Abstract
Ovarian cancer has a high mortality with low five-year survival rates. The role of the E3 ligase Makorin ring finger protein 2 (MKRN2) in ovarian cancer is unknown. This study investigated the impact of MKRN2 on the growth of ovarian cancer. MKRN2 expression in ovarian cancer tissue was analyzed by immunohistochemistry. Overexpression of MKRN2 was induced in two ovarian cancer cell lines (SKOV3 and CAOV3) by lentivirus transfection, and expression levels were verified by western blotting. Proliferation and growth were determined by CCK-8 and colony formation assays, while migration was examined using transwell assays and apoptosis by flow cytometry. Xenograft tumors of transfected SKOV3 cells were established in mice, and immunohistochemistry and TUNEL assays measured MKRN2 levels and apoptosis in tumor cells. Reduced levels of MKRN2 in cancerous tissue relative to non-cancerous ovarian tissues. Lentiviral-based MKRN2 overexpression in SKOV3 and CAOV3 cells reduced tumor-associated behavior while inducing apoptosis in vitro. In xenograft tumors, MKRN2 overexpression inhibited ovarian cancer growth and increased apoptosis in vivo. These findings imply the MKRN2 involvement in ovarian carcinogenesis and suggest its potential for treating the disease.
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The text was submitted by the author(s) in English.
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The study is funded by the National Natural Science Foundation of China (no. 81302251) and the Suzhou Science and Education Project for Youth scholars (JKXW2018078).
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Feizhou Jiang and Qinjian Xia have contributed equally to this work. Feizhou Jiang and Qinjian Xia designed the study, conducted experimental studies, and completed the manuscript. Lei Wu participated in the experimental studies and data analysis. Yueming Zhang supervised the work and reviewed the manuscript. All authors read and approved the final manuscript.
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Jiang, F.Z., Xia, Q.J., Wu, L. et al. Overexpression of MKRN2 Inhibits the Growth of Ovarian Cancer Cells. Mol Biol 57, 684–691 (2023). https://doi.org/10.1134/S002689332304009X
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DOI: https://doi.org/10.1134/S002689332304009X