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ADAR2 Regulates Malignant Behaviour of Mesothelioma Cells Independent of RNA-editing Activity.
- Source :
-
Anticancer research [Anticancer Res] 2020 Mar; Vol. 40 (3), pp. 1307-1314. - Publication Year :
- 2020
-
Abstract
- Background/aim: Malignant pleural mesothelioma (MPM) is an intractable cancer, and causes of its malignant transformation are not well known. Adenosine deaminase acting on RNA (ADAR) is an RNA-editing enzyme that converts adenosine into inosine in double-stranded RNAs potentially involved in malignant development.<br />Materials and Methods: To examine the role of ADAR1 and ADAR2 in MPM, small interfering RNAs (siRNAs) against ADAR1 or ADAR2 were used.<br />Results: Transfection of siRNA against ADAR2 suppressed proliferation, motility, and invasiveness of MPM cells expressing both ADAR1 and ADAR2; however, siRNA against ADAR1 did not affect these cellular activities. Overexpression of ADAR2, that was incapable of binding to RNA, suppressed growth, motility, and invasion of MPM cells. However, overexpression of ADAR2 that had no enzyme activity did not alter the malignant properties of MPM cells.<br />Conclusion: Enhancement of the malignant characteristics of cultured MPM cells via ADAR2 was independent of RNA-editing activity.<br /> (Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
- Subjects :
- Adenosine Deaminase biosynthesis
Adenosine Deaminase genetics
Cell Line, Tumor
Cell Movement physiology
Cell Proliferation physiology
Humans
Lung Neoplasms enzymology
Lung Neoplasms pathology
Mesothelioma enzymology
Mesothelioma pathology
Mesothelioma, Malignant
RNA, Small Interfering administration & dosage
RNA, Small Interfering genetics
RNA-Binding Proteins biosynthesis
RNA-Binding Proteins genetics
Transfection
Adenosine Deaminase metabolism
Lung Neoplasms genetics
Lung Neoplasms metabolism
Mesothelioma genetics
Mesothelioma metabolism
RNA Editing
RNA-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1791-7530
- Volume :
- 40
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Anticancer research
- Publication Type :
- Academic Journal
- Accession number :
- 32132027
- Full Text :
- https://doi.org/10.21873/anticanres.14072