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  4. Metastatic tumor antigen 1 contributes to hepatocarcinogenesis posttranscriptionally through RNA-binding function
 
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Metastatic tumor antigen 1 contributes to hepatocarcinogenesis posttranscriptionally through RNA-binding function

Journal
Hepatology
Journal Volume
77
Journal Issue
2
Pages
379
Date Issued
2023
Author(s)
Li Y.-T.
CHUN-JEN LIU  
JIA-HORNG KAO  
Lin L.-F.
Tu H.-C.
Wang C.-C.
Huang P.-H.
Cheng H.-R.
PEI-JER CHEN  
DING-SHINN CHEN  
Wu H.-L.
DOI
10.1002/hep.32356
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124620273&doi=10.1002%2fhep.32356&partnerID=40&md5=9e064dc7378067515ed52602aef3726a
https://scholars.lib.ntu.edu.tw/handle/123456789/619210
Abstract
BACKGROUND AND AIMS: Both nuclear and cytoplasmic overexpression of metastatic tumor antigen 1 (MTA1) contributes to tumorigenesis of HCC. Most studies have focused on nuclear MTA1 whose function is mainly a chromatin modifier regulating the expression of various cancer-promoting genes. By contrast, the molecular mechanisms of cytoplasmic MTA1 in carcinogenesis remain elusive. Here, we reveal a role of MTA1 in posttranscriptional gene regulation. APPROACH AND RESULTS: We conducted the in vitro and in vivo RNA-protein interaction assays indicating that MTA1 could bind directly to the 3'-untranslated region of MYC RNA. Mutation at the first glycine of the conserved GXXG loop within a K-homology II domain-like structure in MTA1 (G78D) resulted in the loss of RNA-binding activity. We used gain- and loss-of-function strategy showing that MTA1, but not the G78D mutant, extended the half-life of MYC and protected it from the lethal -7-mediated degradation. The G78D mutant exhibited lower activity in promoting tumorigenesis than wild-type in vitro and in vivo. Furthermore, RNA-immunoprecipitation sequencing analysis demonstrated that MTA1 binds various oncogenesis-related mRNAs besides MYC . The clinical relevance of cytoplasmic MTA1 and its interaction with MYC were investigated using HBV-HCC cohorts with or without early recurrence. The results showed that higher cytoplasmic MTA1 level and MTA1- MYC interaction were associated with early recurrence. CONCLUSIONS: MTA1 is a generic RNA-binding protein. Cytoplasmic MTA1 and its binding to MYC is associated with early recurrence in patients with HBV-HCC. This function enables it to regulate gene expression posttranscriptionally and contributes to hepatocarcinogenesis.
SDGs

[SDGs]SDG3

Publisher
John Wiley and Sons Inc
Type
journal article

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