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位于间皮素启动子区域的rs2235503 C>A变异影响间皮素转录速率及可溶性间皮素相关肽的血浆水平。

Variation rs2235503 C > A Within the Promoter of Affects Transcriptional Rate of Mesothelin and Plasmatic Levels of the Soluble Mesothelin-Related Peptide.

作者信息

Silvestri Roberto, Pucci Perla, De Santi Chiara, Dell'Anno Irene, Miglietta Simona, Corrado Alda, Nicolí Vanessa, Marolda Daniela, Cipollini Monica, Pellegrino Enrica, Evangelista Monica, Bonotti Alessandra, Foddis Rudy, Cristaudo Alfonso, Landi Stefano, Gemignani Federica

机构信息

Department of Biology, University of Pisa, Pisa, Italy.

Division of Cellular and Molecular Pathology, Department of Pathology, University of Cambridge, Cambridge, United Kingdom.

出版信息

Front Genet. 2020 Aug 18;11:975. doi: 10.3389/fgene.2020.00975. eCollection 2020.

Abstract

Soluble mesothelin-related peptide (SMRP) is a promising biomarker for malignant pleural mesothelioma (MPM), but several confounding factors can reduce SMRP-based test's accuracy. The identification of these confounders could improve the diagnostic performance of SMRP. In this study, we evaluated the sequence of 1,000 base pairs encompassing the minimal promoter region of the gene to identify expression quantitative trait loci (eQTL) that can affect SMRP. We assessed the association between four promoter variants and SMRP levels in a cohort of 72 MPM and 677 non-MPM subjects, and we carried out assays to investigate their functional role. Our results show that rs2235503 is an eQTL for associated with increased levels of SMRP in non-MPM subjects. Furthermore, we show that this polymorphic site affects the accuracy of SMRP, highlighting the importance of evaluating the individual's genetic background and giving novel insights to refine SMRP specificity as a diagnostic biomarker.

摘要

可溶性间皮素相关肽(SMRP)是恶性胸膜间皮瘤(MPM)一种很有前景的生物标志物,但一些混杂因素会降低基于SMRP检测的准确性。识别这些混杂因素可提高SMRP的诊断性能。在本研究中,我们评估了包含该基因最小启动子区域的1000个碱基对序列,以识别可能影响SMRP的表达数量性状位点(eQTL)。我们在一个由72例MPM患者和677例非MPM受试者组成的队列中评估了四个启动子变体与SMRP水平之间的关联,并进行了实验以研究它们的功能作用。我们的结果表明,rs2235503是与非MPM受试者中SMRP水平升高相关的基因的一个eQTL。此外,我们表明这个多态性位点会影响SMRP的准确性,凸显了评估个体遗传背景的重要性,并为优化SMRP作为诊断生物标志物的特异性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ce/7461867/4e10833d9a67/fgene-11-00975-g001.jpg

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