Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/10110
Title: | Downregulation of VANGL1 inhibits cellular invasion rather than cell motility in hepatocellular carcinoma cells without stimulation | Authors: | Çetin, Gökhan Ozan Toylu, Aslı Atabey, Neşe Sercan, Zeynep Sakızlı, Meral |
Keywords: | messenger RNA protein VANGL1 small interfering RNA unclassified drug Wnt protein carrier protein membrane protein VANGL1 protein, human Article cancer growth cell fate cell invasion cell motility cell polarity cell proliferation controlled study down regulation gene gene expression gene silencing genetic transfection HepG2 cell line human human cell liver cell carcinoma VANGL1 gene antagonists and inhibitors biosynthesis cell motion genetics Hep-G2 cell line liver tumor metabolism pathology physiology signal transduction tumor cell line tumor invasion Wnt signaling pathway Carcinoma, Hepatocellular Carrier Proteins Cell Line, Tumor Cell Movement Down-Regulation Gene Expression Hep G2 Cells Humans Liver Neoplasms Membrane Proteins Neoplasm Invasiveness RNA, Small Interfering Signal Transduction Transfection Wnt Signaling Pathway |
Publisher: | Mary Ann Liebert Inc. | Abstract: | Aims: The Wnt planar cell polarity (PCP) pathway is one of the Wnt pathways which plays a critical role in cell proliferation and fate. The VANGL1 protein is one of Wnt-PCP pathway components. It is known that Wnt-PCP pathway has major roles in cell motility but its role in hepatocellular carcinoma (HCC) progression through invasion and metastasis needs to be clarified. Methods: We silenced VANGL1 gene expression in the HepG2 HCC cell line by stable transfection with a vector containing siRNA template for VANGL1 and investigated the change in cell invasion and motility. Results: Transfected cells with the siRNA template showed significantly suppressed invasive capacity when compared to controls although cellular motility was only slightly affected. Conclusion: Our study showed a basal role for VANGL1 with respect to the invasive capacity of HCC cells. This suggests that the Wnt-PCP pathway may play a role in progression of HCC through cellular invasion but further studies are needed to clarify its role in cell motility. © 2015, Mary Ann Liebert, Inc. | URI: | https://hdl.handle.net/11499/10110 https://doi.org/10.1089/gtmb.2015.0014 |
ISSN: | 1945-0265 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
Files in This Item:
File | Size | Format | |
---|---|---|---|
Gökhan Ozan Çetin.pdf | 160.31 kB | Adobe PDF | View/Open |
CORE Recommender
SCOPUSTM
Citations
9
checked on Dec 21, 2024
WEB OF SCIENCETM
Citations
9
checked on Dec 19, 2024
Page view(s)
42
checked on Aug 24, 2024
Download(s)
16
checked on Aug 24, 2024
Google ScholarTM
Check
Altmetric
Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.