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ADGRF4 Regulates Non-small Cell Lung Cancer Cell Invasiveness.
- Source :
-
Anticancer research [Anticancer Res] 2020 Dec; Vol. 40 (12), pp. 6835-6844. - Publication Year :
- 2020
-
Abstract
- Background/aim: Adhesion G protein-coupled receptors (aGPCRs) have a crucial role in cancer. However, the role of ADGRF4, one of aGPCRs, in cancer has yet to be revealed. Therefore, we investigated its role in lung cancer, a leading cause of cancer-related deaths worldwide.<br />Materials and Methods: ADGRF4 gene expression pattern in lung cancer were analyzed by in silico analyses. RNA sequencing was conducted to investigate gene expression pattern altered by ADGRF4 knockdown. Lung cancer cell lines were subjected to cell migration and invasion assays.<br />Results: In silico analysis data indicated a major role of ADGRF4 in lung cancer. RNA sequencing data showed that ADGRF4 gene silencing in lung cancer cells altered global expression pattern. ADGRF4 gene silencing reduced lung cancer cell invasiveness. Furthermore, PPP2C gene expression was most significantly down-regulated by ADGRF4 gene silencing. PPP2C overexpression rescued cell invasiveness inhibited by ADGRF4 gene silencing, and PPP2C gene silencing blocked lung cancer cell invasiveness.<br />Conclusion: ADGRF4 regulates lung cancer cell invasiveness via PPP2C.<br /> (Copyright © 2020 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
- Subjects :
- Biomarkers, Tumor
Carcinoma, Non-Small-Cell Lung mortality
Cell Line, Tumor
Gene Expression Regulation, Neoplastic
Gene Knockdown Techniques
Humans
Lung Neoplasms mortality
Neoplasm Invasiveness
Neoplasm Staging
Prognosis
Receptors, G-Protein-Coupled metabolism
Carcinoma, Non-Small-Cell Lung genetics
Carcinoma, Non-Small-Cell Lung pathology
Lung Neoplasms genetics
Lung Neoplasms pathology
Receptors, G-Protein-Coupled genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1791-7530
- Volume :
- 40
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Anticancer research
- Publication Type :
- Academic Journal
- Accession number :
- 33288575
- Full Text :
- https://doi.org/10.21873/anticanres.14705