miR-191 Modulates Malignant Transformation of Endometriosis Through Regulating TIMP3

Source of support: Departmental sources Background: Although aberrant expression of several miRNAs was found during the pathological development of endome-triosis to endometriosis-associated ovarian cancer (EAOC), their roles are not fully understood. miR-191 is a miRNA significantly upregulated in endometriosis and EAOC patients. However, its downstream network is still not clear. This study explored its role in malignant transformation of endometriosis to EAOC. Material/Methods: Tissues from 12 healthy controls, 12 patients with endometriomas, and 12 patients with EAOC were used to verify miR-191 expression by using qRT-PCR. Endometriosis cell line CRL-7566 and ovarian endometrioid car-cinoma cell line CRL-11731 were used to explore the downstream regulative function of miR-191. Results: By using tissue and serum samples from healthy, endometriosis, and EAOC participants, we confirmed that miR-191 expression was significantly higher in endometriosis and EAOC participants. Interestingly, we also ob-served that TIMP3 expression was negatively correlated with miR-191 expression. Overexpressing miR-191 in CRL-7566 significantly increased cell proliferation and invasion, while miR-191 knockdown in CRL-11731 cells significantly decreased cell proliferation and invasion. These modulating effects of miR-191 are achieved through its regulation of TIMP3. Conclusions: miR-191 can directly regulate TIMP3 expression, thereby affecting cell proliferation rate and invasion ability.