RRC ID 55971
Author Kurata A, Yamada M, Ohno SI, Inoue S, Hashimoto H, Fujita K, Takanashi M, Kuroda M.
Title Expression level of microRNA-200c is associated with cell morphology in vitro and histological differentiation through regulation of ZEB1/2 and E-cadherin in gastric carcinoma.
Journal Oncol. Rep.
Abstract Scirrhous type gastric cancer is characterized by diffuse infiltration of poorly differentiated adenocarcinoma cells and poor prognosis. Although association of poorly differentiated histology with reduction in E-cadherin expression, as well as association of microRNA (miR)-200c with E-cadherin through regulation of ZEB1/2, has been reported, participation of miR-200c in gastric carcinogenesis is not fully understood. We used 6 cell lines originating from gastric cancers, and investigated levels of miR-200c along with its target mRNAs ZEB1/2 and E-cadherin by qRT-PCR. ZEB1 and E-cadherin protein expression was also assessed via western blotting. Furthermore, we investigated the expression levels of miR‑200c by in situ hybridization, along with the expression of ZEB1 and E-cadherin by immunohistochemistry, in 97 gastric adenocarcinoma tissues. Inverse correlation between miR‑200c and ZEB1 levels were obtained by qRT-PCR in cell lines (P<0.05). Cell lines with low miR-200c and high ZEB1 exhibited low E-cadherin expression in both qRT-PCR and western blotting, and exhibited spindle-shaped morphology, in contrast to round cell morphology in those cell lines with high miR-200c levels. Inverse correlations were also obtained between miR-200c and ZEB1 as well as between ZEB1 and E-cadherin levels in tissue samples (P<0.001). Cancer tissues with low miR-200c, high ZEB1, and low E-cadherin expression were associated with poorly differentiated histology, in contrast to tubular form in cancers with high miR-200c expression levels (P<0.001). Our data revealed that downregulation of miR-200c primarily regulated cell morphology by downregulation of E-cadherin through upregulation of ZEB1, leading to poorly differentiated histology in gastric cancer.
Volume 39(1)
Pages 91-100
Published 2018-1
DOI 10.3892/or.2017.6093
PMID 29138864
PMC PMC5783608
MeSH Adenocarcinoma, Scirrhous / genetics Adenocarcinoma, Scirrhous / metabolism Adenocarcinoma, Scirrhous / pathology* Adult Aged Aged, 80 and over Antigens, CD Cadherins / genetics Cadherins / metabolism* Cell Differentiation Cell Line, Tumor Epithelial-Mesenchymal Transition Female Gene Expression Regulation, Neoplastic Humans In Vitro Techniques Male MicroRNAs / genetics* Middle Aged Stomach Neoplasms / genetics Stomach Neoplasms / metabolism Stomach Neoplasms / pathology* Tumor Burden Zinc Finger E-box Binding Homeobox 2 / genetics Zinc Finger E-box Binding Homeobox 2 / metabolism* Zinc Finger E-box-Binding Homeobox 1 / genetics Zinc Finger E-box-Binding Homeobox 1 / metabolism*
Resource
Human and Animal Cells H-111-TC(RCB1884) HGC-27(RCB0500) Kato III(RCB2088) MKN1(RCB1003) MKN45(RCB1001) NUGC-4RCB1939)