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PLK1在不同TP53基因型宫颈癌细胞中的作用

孟繁杰 周丽 邢思宁 于卉影

中国医科大学学报2026,Vol.55Issue(8):687-692,6.
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中国医科大学学报2026,Vol.55Issue(8):687-692,6.DOI:10.12007/j.issn.0258-4646.2026.08.003

PLK1在不同TP53基因型宫颈癌细胞中的作用

Effect of PLK1 on cervical cancer cells with different TP53 genotypes

孟繁杰 1周丽 1邢思宁 1于卉影1

作者信息

  • 1. 中国人民解放军北部战区总医院基础医学实验室,沈阳 110003
  • 折叠

摘要

Abstract

Objective To investigate the role of Polo-like kinase 1(PLK1)in cervical cancer cells with different TP53 genotypes.Methods C33a cells(TP53 mutant type)and SiHa cells(TP53 wild type)were treated with the PLK1 inhibitor GSK461364 at 0 nmol/L(control group),2.5 nmol/L(low-concentration group),or 5 nmol/L(high-concentration group)for 24 h.Cell proliferation,cell cycle distri-bution,stemness,and the expression of cell cycle-related proteins were assessed.GEPIA and TCGA databases were used to analyze PLK1 expression and its clinical significance.Results GSK461364 inhibited C33a cell proliferation,induced G2-phase arrest in both cell lines,and attenuated spheroid formation capacity.In C33a cells,both the low-and high-concentration groups showed significantly decreased expression of P-cdc25c,cdc25c,and E2F-1(P<0.05),whereas FoxO1 expression was significantly decreased only in the high-concen-tration group(P<0.05).In SiHa cells,the high-concentration group showed significantly downregulated expression of P-cdc25c,E2F-1,and FoxO1(P<0.05).PLK1 was highly expressed in cervical cancer.Patients with low PLK1 or FoxO1 expression exhibited significantly longer progression-free survival than those with high expression(P<0.05).Conclusion PLK1 inhibition suppressed cell proliferation,induced cell cycle arrest,and impaired spheroid formation in cervical cancer cells,with differential effects according to TP53 genotype.

关键词

Polo样激酶1/宫颈癌/细胞增殖/细胞周期

Key words

Polo-like kinase 1/cervical cancer/cell proliferation/cell cycle

分类

医药卫生

引用本文复制引用

孟繁杰,周丽,邢思宁,于卉影..PLK1在不同TP53基因型宫颈癌细胞中的作用[J].中国医科大学学报,2026,55(8):687-692,6.

基金项目

辽宁省科学技术计划(2023-MS-037) (2023-MS-037)

沈阳市科技计划(24-214-3-173) (24-214-3-173)

中国医科大学学报

0258-4646

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