Genetic Variation of hTERT, Leukocyte Telomere Length and the Risk of Breast Cancer: A Case-Control Study in Egyptian Females

S. E. E. Feky, Fawziya A. R. Ibrahim, Medhat A. Haroun, Mohammad Abdel-Rahman Ahmmad, M. Elnaggar, Safaa Elghandour, N. A. E. Moneim
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Abstract

Background: hTERT is a key player in telomere biology and its activity is directly related to cell senescence and development of many health-related problems including cancer. Although previous studies investigated this association, the results greatly vary among populations. This study aimed to investigate the association of hTERT gene SNPs and the risk of breast cancer (BC) in Egyptian females and their impact on telomere length (TL). Methods: 218 BC patients and 178 age-matched healthy females were genotyped for hTERT variants rs2736098G > A, rs2735940C > T using PCR-RFLP and for MNS16A tandem repeat using PCR to determine their association with breast cancer risk. Telomere length was measured using qPCR. Results: hTERT rs2736098G > A results indicated that both AG and GG genotypes and G allele were associated with an increased risk of BC. The rs2735940 TT genotype was significantly associated with BC risk, however, the MNS16A tandem repeat region polymorphism didn’t show any correlation with the risk of developing BC. TL showed a significant reduction in BC patients with age < 40 years compared with controls. However, it didn’t show a significant difference above the age of 40 years. Conclusions: hTERT rs2736098 and rs27365940, not MNS16A may be associated with an increased risk of developing BC in Egyptian females. Also, telomere length can be a promising screening marker of BC especially in young population.
遗传变异的hTERT,白细胞端粒长度和乳腺癌的风险:在埃及女性病例对照研究
背景:hTERT是端粒生物学中的关键角色,其活性与细胞衰老和包括癌症在内的许多健康问题的发展直接相关。尽管之前的研究调查了这种关联,但不同人群的结果差异很大。本研究旨在探讨hTERT基因SNPs与埃及女性患癌症(BC)风险的关系及其对端粒长度(TL)的影响。方法:对218例BC患者和178例年龄匹配的健康女性进行hTERT变异体rs2736098G>A、rs2735940C>T的PCR-RFLP基因分型和MNS16A串联重复序列的PCR基因分型,以确定其与癌症风险的关系。使用qPCR测量端粒长度。结果:hTERT rs2736098G>A结果表明,AG和GG基因型及G等位基因均与BC风险增加有关。rs2735940 TT基因型与BC风险显著相关,而MNS16A串联重复区多态性与患BC的风险没有任何相关性。与对照组相比,年龄<40岁的BC患者的TL显著降低。然而,在40岁以上的人群中并没有显示出显著的差异。结论:hTERT rs2736098和rs27365940,而不是MNS16A可能与埃及女性患BC的风险增加有关。此外,端粒长度可能是一个很有前途的BC筛查标志物,尤其是在年轻人群中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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