دورية أكاديمية

MicroRNA-27a Promotes the Proliferation and Invasiveness of Colon Cancer Cells by Targeting SFRP1 through the Wnt/β-Catenin Signaling Pathway

التفاصيل البيبلوغرافية
العنوان: MicroRNA-27a Promotes the Proliferation and Invasiveness of Colon Cancer Cells by Targeting SFRP1 through the Wnt/β-Catenin Signaling Pathway
المؤلفون: Sang Ba, Yi Xuan, Zi-Wen Long, Hai-Yong Chen, Shu-Sen Zheng
المصدر: Cellular Physiology and Biochemistry, Vol 42, Iss 5, Pp 1920-1933 (2017)
بيانات النشر: Cell Physiol Biochem Press GmbH & Co KG, 2017.
سنة النشر: 2017
المجموعة: LCC:Physiology
LCC:Biochemistry
مصطلحات موضوعية: Colon cancer, MicroRNA-27a, Secreted Frizzled-related protein 1, Wnt/β-catenin signaling pathway, Proliferation, Invasion, Physiology, QP1-981, Biochemistry, QD415-436
الوصف: Objective: This study aims to explore the effects of microRNA-27a (miR-27a) on the proliferation and invasiveness of colon cancer cells through the Secreted Frizzled-related protein 1 (SFRP1) and the Wnt/β-catenin signaling pathway. Methods: Colon cancer tissues and adjacent normal tissues from 125 colon cancer patients, together with the HCEpic, HCT-116, HT-29, SW480 and SW620 cell lines, were prepared for this study. The transfected HCT-116 cells were divided into the miR-27a mimics, miR-27a-NC, anti-miR-27a, blank, Lv-SFRP1, Lv-NC, and miR-27a mimics + Lv-SFRP1 groups. RT-qPCR was performed to detect the expressions of miR-27a and SFRP1 mRNA. A dual-luciferase reporter assay was conducted to examine the effect of miR-27a on SFRP1. Western blotting was used to measure the expressions of the SFRP1, β-catenin, GSK-3β, p-β-catenin, p-GSK-3β, c-Myc and cyclin D1 proteins. MTT, soft agar clone formation and Transwell chamber assays were performed to detect cell proliferation and invasion. Results: Compared with normal tissues and cells, colon cancer tissues and cells demonstrated significantly higher expression of miR-27a, but lower expressions of SFRP1 mRNA and protein. MiR-27a negatively regulated the expression of SFRP1 mRNA. SFRP1 was also found to be a target gene of miR-27a. In the miR-27a mimic group, the proliferation and invasiveness of colon cancer cells were significantly increased, while the expressions of GSK-3 β and p-β-catenin were remarkably down-regulated; in contrast, the expressions of p-GSK-3β, -catenin, c-Myc and cyclin D1 were up-regulated. While the proliferation and invasiveness of colon cancer cells in the anti-miR-27a and Lv-SFRP1 groups were decreased, the expressions of GSK-3β and p-β-catenin were elevated, and the expressions of p-GSK-3β, β-catenin, c-Myc and cyclin D1 were decreased. Conclusion: These findings indicated that miR-27a could promote the proliferation and invasiveness of colon cancer cells by targeting SFRP1 through the Wnt/β-catenin signaling pathway.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1015-8987
1421-9778
00047961
العلاقة: http://www.karger.com/Article/FullText/479610Test; https://doaj.org/toc/1015-8987Test; https://doaj.org/toc/1421-9778Test
DOI: 10.1159/000479610
الوصول الحر: https://doaj.org/article/8c26b43b977040af982668fc35eeb77bTest
رقم الانضمام: edsdoj.8c26b43b977040af982668fc35eeb77b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10158987
14219778
00047961
DOI:10.1159/000479610