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一种罕见的非洲血统变异通过调节癌症相关增强子激活 8q24 lncRNA 枢纽。

A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer.

机构信息

Genetics and Development, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, Karnataka, 560065, India.

Sastra Deemed University, Thanjavur, Tamil Nadu, 613401, India.

出版信息

Nat Commun. 2020 Jul 17;11(1):3598. doi: 10.1038/s41467-020-17325-y.

Abstract

Genetic variation at the 8q24 locus is linked with the greater susceptibility to prostate cancer in men of African ancestry. One such African ancestry specific rare variant, rs72725854 (A>G/T) (~6% allele frequency) has been associated with a ~2-fold increase in prostate cancer risk. However, the functional relevance of this variant is unknown. Here we show that the variant rs72725854 is present in a prostate cancer-specific enhancer at 8q24 locus. Chromatin-conformation capture and dCas9 mediated enhancer blocking establish a direct regulatory link between this enhancer and lncRNAs PCAT1, PRNCR1 and PVT1. The risk allele ('T') is associated with higher expression of PCAT1, PVT1 and c-myc in prostate tumors. Further, enhancer with the risk allele gains response to androgen stimulation by recruiting the transcription factor SPDEF whereas, non-risk alleles remain non-responsive. Elevated expression of these lncRNAs and c-myc in risk allele carriers may explain their greater susceptibility to prostate cancer.

摘要

8q24 位置的遗传变异与非洲裔男性前列腺癌的更高易感性有关。一种非洲裔特异性罕见变异 rs72725854(A>G/T)(~6%等位基因频率)与前列腺癌风险增加约 2 倍有关。然而,该变体的功能相关性尚不清楚。在这里,我们表明变体 rs72725854 存在于 8q24 位置的前列腺癌特异性增强子中。染色质构象捕获和 dCas9 介导的增强子阻断建立了该增强子与 lncRNA PCAT1、PRNCR1 和 PVT1 之间的直接调节联系。风险等位基因(“T”)与前列腺肿瘤中 PCAT1、PVT1 和 c-myc 的更高表达相关。此外,具有风险等位基因的增强子通过募集转录因子 SPDEF 对雄激素刺激产生反应,而非风险等位基因仍然没有反应。这些 lncRNA 和 c-myc 在风险等位基因携带者中的表达升高可能解释了他们对前列腺癌的更高易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca2/7368061/088a87a82d59/41467_2020_17325_Fig1_HTML.jpg

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