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Involvement of microRNA-93, a new regulator of PTEN/Akt signaling pathway, in regulation of chemotherapeutic drug cisplatin chemosensitivity in ovarian cancer cells
► MiR-93 is significantly up-regulated in cisplatin-resistant ovarian cancer cells. ► MiR-93 regulates cisplatin sensitivity through directly targeting PTEN. ► MiR-93 exhibits opposite alteration tendency to PTEN in ovarian cancer tissues. ► MiR-93 as a new regulator of PTEN participated in the PTEN...
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Published in: | FEBS letters 2012-05, Vol.586 (9), p.1279-1286 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► MiR-93 is significantly up-regulated in cisplatin-resistant ovarian cancer cells. ► MiR-93 regulates cisplatin sensitivity through directly targeting PTEN. ► MiR-93 exhibits opposite alteration tendency to PTEN in ovarian cancer tissues. ► MiR-93 as a new regulator of PTEN participated in the PTEN/AKT signaling pathway.
The mechanisms underlying ovarian cancer cell resistance to cisplatin (CDDP) are not fully understood. MicroRNAs (miRNAs) play important roles in tumorigenesis and drug resistance. In this paper, we utilized microRNA array and real-time PCR to show that miR-93 is significantly up-regulated in cisplatin-resistant ovarian cancer cells. In vitro assays show that over-expression and knock-down of miR-93 regulate apoptotic activity, and thereby cisplatin chemosensitivity, in ovarian cells. Furthermore, we found that miR-93 can directly target PTEN, and participates in the regulation of the AKT signaling pathway. MiR-93 inversely correlates with PTEN expression in CDDP-resistant and sensitive human ovarian cancer tissues. These results may have implications for therapeutic strategies aiming to overcome ovarian cancer cell resistance to cisplatin. |
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ISSN: | 0014-5793 1873-3468 |
DOI: | 10.1016/j.febslet.2012.03.006 |