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KMID : 0381120220440091091
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Genes and Genomics
2022 Volume.44 No. 9 p.1091 ~ p.1097
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Effect of human endogenous retrovirus-K env gene knockout on proliferation of ovarian cancer cells
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Ko Eun-Ji
Kim Eun-Taeg
Kim Heung-Yeol
Lee Chul-Min
Koh Suk-Bong
Eo Wan-Kyu
Kim Hong-Bae
Oh Young-Lim
Ock Mee-Sun
Kim Ki-Hyung
Cha Hee-Jae
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Abstract
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Background: Among various human endogenous retroviruses (HERVs), the HERV-K (HML-2) group has been reported to be highly related to cancer. In pancreatic cancer cells, shRNA-mediated downregulation of HERV-K env RNA decreases cell proliferation and tumor growth through the RAS-ERK-RSK pathway; in colorectal cancer, CRISPR-Cas9 knockout (KO) of the HERV-K env gene affects tumorigenic characteristics through the nupr-1 gene.
Objective: The effect of HERV-K env KO has not been studied in ovarian cancer cell lines. In this study, we analyzed the tumorigenic characteristics of ovarian cancer cell lines, including cell proliferation, migration, and invasion, and the expression patterns of related proteins after CRISPR-Cas9 KO of the HERV-K env gene.
Methods: The HERV-K env gene KO was achieved using the CRISPR-Cas9 system in ovarian cancer cell lines SKOV3 and OVCAR3. Tumorigenic characteristics including cell proliferation, migration, and invasion were analyzed, and related protein expression was investigated by western blot analysis.
Results: The expression of the HERV-K env gene in KO cells was significantly reduced at RNA and protein levels, and tumorigenic characteristics including cell proliferation, migration, and invasion were significantly reduced. In HERV-K env KO SKOV3 cells, the expression of the RB protein was significantly up-regulated and the cyclin B1 protein level was significantly reduced. In contrast, in HERV-K env KO OVCAR3 cells, the level of phospho-RB protein was significantly reduced, but other protein levels were not changed.
Conclusion: The results of this study showed that HERV-K env gene KO affects cell proliferation, invasion, and migration of ovarian cells through RB and Cyclin B1 proteins, but the specific regulation pattern can differ by cell line.
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KEYWORD
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HERV-K env, Cell proliferation, CRISPR-Cas9, RB, Cyclin B1, Tumor suppressor, Ovarian cancer, Invasion, Migration
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