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首页> 外文期刊>The American Journal of Human Genetics >Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage
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Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage

机译:通过调节对DNA损伤的响应,长时间的Noncoding RNAS丘比特1和丘比特2在11Q13中介导乳腺癌风险

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摘要

Breast cancer risk is strongly associated with an intergenic region on 11q13. We have previously shown that the strongest risk-associated SNPs fall within a distal enhancer that regulates CCND1. Here, we report that, in addition to regulating CCND1, this enhancer regulates two estrogen-regulated long noncoding RNAs, CUPID1 and CUPID2. We provide evidence that the risk-associated SNPs are associated with reduced chromatin looping between the enhancer and the CUPID1 and CUPID2 bidirectional promoter. We further show that CUPID1 and CUPID2 are predominantly expressed in hormone-receptor-positive breast tumors and play a role in modulating pathway choice for the repair of double-strand breaks. These data reveal a mechanism for the involvement of this region in breast cancer.
机译:乳腺癌风险与11Q13的非基因区域强烈相关。 我们之前已经表明,最强烈的风险相关的SNP落在扩大CCND1的远端增强器内。 在这里,我们报告说,除了调节CCND1之外,该增强剂还调节两个雌激素调节的长度非编码RNA,丘比特1和丘比特2。 我们提供了有证据表明风险相关的SNP与增强剂和丘比特1和丘比特2双向启动子之间的染色质环菌还原相关。 我们进一步表明,丘比特1和丘比特在激素受体阳性乳腺肿瘤中主要表达,并在调节双链断裂的调节途径选择中发挥作用。 这些数据揭示了该地区在乳腺癌中的参与的机制。

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