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Inhibition of p22^phox Suppresses Epithelial Ovarian Cancer Cell Proliferation and Tumorigenesis.

ABSTRACT: The aim of this study was to investigate the biological role and molecular mechanism of p22^phox in epithelial ovarian cancer. Immunohistochemistry was employed to determine the p22^phox expression level in epithelial ovarian cancer tissues. The effects of p22^phox on epithelial ovarian cancer cell proliferation, tumorigenesis, and chemosensitivity were evaluated by CCK-8, EdU assay, colony formation and apoptosis assays in vitro and by mouse experiments in vivo. Immunoprecipitation analyses were utilized to explore the potential mechanisms of p22^phox mediated downstream signaling, and RT-PCR and western blot were used to confirm the relevance. P22^phox expression could be detected in epithelial ovarian cancer tissues and normal fallopian epithelial cells. Silencing p22^phox suppressed epithelial ovarian cancer cell proliferation and colony formation capacity in vitro, and inhibited the tumor growth in nude mice bearing the A2780 xenograft in vivo. Mechanistic investigations showed that p22^phox regulated proteasome ubiquitination and subsequent proteasome-dependent degradation of p53 in A2780 and U87 cells in vitro. Furthermore, knockdown of p22^phox significantly increased the chemosensitivity of A2780 cells to cisplatin or paclitaxel. These results suggested that p22^phox as a pivotal oncogene during epithelial ovarian cancer carcinogenesis and p22^phox inhibition might be a potential therapeutic strategy for epithelial ovarian cancer.

SUBMITTER: Li Q

PROVIDER: S-EPMC8176422 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Epithelial ovarian carcinoma (EOC) is the most common cause of gynecological cancer mortality, and poses a threat to women. MicroRNA‑195 (miR‑195) has been reported to induce apoptosis of human OVCAR‑3 cells by inhibiting the VEGFR2/AKT pathway. However, the role of miR‑195 in EOC remains unknown. A previous study reported that cell division cycle 42 (CDC42) can serve as a target gene of miR‑195 and mediate malignant progression of esophageal squamous cell carcinoma (ESCC). The aim of the present study was to investigate the role of miR‑195 in EOC and the regulation in CDC42/CCND1 pathway. Tissues samples and clinical materials were collected from 78 enrolled patients with EOC to analyze the expression and clinical significance of miR‑195, CDC42 and cyclin D1 (CCND1). Human EOC cell lines OVCA420, OVCAR‑3, A2780 and SKOV3 cell lines were used to assess the expression and function of miR‑195, CDC42 and CCND1 in vitro. Cell proliferation, the cell cycle and apoptosis, as well as the cell migratory and invasive abilities were detected in vitro using BrdU incorporation, colony formation, wound healing and Transwell invasion assays, along with flow cytometry. miR‑195 was downregulated, while CDC42 and CCND1 were upregulated in human EOC tissues and cells, and the aberrant expression of both was associated with increased EOC malignancy. Moreover, miR‑195 expression was negatively correlated with CDC42 and CCND1 expression levels, and negatively regulated these expression levels. Thus, it was suggested that miR‑195 functions as a tumor suppressor, but CDC42 and CCND1 act as tumor promoters based their abilities to enhance cell proliferation, cell cycle entry, migration and invasion, as well as decrease apoptosis in OVCAR‑3 cells. the present results demonstrated that miR‑195 inhibited human EOC progression by downregulating CDC42 and CCND1 expression. Furthermore, it was identified that miR‑195, CDC42 and CCND1 may be effective biomarkers for EOC diagnosis and treatment.

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Inhibition of p22^phox Suppresses Epithelial Ovarian Cancer Cell Proliferation and Tumorigenesis.

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Dataset Information

Inhibition of p22phox Suppresses Epithelial Ovarian Cancer Cell Proliferation and Tumorigenesis.

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OmicsDI is part of the ELIXIR infrastructure

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Inhibition of p22^phox Suppresses Epithelial Ovarian Cancer Cell Proliferation and Tumorigenesis.