| Literature DB >> 30109500 |
Maria Luisa Gasparri1,2,3, Zein Mersini Besharat4, Ammad Ahmad Farooqi5, Sumbul Khalid6, Katayoun Taghavi7, Raad Aris Besharat8, Claudia Sabato9,10, Andrea Papadia7, Pierluigi Benedetti Panici8, Michael David Mueller7, Elisabetta Ferretti4,11.
Abstract
Ovarian cancer is a leading cause of death among gynecologic malignancies. This disappointing prognosis is closely related to intrinsic or acquired resistance to conventional platinum-based chemotherapy, which can affect a third of patients. As such, investigating relevant molecular targets is crucial in the fight against this disease. So far, many mutations involved in ovarian cancer pathogenesis have been identified. Among them, a few pathways were implicated. One such pathway is the P13K/AKT/mTOR with abnormalities found in many cases. This pathway is considered to have an instrumental role in proliferation, migration, invasion and, more recently, in chemotherapy resistance. Many miRNAs have been found to influence P13K/AKT/mTOR pathway with different potential role in tumor genesis and ovarian cancer behaviour. In particular, their biological function was recently investigated as regards chemoresistance, therefore, leading to the identification of potential specific indirect biomarker of platinum sensitivity in ovarian cancer.Entities:
Keywords: MicroRNA; Ovarian cancer; PI3K/AKT/mTOR pathway; Platinum resistance
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Year: 2018 PMID: 30109500 DOI: 10.1007/s00432-018-2737-y
Source DB: PubMed Journal: J Cancer Res Clin Oncol ISSN: 0171-5216 Impact factor: 4.553