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Suppression of EIF4G2 by miR-379 potentiates the cisplatin chemosensitivity in nonsmall cell lung cancer cells.
- Source :
-
FEBS letters [FEBS Lett] 2017 Feb; Vol. 591 (4), pp. 636-645. Date of Electronic Publication: 2017 Feb 20. - Publication Year :
- 2017
-
Abstract
- Although microRNAs and EIF4G2 are both known to play pivotal roles in cancer progression, it remains unknown whether these pathways regulate chemosensitivity in a coordinated manner. Here, we show that miR-379 expression is significantly downregulated in chemoresistant nonsmall cell lung cancer (NSCLC) tissues and cells. Manipulation of miR-379 levels could alter the in vitro and in vivo cisplatin (CDDP) resistance in lung cancer (LCa) cells. Mechanistically, miR-379 potentiated LCa chemosensitivity via modulation of CDDP-induced apoptosis by directly targeting the EIF4G2 3'UTR. Additionally, we observed an inverse correlation between miR-379 and EIF4G2 expression in LCa tissues from patients with CDDP-based chemotherapy. Together, our findings shed new light on the potential involvement of miR-379/EIF4G2 cascade in the pathogenesis of CDDP resistance in LCa.<br /> (© 2017 Federation of European Biochemical Societies.)
- Subjects :
- 3' Untranslated Regions genetics
A549 Cells
Animals
Antineoplastic Agents pharmacology
Apoptosis drug effects
Apoptosis genetics
Base Sequence
Carcinoma, Non-Small-Cell Lung genetics
Carcinoma, Non-Small-Cell Lung metabolism
Cell Line
Cell Line, Tumor
Eukaryotic Initiation Factor-4G metabolism
Gene Expression Regulation, Neoplastic
HEK293 Cells
Humans
Immunoblotting
Lung Neoplasms genetics
Lung Neoplasms metabolism
Mice, Nude
Reverse Transcriptase Polymerase Chain Reaction
Sequence Homology, Amino Acid
Xenograft Model Antitumor Assays
Carcinoma, Non-Small-Cell Lung drug therapy
Cisplatin pharmacology
Eukaryotic Initiation Factor-4G genetics
Lung Neoplasms drug therapy
MicroRNAs genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3468
- Volume :
- 591
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 28117895
- Full Text :
- https://doi.org/10.1002/1873-3468.12566