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新型 miRNA 多态性与智利人群胃癌的相关性研究。

Novel Risk Associations between microRNA Polymorphisms and Gastric Cancer in a Chilean Population.

机构信息

Advanced Center for Chronic Diseases, Pontificia Universidad Católica de Chile, Santiago 8330034, Chile.

Department of Hematology-Oncology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago 8330034, Chile.

出版信息

Int J Mol Sci. 2021 Dec 31;23(1):467. doi: 10.3390/ijms23010467.

Abstract

Gastric cancer (GC) is the fifth leading cause of cancer deaths in the world, with variations across geographical regions and ethnicities. Emerging evidence indicates that miRNA expression is dysregulated in GC and its polymorphisms may contribute to these variations, which has yet to be explored in Latin American populations. In a case-control study of 310 GC patients and 311 healthy donors from Chile, we assessed the association of 279 polymorphisms in 242 miRNA genes. Two novel polymorphisms were found to be associated with GC: rs4822739:C>G (miR-548j) and rs701213:T>C (miR-4427). Additionally, rs1553867776:T>TCCCCA (miR-4274) and rs12416605:C>T (miR-938) were associated with intestinal-type GC, and rs4822739:C>G (miR-548j) and rs1439619:T>G (miR-3175) with TNM I-II stage. The polymorphisms rs6149511:T> TGAAGGGCTCCA (miR-6891), rs404337:G>A (miR-8084), and rs1439619:T>G (miR-3175) were identified among -infected GC patients and rs7500280:T>C (miR-4719) and rs1439619:T>G (miR-3175) were found among PAI+ infected GC cases. Prediction analysis suggests that seven polymorphisms could alter the secondary structure of the miRNA, and the other one is located in the seed region of miR-938. Targets of miRNAs are enriched in GC pathways, suggesting a possible biological effect. In this study, we identified seven novel associations and replicated one previously described in Caucasian population. These findings contribute to the understanding of miRNA genetic polymorphisms in the GC pathogenesis.

摘要

胃癌(GC)是全球第五大癌症死亡原因,在地理区域和种族之间存在差异。新出现的证据表明,miRNA 的表达在 GC 中失调,其多态性可能导致这些变化,但在拉丁美洲人群中尚未得到探索。在一项来自智利的 310 例 GC 患者和 311 例健康对照的病例对照研究中,我们评估了 242 个 miRNA 基因中的 279 个多态性与 GC 的关联。发现两个新的多态性与 GC 相关:rs4822739:C>G(miR-548j)和 rs701213:T>C(miR-4427)。此外,rs1553867776:T>TCCCCA(miR-4274)和 rs12416605:C>T(miR-938)与肠型 GC 相关,rs4822739:C>G(miR-548j)和 rs1439619:T>G(miR-3175)与 TNM I-II 期相关。多态性 rs6149511:T>TGAAGGGCTCCA(miR-6891)、rs404337:G>A(miR-8084)和 rs1439619:T>G(miR-3175)在 GC 患者中被鉴定出来,rs7500280:T>C(miR-4719)和 rs1439619:T>G(miR-3175)在 PAI+感染的 GC 病例中被发现。预测分析表明,七个多态性可能改变 miRNA 的二级结构,另一个位于 miR-938 的种子区。miRNA 的靶标在 GC 途径中富集,表明可能存在生物学效应。在这项研究中,我们确定了七个新的关联,并复制了一个在白种人群中描述的关联。这些发现有助于理解 miRNA 遗传多态性在 GC 发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8304/8745138/1ba62e0df192/ijms-23-00467-g001.jpg

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