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hMSH2 coordinated with the expression of E2F1 promotes platinum response in epithelial ovarian cancer
被引:0
作者:
Hu, Xiao-qian
[1
]
Zhang, Bao-ying
[2
]
Hua, Tian
[2
,3
]
机构:
[1] Hebei Med Univ, Dept Oncol, Affiliated Xingtai People Hosp, Xingtai, Peoples R China
[2] Hebei Med Univ, Affiliated Xingtai People Hosp, Dept Gynaecol, Xingtai, Peoples R China
[3] Hebei Med Univ, Dept Gynaecol, Affiliated Xingtai People Hosp, Hongxing Rd 16, Xingtai 054001, Peoples R China
关键词:
hMSH2;
Mismatch repair;
Transcription factors;
Platinum resistance;
TRANSCRIPTION FACTORS;
CLINICAL-RELEVANCE;
DNA-REPAIR;
REPLICATION;
APOPTOSIS;
FAMILY;
CELLS;
D O I:
10.1177/03000605231163780
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
ObjectiveTo explore underlying mechanisms that regulate hMSH2 expression and drug susceptibility in epithelial ovarian cancer (EOC). MethodsUsing data from the Cancer Genome Atlas (TCGA) we used bioinformatical analysis to predict transcription factors (TFs) that potentially regulate hMSH2. RT-qPCR, Western blot, and luciferase assays were undertaken using ovarian cancer cell lines to verify the identified TF. Expressions of the TF were modulated using overexpression or knockdown, and the corresponding cellular responses to cisplatin were examined. ResultsThe TF, E2F1, was found to regulate the hMSH2 gene. The expression level of E2F1 correlated with cisplatin susceptibility in vitro. Kaplan-Meier analysis of 77 patients with EOC showed that low E2F1 expression was associated with worse survival. ConclusionsTo our knowledge, this is the first report of E2F1 regulated MSH2 expression playing a role in drug resistance of platinum-based treatments for patients with EOC. Further work is need to confirm our results.
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页数:14
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