USP18 contributes to the proliferation and migration of ovarian cancer cells by regulating the AKT/mTOR signaling pathway

Meiqin Liu; Shile Gao; Xingjun Xu; Lijie Zhang; Bin Xu; Donghui Lu

doi:10.18388/abp.2020_5871

USP18 contributes to the proliferation and migration of ovarian cancer cells by regulating the AKT/mTOR signaling pathway

Meiqin Liu Tumor Ward 4, The 901ST Hospital of the Joint Logistics Support Force of PLA, Hefei, Anhui Province, China
Shile Gao Tumor Ward 4, The 901ST Hospital of the Joint Logistics Support Force of PLA, Hefei, Anhui Province, China
Xingjun Xu Tumor Ward 4, The 901ST Hospital of the Joint Logistics Support Force of PLA, Hefei, Anhui Province, China
Lijie Zhang Tumor Ward 4, The 901ST Hospital of the Joint Logistics Support Force of PLA, Hefei, Anhui Province, China
Bin Xu Tumor Ward 4, The 901ST Hospital of the Joint Logistics Support Force of PLA, Hefei, Anhui Province, China
Donghui Lu Tumor Ward 4, The 901ST Hospital of the Joint Logistics Support Force of PLA, Hefei, Anhui Province, China

DOI: https://doi.org/10.18388/abp.2020_5871

Abstract

Ubiquitin-specific peptidase (USP)18 is elevated in tumor tissues and is associated with tumor malignancy. USP18 functions as an oncogene in different cancers. However, the role of USP18 in ovarian cancer was poorly understood. TCGA database showed that USP18 was elevated in ovarian cancer tissues. Additionally, USP18 mRNA and protein expression was also up-regulated in tumor tissues. The functional assays were then designed via siRNA-mediated knockdown of USP18. The results showed that knockdown of USP18 reduced cell viability and ovarian cancer proliferation. Furthermore, cell apoptosis was promoted by USP18 silencing, and interference of USP18 suppressed cell migration and invasion. The expression of phosphorylated AKT (p-AKT) and p-mTOR protein was decreased in ovarian cancer cells by USP18 knockdown. Inhibition of AKT attenuated the decrease in cell apoptosis induced by USP18 overexpression and increased cell viability and migration. In conclusion, USP18 promoted the proliferation and migration of ovarian cancer cells by activating AKT/mTOR signaling.

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Published

2022-06-13

Issue

Vol. 69 No. 2 (2022)

Section

Articles

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