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作 者:Chu-Li Fu Zheng-Wei Zhao Qiang-Nu Zhang
机构地区:[1]Department of Hematology and Oncology,Guangzhou Women and Children’s Medical Center,Guangzhou Medical University,Guangzhou 510623,China [2]Biomedicine Research Center,Guangdong Provincial Key Laboratory of Major Obstetric Disease,Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology,the Third Affiliated Hospital of Guangzhou Medical University,Guangzhou 510150,China
出 处:《Hepatobiliary & Pancreatic Diseases International》2025年第1期67-75,共9页国际肝胆胰疾病杂志(英文版)
基 金:supported by grants from Research Founda-tion of Guangzhou Women and Children’s Medical Center for Clinical Doctor (1600110);Science and Technology Projects in Guangzhou (202201011371);Guangzhou Municipalcience and Tech-nology Bureau Foundation (2023A03J0917);Guangdong Basic and Applied Basic Research Foundation (2023A1515220076 and 2022A1515110283)。
摘 要:Background:Within the tumor microenvironment,survival pressures are prevalent with potent drivers of tumor progression,angiogenesis,and therapeutic resistance.N6-methyladenosine(m6 A)methylation has been recognized as a critical post-transcriptional mechanism regulating various aspects of mRNA metabolism.Understanding the intricate interplay between survival pressures and m6 A modification pro-vides new insights into the molecular mechanisms underlying hepatocellular carcinoma(HCC)progres-sion and highlights the potential for targeting the survival pressures-m6 A axis in HCC diagnosis and treat-ment.Data sources:A literature search was conducted in PubMed,MEDLINE,and Web of Science for relevant articles published up to April 2024.The keywords used for the search included hepatocellular carcinoma,cellular survival,survival pressure,N6-methyladenosine,tumor microenvironment,stress response,and hypoxia.Results:This review delves into the multifaceted roles of survival pressures and m6 A RNA methylation in HCC,highlighting how survival pressures modulate the m6 A landscape,the impact of m6 A modifica-tion on survival pressure-responsive gene expression,and the consequent effects on HCC cell survival,proliferation,metastasis,and resistance to treatment.Furthermore,we explored the therapeutic potential of targeting this crosstalk,proposing strategies that leverage the understanding of survival pressures and m6 A RNA methylation mechanisms to develop novel,and more effective treatments for HCC.Conclusions:The interplay between survival pressures and m6 A RNA methylation emerges as a complex regulatory network that influences HCC pathogenesis and progression.
关 键 词:Hepatocellular carcinoma N6-methyladenosine methylation HYPOXIA Target therapy Survival pressure
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