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Downregulation of long non-coding RNA LINC00460 inhibits the proliferation, migration and invasion, and promotes apoptosis of pancreatic cancer cells via modulation of the miR-320b/ARF1 axis.
- Source :
-
Bioengineered [Bioengineered] 2021 Dec; Vol. 12 (1), pp. 96-107. - Publication Year :
- 2021
-
Abstract
- Pancreatic adenocarcinoma (PAAD) ranks among the most lethal cancers worldwide with high mortality. A marked increase in the level of long non-coding RNA LINC00460 was reported in PAAD patients, in comparison with the healthy controls. However, the underlying mechanisms of the above phenomenon are not yet well understood. Hence, the present study was designed to investigate the molecular mechanism underlying the role of LINC00460 in proliferation, migration and invasion of pancreatic cancer (PC) cells. It was found in our study that LINC00460 knockdown inhibited SW1990 cell proliferation, migration and invasion and promoted its apoptosis. Moreover, miR-320b was targeted straight and its expression was downregulated by LINC00460, whose knockdown led to a reduction in ARF1 expression. Interestingly, miR-320b downregulation partly reversed the effect of LINC00460 knockdown on the proliferation, migration, invasion and apoptosis of SW1990 cells, as well as ARF1expression. In conclusion, LINC00460 knockdown inhibited the proliferation, migration and invasion, and promotes the apoptosis of SW1990 cells via modulation of the miR-320b/ARF1 axis. Thus, LINC00460 can be perceived as a promising target in the treatment of PAAD.
- Subjects :
- ADP-Ribosylation Factor 1 metabolism
Adenocarcinoma genetics
Adenocarcinoma metabolism
Adenocarcinoma pathology
Apoptosis genetics
Cell Line, Tumor
Cell Movement genetics
Cell Proliferation genetics
Humans
MicroRNAs metabolism
RNA, Long Noncoding metabolism
ADP-Ribosylation Factor 1 genetics
Down-Regulation genetics
MicroRNAs genetics
Pancreatic Neoplasms genetics
Pancreatic Neoplasms metabolism
Pancreatic Neoplasms pathology
RNA, Long Noncoding genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2165-5987
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Bioengineered
- Publication Type :
- Academic Journal
- Accession number :
- 33345740
- Full Text :
- https://doi.org/10.1080/21655979.2020.1863035