دورية أكاديمية

RNF8 depletion attenuates hepatocellular carcinoma progression by inhibiting epithelial-mesenchymal transition and enhancing drug sensitivity

التفاصيل البيبلوغرافية
العنوان: RNF8 depletion attenuates hepatocellular carcinoma progression by inhibiting epithelial-mesenchymal transition and enhancing drug sensitivity
المؤلفون: Kuang Jingyu, Duan Ting, Gao Changsong, Liu Chuanyang, Chen Si, Zhu Lv-yun, Min Lu, Lu Chenyu, Wang Wenlun, Zhu Lingyun
المصدر: Acta Biochimica et Biophysica Sinica, Vol 55, Pp 661-671 (2023)
بيانات النشر: China Science Publishing & Media Ltd., 2023.
سنة النشر: 2023
المجموعة: LCC:Biochemistry
LCC:Genetics
مصطلحات موضوعية: hepatocellular carcinoma, epithelial-mesenchymal transition, RNF8, drug resistance, Biochemistry, QD415-436, Genetics, QH426-470
الوصف: Despite substantial advances that have been made in understanding the etiology of hepatocellular carcinoma (HCC), the early-stage diagnosis and treatment of advanced-stage HCC remain a major challenge. RNF8, an E3 ligase important for the DNA damage response, has been proven to facilitate the progression of breast and lung cancer, but its role in HCC remains unclear. In this study, we find that the expression of RNF8 is up-regulated in HCC tissues and positively correlated with poor prognosis of HCC. Furthermore, silencing RNF8 by siRNAs attenuates the migration of HCC cells and inhibits epithelial-mesenchymal transition (EMT) by regulating the expressions of proteins including N-cadherin, β-catenin, snail, and ZO-1. Moreover, Kaplan‒Meier survival analysis shows that high RNF8 expression predicts poor survival benefits from sorafenib. Finally, cell viability assay demonstrates that RNF8 depletion enhances the sensitivity of HCC cells to sorafenib and lenvatinib treatment. We hypothesize that the inhibitory role of RNF8 in EMT and its enhancing effects on anti-cancer drugs orchestrate the protective effects of RNF8 deficiency in HCC, which indicates its potential in clinical application.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1672-9145
Relation: https://doaj.org/toc/1672-9145
DOI: 10.3724/abbs.2023076
URL الوصول: https://doaj.org/article/068e7186c0b2457ebc6b75640d26b484
رقم الأكسشن: edsdoj.068e7186c0b2457ebc6b75640d26b484
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16729145
DOI:10.3724/abbs.2023076