p85α is a microRNA target and affects chemosensitivity in pancreatic cancer

Abstract Background We previously identified a correlation between increased expression of the phosphoinositide 3-kinase (PI3K) regulatory subunit p85α and improved survival in human pancreatic ductal adenocarcinoma (PDAC). The purpose of this study was to investigate the impact of changes in p85α e...

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Veröffentlicht in:The Journal of surgical research 2015-06, Vol.196 (2), p.285-293
Hauptverfasser: Toste, Paul A., MD, Li, Luyi, MS, Kadera, Brian E., MD, Nguyen, Andrew H., MD, Tran, Linh M., PhD, Wu, Nanping, PhD, Madnick, David L., BS, Patel, Sanjeet G., MD, Dawson, David W., MD, PhD, Donahue, Timothy R., MD
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Sprache:eng
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Zusammenfassung:Abstract Background We previously identified a correlation between increased expression of the phosphoinositide 3-kinase (PI3K) regulatory subunit p85α and improved survival in human pancreatic ductal adenocarcinoma (PDAC). The purpose of this study was to investigate the impact of changes in p85α expression on response to chemotherapy and the regulation of p85α by microRNA-21 (miR-21). Materials and methods PDAC tumor cells overexpressing p85α were generated by viral transduction, and the effect of p85α overexpression on sensitivity to gemcitabine was tested by MTT assay. Primary human PDAC tumors were stained for p85α and miR-21 via immunohistochemistry and in situ hybridization, respectively. Additionally, PDAC cells were treated with miR-21 mimic, and changes in p85α and phospho-AKT were assessed by Western blot. Finally, a luciferase reporter assay system was used to test direct regulation of p85α by miR-21. Results Higher p85α expression resulted in increased sensitivity to gemcitabine ( P  
ISSN:0022-4804
1095-8673
DOI:10.1016/j.jss.2015.02.071