Cytogenet. 2006; 171:65–67.
Article
23. Pastor S, Creus A, Parrón T, Cebulska-Wasilewska A, Siffel C, Piperakis S, et al. Biomonitoring of four European populations occupationally exposed to pesticides: use of micronuclei as biomarkers. Mutagenesis. 2003; 18:249–258.
Article
24. Aristei C, Stracci F, Guerrieri P, Anselmo P, Armellini R, Rulli A, et al. Frequency of sister chromatid exchanges and micronuclei monitored over time in patients with early-stage breast cancer: results of an observational study. Cancer Genet Cytogenet. 2009; 192:24–29.
Article
25. Santos RA, Teixeira AC, Mayorano MB, Carrara HH, Andrade JM, Takahashi CS. Basal levels of DNA damage detected by micronuclei and comet assays in untreated breast cancer patients and healthy women. Clin Exp Med. 2010; 10:87–92.
Article
26. Kopjar N, Milas I, Garaj-Vrhovac V, Gamulin M. Cytogenetic outcomes of adjuvant chemotherapy in non-target cells of breast cancer patients. Hum Exp Toxicol. 2007; 26:391–399.
Article
Full Text Links
  • JBC
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr