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PMID: 27906681 Published · ppublish English Journal Article

siRNA-mediated suppression of collagen type iv alpha 2 (COL4A2) mRNA inhibits triple-negative breast cancer cell proliferation and migration.

Oncotarget ·Vol. 8 ·No. 2 ·2017-01-10 ·Pages 2585-2593

JingSong H, Hong G, Yang J, Duo Z, Li F, WeiCai C, XueYing L, YouSheng M, YiWen O, Yue P, Zou C

Abstract

Triple-negative breast cancer (TNBC) is more aggressive than other breast cancer subtypes. Collagen type IV alpha 2 (COL4A2), a major component of the basement membrane, dynamically influences a wide range of biological processes, including cancer pathogenesis and progression. This study evaluated the effects of COL4A2 siRNA delivered by lentiviral vector to TNBC cells. COL4A2 siRNA lenti-viral vector was constructed and transfected into MDA-MB-231 and MDA-MB-468 cells. The COL4A2 mRNA levels were quantified by RT-PCR. CCK8 assay was performed to evaluate cell proliferation and migration. Cell migration and invasion assays were carried out using Transwell. Cell apoptosis and cell cycle analyses were conducted using flow cytometric approach. We found that COL4A2 mRNA levels were significantly down-regulated in MDA-MB-231 and MDA-MB-468 cells after transfection with COL4A2 siRNA. Furthermore, cell migration and proliferation were significantly decreased and the cell cycle was arrested. Our results indicated that COL4A2 siRNA significantly suppresses the migration and proliferation of TNBC cells. Inhibition of COL4A2 may be a new target for the prevention and treatment of TNBC.

Keywords
COL4A2 lentiviral vector small interfering RNA (siRNA) triple-negative breast cancer (TNBC)
MeSH Terms
Apoptosis Cell Line, Tumor Cell Movement Cell Proliferation Collagen Type IV/genetics Female Gene Expression Regulation, Neoplastic Gene Silencing Humans RNA, Small Interfering/pharmacology Triple Negative Breast Neoplasms/genetics Up-Regulation
Chemicals
COL4A2 protein, human Collagen Type IV RNA, Small Interfering
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
JingSong He
Department of Breast Surgery, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen, 518035, China.
Hong Guan
Department of Pathology, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen 518035, China.
Yang Jianbo
Department of Laboratory Medicine and Pathology, Masonic Cancer Center, University of Minnesota, UMN Twin Cities, MN 55455, USA.
Duo Zheng
Shenzhen Key Laboratory of Translational Medicine of Tumor, Department of Cell Biology and Genetics, School of Medicine, Shenzhen University, Shenzhen, Guangdong, 518060, China.
Li Fu
Department of Pharmacology, Shenzhen Key Laboratory of Translational Medicine of Tumor and Cancer Research Centre, School of Medicine, Shenzhen University, Shenzhen, 518060 China.
WeiCai Chen
Department of Breast Surgery, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen, 518035, China.
XueYing Luo
Department of Breast Surgery, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen, 518035, China.
YouSheng Mao
Department of Breast Surgery, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen, 518035, China.
YiWen OuYang
Department of Breast Surgery, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen, 518035, China.
Yue Pan
Department of Breast Surgery, The First Affiliated Hospital of Shenzhen University, Second People's Hospital of Shen Zhen, Shen Zhen, 518035, China.
Zou Chang
Clinical Medical Research Center, Shen Zhen People's Hospital, The Second Clinical Medical College of Jinan University, 518020, China.
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Article Info
Journal
Oncotarget
Abbr.
Oncotarget
ISSN
1949-2553
Published
2017-01-10
Pages
2585-2593
Language
English
Region
United States
NLM ID
101532965
PMCID
PMC5356825
Subset
IM
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