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基于靶向测序的非侵入性结直肠腺瘤潜在循环 mRNA 标志物

Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing.

机构信息

Department of Health Technology and Informatics, Faculty of Health and Social Sciences, Hong Kong Polytechnic University, Kowloon, Hong Kong, China.

Department of Surgery, Queen Elizabeth Hospital, Kowloon, Hong Kong, China.

出版信息

Sci Rep. 2019 Sep 10;9(1):12943. doi: 10.1038/s41598-019-49445-x.

Abstract

We have developed an optimized protocol for plasma targeted mRNA sequencing in our previous study. Here, we performed plasma targeted mRNA sequencing for 40 colorectal adenoma patients and 39 colonoscopy-proven normal controls in order to find potential circulating mRNA markers for colorectal adenoma. Results showed that GSK3A and RHOA were differential expressed genes identified by a cut-off of fold change >2 and adjusted P value < 0.05. More detailed analysis showed that the expression of both GSK3A (0.01-fold with adjusted P < 1 × 10) and RHOA (0.35-fold with adjusted P < 0.01) in adenoma patients was significantly lower than those in normal healthy subjects. Based on the enrichment analysis of biological process for potential markers, we found that the regulation of programmed cell death (GO: 0043067; GO: 0043069), regulation of cell death (GO: 0010941; GO: 0060548) and cell differentiation (GO: 0021861) were the main processes involved in adenoma formation. In summary, this study is a cutting-edge research on the detection of plasma mRNA in colorectal adenoma patients and normal healthy subjects.

摘要

我们在之前的研究中已经开发出一种优化的血浆靶向 mRNA 测序方案。在这里,我们对 40 例结直肠腺瘤患者和 39 例经结肠镜证实的正常对照进行了血浆靶向 mRNA 测序,以寻找结直肠腺瘤的潜在循环 mRNA 标志物。结果表明,GSK3A 和 RHOA 是通过倍数变化>2 和调整后的 P 值<0.05 筛选出来的差异表达基因。更详细的分析表明,在腺瘤患者中,GSK3A(调整后 P<1×10-1 的 0.01 倍)和 RHOA(调整后 P<0.01 的 0.35 倍)的表达明显低于正常健康受试者。基于对潜在标志物的生物过程富集分析,我们发现程序性细胞死亡的调节(GO:0043067;GO:0043069)、细胞死亡的调节(GO:0010941;GO:0060548)和细胞分化(GO:0021861)是腺瘤形成中涉及的主要过程。总之,本研究是对结直肠腺瘤患者和正常健康对照血浆 mRNA 检测的一项前沿研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c638/6736954/866449fcfe6d/41598_2019_49445_Fig3_HTML.jpg

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