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

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