MicroRNA-130a-3p impedes the progression of papillary thyroid carcinoma through downregulation of KPNB1 by targeting PSME3

• Published in: Endocrine 2023-10, Vol.82 (1), p.96-107
• Main Authors: Wang, Yan, Xu, Jinmei, Zhu, Xiaodan, Kuang, Hongyu
• Format: Article
• Language: English
• Subjects: Apoptosis; Cell growth; Cell migration; Cell proliferation; Cholecystokinin; Diabetes; E-cadherin; Endocrinology; Flow cytometry; Humanities and Social Sciences; Immunoprecipitation; Internal Medicine; Malignancy; Medical prognosis; Medicine; Medicine & Public Health; MicroRNAs; miRNA; multidisciplinary; N-Cadherin; Original Article; Papillary thyroid carcinoma; Proliferating cell nuclear antigen; Science; Thyroid cancer; Transfection; Tumors; Western blotting
• ISSN: 1559-0100; 1355-008X; 1559-0100
• DOI: 10.1007/s12020-023-03383-x

Background: Papillary thyroid carcinoma (PTC) is the main type of thyroid cancer (THCA). Despite the good prognosis, some PTC patients may deteriorate into more aggressive disease, leading to poor survival. Our study aimed to explore the role of microRNA (miR)-130a-3p in regulating PTC. Methods: After transfection with miR-130a-3p -mimic, OE- PSME3 , or miR-130a-3p -mimic + OE- KPNB1 in PTC cells (TPC-1), CCK-8, Transwell, scratch, and flow cytometry experiments were performed to analyze TPC-1 cell proliferation, invasion, migration, and apoptosis. Western blotting was used to detect proliferation or invasion-related protein markers ( PCNA , E-cadherin , and N-cadherin ). The RNA22 database, dual-luciferase reporter assay, and RNA pull-down assay were applied for the prediction and verification of the binding site between miR-130a-3p and PSME3 . Pan-cancer software identified a positive correlation between PSME3 and KPNB1 in THCA. Co-immunoprecipitation was utilized to verify the interaction of PSME3 with KPNB1 . Nude mice were transplanted with TPC-1 cells overexpressing miR-130a-3p . The tumors were isolated for detection of the expression of miR-130a-3p , PSME3 , KPNB1 , Ki-67 , and CD31 . Results: miR-130a-3p was lowly expressed in PTC cell lines. Upregulation of miR-130a-3p repressed the expression of PSME3 and KPNB1 and reduced the malignancy of TPC-1 cells in vitro, shown by inhibited cell proliferation, invasion, migration, and the expression of PCNA and N-cadherin . Also, overexpressed miR-130a-3p inhibited the growth of xenograft tumors in nude mice. miR-130a-3p bound to PSME3 which interacted with KPNB1 . Conclusion: miR-130a-3p impedes the progression of PTC by downregulating PSME3 / KPNB1 .