
pmid: 27600258
As few prognostic markers and symptoms have been identified, ovarian cancer is typically diagnosed at an advanced stage, and a majority of patients will relapse and develop resistance to anticancer drugs such as paclitaxel. Musashi-2 (MSI2) is a regulator of gene translation and functions as an oncogenic protein and a marker of poor prognosis in various types of cancer. However, the biological and clinical significance of MSI2 in ovarian cancer remains unclear. Using a tissue microarray-based assay, we demonstrated that MSI2 was highly expressed in advanced, serous ovarian cancer tissues. In addition, MSI2-overexpressing ovarian cancer cells exhibited increased viability, proliferation and growth. We found that MSI2 was overexpressed in paclitaxel-resistant ovarian cancer SKOV3-TR cells but not in paclitaxel-sensitive cell lines. The loss of MSI2 expression in lentivirus-mediated stable MSI2 knockdown SKOV3-TR cells impaired paclitaxel resistance as determined using cell viability and apoptosis assays. In contrast, lentivirus-mediated MSI2 overexpression promoted the development of paclitaxel resistance in paclitaxel-sensitive ovarian cancer cells. The results of the present study are the first to demonstrate that MSI2 is a valuable marker of advanced, serous ovarian cancer and that MSI2 plays an important role in paclitaxel resistance.
Ovarian Neoplasms, Paclitaxel, Blotting, Western, Apoptosis, Prognosis, Adenocarcinoma, Mucinous, Antineoplastic Agents, Phytogenic, Cystadenocarcinoma, Serous, Endometrial Neoplasms, Gene Expression Regulation, Neoplastic, Immunoenzyme Techniques, Drug Resistance, Neoplasm, Biomarkers, Tumor, Humans, Female, RNA, Messenger, Neoplasm Recurrence, Local, Adenocarcinoma, Clear Cell, Cell Proliferation, Neoplasm Staging
Ovarian Neoplasms, Paclitaxel, Blotting, Western, Apoptosis, Prognosis, Adenocarcinoma, Mucinous, Antineoplastic Agents, Phytogenic, Cystadenocarcinoma, Serous, Endometrial Neoplasms, Gene Expression Regulation, Neoplastic, Immunoenzyme Techniques, Drug Resistance, Neoplasm, Biomarkers, Tumor, Humans, Female, RNA, Messenger, Neoplasm Recurrence, Local, Adenocarcinoma, Clear Cell, Cell Proliferation, Neoplasm Staging
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