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沉默的治疗者:miR-205-5p 的上调通过间接上调 E-钙黏蛋白的表达抑制结肠癌细胞的上皮间质转化。

The silent healer: miR-205-5p up-regulation inhibits epithelial to mesenchymal transition in colon cancer cells by indirectly up-regulating E-cadherin expression.

机构信息

MEDFUTURE - Research Center for Advanced Medicine, "Iuliu-Hatieganu" University of Medicine and Pharmacy, Marinescu 23 Street / Louis Pasteur 4-6 Street, Cluj-Napoca, Romania.

Research Center for Functional Genomics, Biomedicine and Translational Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, 23 Marinescu Street, 400337, Cluj-Napoca, Romania.

出版信息

Cell Death Dis. 2018 Jan 19;9(2):66. doi: 10.1038/s41419-017-0102-8.

DOI:10.1038/s41419-017-0102-8
PMID:29352232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5833765/
Abstract

EMT represents the dominant program within advanced stages of colon cancer, where cells acquire migratory characteristics in order to invade secondary tissues and form metastasis. Where the majority of the therapeutic strategies are concentrated on the reduction of the tumor mass through different apoptotic mechanisms, the present study advocates an important role for miR-205-5p in impairment of colon cancer cells migration and restoration of the epithelial phenotype. Upon identification of a homogenous downregulated profile for miR-205-5p in colon adenocarcinoma patients, functional studies demonstrated that experimental upregulation of this sequence is able to significantly raise the levels of E-cadherin through direct inhibition of ZEB1. Moreover, the elevation in CDH1 expression was translated into functional parameters where cells lost their invasion and migratory characteristics and formed homogenous clusters through adhesion interactions. Survival analysis of colon adenocarcinoma patients revealed that low levels of miR-205-5p are associated with an unfavorable prognostic compared to those with increased expression, demonstrating the possible clinical utility of miR-205-5p replacement. Exogenous administration of miRNA mimics was not associated with significant changes in cell viability or inflammatory pathways. Therefore, the proposed strategy is aiming towards inhibition of metastasis and limitation of the tumor borders in advanced stages patients in order to prolong the survival time and to increase the efficiency of the current therapeutic strategies.

摘要

EMT 代表结直肠癌晚期的主要程序,在此期间,细胞获得迁移特性,以便侵袭次级组织并形成转移。大多数治疗策略集中于通过不同的凋亡机制减少肿瘤质量,而本研究提倡 miR-205-5p 在损害结肠癌细胞迁移和恢复上皮表型方面的重要作用。在确定结直肠腺癌患者中 miR-205-5p 呈均匀下调图谱后,功能研究表明,通过直接抑制 ZEB1,实验上调该序列能够显著提高 E-钙粘蛋白的水平。此外,CDH1 表达的升高转化为功能参数,其中细胞失去侵袭和迁移特性,并通过粘附相互作用形成均匀的簇。结直肠腺癌患者的生存分析表明,与表达增加的患者相比,miR-205-5p 水平较低与预后不良相关,表明 miR-205-5p 替代的可能临床应用。外源性给予 miRNA 模拟物与细胞活力或炎症途径的显著变化无关。因此,该策略旨在抑制晚期患者的转移和限制肿瘤边界,以延长生存时间并提高当前治疗策略的效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/e711e304074f/41419_2017_102_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/646cea02d758/41419_2017_102_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/475fdba751c9/41419_2017_102_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/64b2fe61db20/41419_2017_102_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/e5c23bafaf73/41419_2017_102_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/2547e531b136/41419_2017_102_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/c8d3ab220c81/41419_2017_102_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/e711e304074f/41419_2017_102_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/646cea02d758/41419_2017_102_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/475fdba751c9/41419_2017_102_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/64b2fe61db20/41419_2017_102_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/e5c23bafaf73/41419_2017_102_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/2547e531b136/41419_2017_102_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/c8d3ab220c81/41419_2017_102_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc7/5833765/e711e304074f/41419_2017_102_Fig7_HTML.jpg

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