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miR-let-7f-1 regulates SPARC mediated cisplatin resistance in medulloblastoma cells.
- Source :
-
Cellular signalling [Cell Signal] 2014 Oct; Vol. 26 (10), pp. 2193-201. Date of Electronic Publication: 2014 Jul 08. - Publication Year :
- 2014
-
Abstract
- Our previous studies indicate that Secreted Protein Acidic and Rich in Cysteine (SPARC) expression suppressed medulloblastoma tumor growth in vitro and in vivo. Here we sought to determine the effect of SPARC expression in medulloblastoma cells to chemotherapeutic agents. In this study, we show that SPARC expression induces cisplatin resistance in medulloblastoma cells. We also demonstrate that the autophagy was involved in SPARC expression mediated resistance to cisplatin. Suppression of autophagy by either autophagy inhibitor, 3-methyladenosine (3MA) or Atg5 siRNA enhanced cisplatin sensitivity in SPARC expressed cells. Further, SPARC expression suppressed miR-let-7f-1 expression which resulted in disrupted repression of High Mobility Group Box 1 (HMGB1), a critical regulator of autophagy. We also show that HMGB1 is a direct target of miR-let-7f-1 and forced expression of HMGB1 cDNA enhanced cisplatin sensitivity in SPARC expressed cells. In summary, our results suggest that SPARC modulates cisplatin resistance by modulating the Let-7f-1 miRNA/HMGB1 axis in medulloblastoma cells.<br /> (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Subjects :
- Adenosine analogs & derivatives
Adenosine pharmacology
Antineoplastic Agents toxicity
Autophagy drug effects
Autophagy-Related Protein 5
Cell Line, Tumor
Cell Survival drug effects
Cisplatin toxicity
Drug Resistance, Neoplasm
HMGB1 Protein genetics
HMGB1 Protein metabolism
Humans
Medulloblastoma metabolism
Medulloblastoma pathology
MicroRNAs genetics
Microtubule-Associated Proteins antagonists & inhibitors
Microtubule-Associated Proteins genetics
Microtubule-Associated Proteins metabolism
Osteonectin genetics
RNA Interference
RNA, Small Interfering metabolism
MicroRNAs metabolism
Osteonectin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3913
- Volume :
- 26
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Cellular signalling
- Publication Type :
- Academic Journal
- Accession number :
- 25014664
- Full Text :
- https://doi.org/10.1016/j.cellsig.2014.06.014