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微小RNA-126在消化系统癌症中的新作用:从实验台到病床边

Novel role of microRNA-126 in digestive system cancers: From bench to bedside.

作者信息

Hu Mingli, Xiong Shengwei, Chen Qiaofeng, Zhu Shixuan, Zhou Xiaodong

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330000, P.R. China.

出版信息

Oncol Lett. 2019 Jan;17(1):31-41. doi: 10.3892/ol.2018.9639. Epub 2018 Oct 29.

DOI:10.3892/ol.2018.9639
PMID:30655735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6313097/
Abstract

MicroRNAs (miRNAs) are ubiquitously expressed, small, non-coding RNAs that regulate the expression of approximately 30% of the human genes at the post-transcriptional level. miRNAs have emerged as crucial modulators in the initiation and progression of various diseases, including numerous cancer types. The high incidence rate of cancer and the large number of cancer-associated cases of mortality are mostly due to a lack of effective treatments and biomarkers for early diagnosis. Therefore there is an urgent requirement to further understand the underlying mechanisms of tumorigenesis. MicroRNA-126 (miR-126) is significantly downregulated in a number of tumor types and is commonly identified as a tumor suppressor in digestive system cancers (DSCs). miR-126 downregulates various oncogenes, including disintegrin and metalloproteinase domain-containing protein 9, v-crk sarcoma virus CT10 oncogene homolog and phosphoinositide-3-kinase regulatory subunit 2. These genes are involved in a number of tumor-associated signaling pathways, including angiogenesis, epithelial-mensenchymal transition and metastasis pathways. The aim of the current review was to summarize the role of miR-126 in DSCs, in terms of its dysregulation, target genes and associated signaling pathways. In addition, the current review has discussed the potential clinical application of miR-126 as a biomarker and therapeutic target for DSCs.

摘要

微小RNA(miRNA)是普遍表达的小非编码RNA,在转录后水平调节约30%的人类基因的表达。miRNA已成为包括多种癌症类型在内的各种疾病发生和发展的关键调节因子。癌症的高发病率和大量与癌症相关的死亡病例主要是由于缺乏有效的治疗方法和早期诊断的生物标志物。因此,迫切需要进一步了解肿瘤发生的潜在机制。微小RNA-126(miR-126)在多种肿瘤类型中显著下调,在消化系统癌症(DSC)中通常被确定为肿瘤抑制因子。miR-126下调多种癌基因,包括含去整合素和金属蛋白酶结构域蛋白9、v-crk肉瘤病毒CT10癌基因同源物和磷脂酰肌醇-3-激酶调节亚基2。这些基因参与多种与肿瘤相关的信号通路,包括血管生成、上皮-间质转化和转移通路。本综述的目的是总结miR-126在DSC中的作用,包括其失调、靶基因和相关信号通路。此外,本综述还讨论了miR-126作为DSC的生物标志物和治疗靶点的潜在临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a2/6313097/60f87bc666ca/ol-17-01-0031-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a2/6313097/ddfce80d4918/ol-17-01-0031-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a2/6313097/60f87bc666ca/ol-17-01-0031-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a2/6313097/ddfce80d4918/ol-17-01-0031-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a2/6313097/60f87bc666ca/ol-17-01-0031-g01.jpg

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Dysregulation of miR-126/Crk protein axis predicts poor prognosis in gastric cancer patients.
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