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MicroRNA-421 promotes proliferation and invasion of non-small cell lung cancer cells through targeting PDCD4.
- Source :
-
Pathology, research and practice [Pathol Res Pract] 2019 Oct; Vol. 215 (10), pp. 152555. Date of Electronic Publication: 2019 Jul 23. - Publication Year :
- 2019
-
Abstract
- Recent evidence highlights that microRNAs serve as crucial regulators of tumorigenesis, including non-small cell lung cancer (NSCLC). The present study was designed to investigate the expression profile, clinical significance and biological role of miR-421 in NSCLC. The results showed that miR-421 expression was markedly increased in NSCLC tissues and cell lines. Further experimental data indicated that knockdown of miR-421 significantly inhibited NSCLC cell proliferation and induced cell cycle arrest in vitro. The migratory and invasive abilities of NSCLC cells were also attenuated following miR-421 knockdown. Furthermore, PDCD4 was identified as a direct target of miR-421, and its expression was inversely correlated with miR-421 expression in NSCLC tissues. PDCD4 also abrogated the oncogenic role of miR-421 in NSCLC cells. Collectively, our study revealed that miR-421 is significantly upregulated in NSCLC and might represent a potential therapeutic target for NSCLC patients.<br /> (Copyright © 2019 Elsevier GmbH. All rights reserved.)
- Subjects :
- Aged
Carcinoma, Non-Small-Cell Lung genetics
Carcinoma, Non-Small-Cell Lung pathology
Cell Line, Tumor
Female
Humans
Lung pathology
Lung Neoplasms genetics
Lung Neoplasms pathology
Male
MicroRNAs genetics
Middle Aged
Neoplasm Invasiveness genetics
Apoptosis Regulatory Proteins metabolism
Carcinoma, Non-Small-Cell Lung metabolism
Cell Proliferation physiology
Lung metabolism
Lung Neoplasms metabolism
MicroRNAs metabolism
Neoplasm Invasiveness pathology
RNA-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1618-0631
- Volume :
- 215
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Pathology, research and practice
- Publication Type :
- Academic Journal
- Accession number :
- 31445715
- Full Text :
- https://doi.org/10.1016/j.prp.2019.152555