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作 者:Niangmei Cheng Xiaoyuan Zheng Jingyun Huang FeiWang Yang Wang Yue Zhong Yingchao Wang Gaoxiong Wang Bixing Zhao
机构地区:[1]The United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province,Mengchao Hepatobiliary Hospital of Fujian Medical University,Fuzhou 350025,P.R.China [2]Mengchao Med-X Center,Fuzhou University,Fuzhou 350116,P.R.China [3]Department of Surgery,Quanzhou Maternity and Children's Hospital,700 Fengze Street,Quanzhou,Fujian,China [4]Department of General Surgery,the Second AffiliatedHospital,Fujian Medical University,Quanzhou,Fujian,China
出 处:《Oncology and Translational Medicine》2024年第2期66-72,共7页肿瘤学与转化医学(英文版)
基 金:the Natural Science Foundation of Fujian Province(2021 J01539,2023 J011467);Scientific Foundation of the Fuzhou Health Commission(2021-S-wq21,2021-S-wp1).
摘 要:Background:The role of TROVE domain family member 2(TROVE2)has been well-demonstrated in autoimmune diseases;however,its involvement in liver cancer remains unclear.Therefore,this study aimed to explore the biological function and clinical significance of TROVE2 in hepatocellular carcinoma(HCC).Methods:The expression level of TROVE2 was analyzed in HCC and paired adjacent tissue samples using real-time reverse transcription-quantitative polymerase chain reaction.The impact of TROVE2 on migration and invasion in HCC cells was analyzed through Transwell assays and Western blotting.High-throughput transcriptome sequencing and bioinformatics analyses were performed to identify downstream target genes.Back-complementation experiments were employed to verify the influence of downstream proteins on TROVE2-induced invasion and migration of HCC cells.Results:TROVE2 exhibited significant overexpression in liver cancer tissue,correlating with shorter overall survival.Overexpression of TROVE2 facilitated the invasion,metastasis,and epithelial-mesenchymal transition(EMT)process of HCC cells,whereas TROVE2 knockdown restrained migration,invasion,and EMT in these cells.Transcriptome sequencing and bioinformatics analysis identified heparanase(HPSE)as a downstreamtarget protein of TROVE2.Subsequent back-complementation experiments provided evidence that HPSE overexpression promoted TROVE2-mediated prometastasis effects.Moreover,the study revealed that TROVE2 was capable of regulating the EMT pathway through GSK-3βphosphorylation.Conclusions:TROVE2 facilitated the invasion,migration,and EMT process ofHCC cells through phosphorylation of the HPSE/GSK-3βaxis,indicating its significance as an important protein in tumor progression.
关 键 词:Epithelial-mesenchymal transition(EMT) Heparanase(HPSE) Hepatocellular carcinoma(HCC) TROVE2
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