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Molecular interplay between EIF4 family and circular RNAs in cancer: Mechanisms and therapeutics

The eukaryotic translation initiation factor 4 (EIF4) family is a major contributor to the recruitment of mRNAs to ribosomes during the initial translation stage in eukaryotes, whose dysregulation either allows for cancer transformation or prevents disordered cancerous cell growth. Circular RNAs (ci...

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Bibliographic Details
Published in:European journal of pharmacology 2023-09, Vol.954, p.175867-175867, Article 175867
Main Authors: Song, Jia, Ge, Yuexin, Dong, Mingyan, Guan, Qiutong, Ju, Mingyi, Song, Xueyi, Han, Jiali, Zhao, Lin
Format: Article
Language:English
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Summary:The eukaryotic translation initiation factor 4 (EIF4) family is a major contributor to the recruitment of mRNAs to ribosomes during the initial translation stage in eukaryotes, whose dysregulation either allows for cancer transformation or prevents disordered cancerous cell growth. Circular RNAs (circRNAs), which exhibit distinctive structures and are widely expressed in eukaryotes, are anticipated to be clinical diagnostic biomarkers for cancer therapy. There is considerable evidence that EIF4s can influence the biogenesis, transport, and function of circRNAs and, in turn, circRNAs can control the expressions of EIF4s through certain molecular pathways. Herein, we primarily review the emerging studies of the EIF4 family and pinpoint the roles of dysregulated EIF4s in cancer. We also evaluate the patterns of intricate interactions between circRNAs and EIF4s and discuss the potential utility of circRNA-based therapeutics targeting EIF4s in clinical cancer research. •EIF4 family is responsible for recruiting mRNAs to ribosomes during the eukaryotic translation initiation phase.•EIF4 family can act as either an oncogene or a tumor suppressor in cancer.•EIF4 family participates in cancer development via several regulatory patterns in concert with functional circRNAs.•There are several targeted tumor therapies based on the EIF4-circRNA regulatory network.
ISSN:0014-2999
1879-0712
DOI:10.1016/j.ejphar.2023.175867