首页> 外文期刊>Advances in Breast Cancer Research >Genetic Variation of &i&hTERT&/i&, Leukocyte Telomere Length and the Risk of Breast Cancer: A Case-Control Study in Egyptian Females
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Genetic Variation of &i&hTERT&/i&, Leukocyte Telomere Length and the Risk of Breast Cancer: A Case-Control Study in Egyptian Females

机译:hTERT / i的遗传变异,白细胞端粒长度和乳腺癌风险:埃及女性的病例对照研究

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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.
机译:背景:hTERT是端粒生物学的关键参与者,其活性与细胞衰老以及许多与健康相关的问题(包括癌症)的发展直接相关。尽管先前的研究调查了这种关联,但结果在人群之间差异很大。这项研究旨在研究埃及女性中 hTERT基因SNP与乳腺癌风险(BC)及其对端粒长度(TL)的影响。 方法:使用PCR-RFLP对218名BC患者和178名年龄相匹配的健康女性进行hTERT变体rs2736098G> A,rs2735940C> T的基因分型,并通过PCR对MNS16A串联重复进行基因分型,以确定其与乳腺癌风险的关联。使用 qPCR测量端粒长度。 结果: hTERT rs2736098G>结果表明AG和GG基因型以及G等位基因均与BC风险增加相关。 rs2735940 TT基因型与BC风险显着相关,但是MNS16A串联重复序列多态性与BC风险无关。与对照组相比,TL显示年龄<40岁的BC患者明显减少。但是,在40岁以上的人群中并没有显着差异。 结论: hTERT rs2736098和rs27365940而非MNS16A可能与埃及女性罹患BC的风险增加有关。同样,端粒长度可能是BC的有前途的筛选标志,尤其是在年轻人中。

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