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RP11-638I2.4 转录本中的风险 SNP 增加 lncRNA-YY1 相互作用并增加胰腺癌易感性。

Risk SNP in a transcript of RP11-638I2.4 increases lncRNA-YY1 interaction and pancreatic cancer susceptibility.

机构信息

Department of Epidemiology and Biostatistics, Key Laboratory for Environment and Health (Ministry of Education), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

Department of Epidemiology and Biostatistics, School of Public Health, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, 430071, China.

出版信息

Arch Toxicol. 2023 Oct;97(10):2799-2812. doi: 10.1007/s00204-023-03564-7. Epub 2023 Aug 16.

Abstract

Tens of thousands of long non-coding RNAs (lncRNAs) have been identified through RNA-seq analysis, but the biological and pathological significance remains unclear. By integrating the genome-wide lncRNA data with a cross-ancestry meta-analysis of PDAC GWASs, we depicted a comprehensive atlas of pancreatic ductal adenocarcinoma (PDAC)-associated lncRNAs, containing 1,204 lncRNA (445 novel lncRNAs and 759 GENCODE annotated lncRNAs) and 4,368 variants. Furthermore, we found that PDAC-associated lncRNAs could function by altering chromatin activity, transcription factors, and RNA-binding proteins binding affinity. Importantly, genetic variants linked to PDAC are preferentially found at PDAC-associated lncRNA regions, supporting the biological and clinical relevance of PDAC-associated lncRNAs. Finally, we prioritized a novel transcript (MICT00000110172.1) of RP11-638I2.4 as a potential tumor promoter. MICT00000110172.1 is able to reinforce the interaction with YY1, which could reverse the effect of YY1 on pancreatic cancer cell cycle arrest to promote the pancreatic cancer growth. G > A change at rs2757535 in the second exon of MICT00000110172.1 induces a spatial structural change and creates a target region for YY1 binding, which enforces the effect of MICT00000110172.1 in an allele-specific manner, and thus confers susceptibility to tumorigenesis. In summary, our results extend the repertoire of PDAC-associated lncRNAs that could act as a starting point for future functional explorations, and the identification of lncRNA-based target therapy.

摘要

通过 RNA-seq 分析已经鉴定出数万种长链非编码 RNA(lncRNA),但其生物学和病理学意义尚不清楚。通过将全基因组 lncRNA 数据与 PDAC GWAS 的跨血统荟萃分析相结合,我们描绘了一幅胰腺导管腺癌(PDAC)相关 lncRNA 的综合图谱,包含 1204 个 lncRNA(445 个新的 lncRNA 和 759 个 GENCODE 注释的 lncRNA)和 4368 个变体。此外,我们发现 PDAC 相关 lncRNA 可以通过改变染色质活性、转录因子和 RNA 结合蛋白的结合亲和力来发挥作用。重要的是,与 PDAC 相关的遗传变异更倾向于出现在与 PDAC 相关的 lncRNA 区域,这支持了与 PDAC 相关的 lncRNA 的生物学和临床相关性。最后,我们将一种新的转录本(MICT00000110172.1)优先作为潜在的肿瘤促进物。MICT00000110172.1 能够加强与 YY1 的相互作用,从而逆转 YY1 对胰腺癌细胞周期阻滞的作用,促进胰腺癌细胞的生长。MICT00000110172.1 第二外显子中 rs2757535 的 G>A 变化诱导空间结构变化,并创建一个 YY1 结合的靶区,以等位基因特异性的方式强制 MICT00000110172.1 的作用,从而使肿瘤易感性增强。总之,我们的研究结果扩展了与 PDAC 相关的 lncRNA 谱,为未来的功能探索和基于 lncRNA 的靶向治疗提供了起点。

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