Evidence map›Paper›PMID 32932781›Full record

ReviewInternational journal of molecular sciences2020

mRNA Post-Transcriptional Regulation by AU-Rich Element-Binding Proteins in Liver Inflammation and Cancer.

Dobrochna Dolicka, Cyril Sobolewski, Marta Correia de Sousa, Monika Gjorgjieva, Michelangelo Foti

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  14. The Role ofMicroorganisms · 2023
    Review
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  19. The Polyvalent Role of NF90 in RNA Biology.International journal of molecular sciences · 2022
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Dobrochna DolickaDepartment of Cell Physiology and Metabolism and Translational Research Center in Oncohaematology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Cyril SobolewskiDepartment of Cell Physiology and Metabolism and Translational Research Center in Oncohaematology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Marta Correia de SousaDepartment of Cell Physiology and Metabolism and Translational Research Center in Oncohaematology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Monika GjorgjievaDepartment of Cell Physiology and Metabolism and Translational Research Center in Oncohaematology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0001-8553-7525
Michelangelo FotiDepartment of Cell Physiology and Metabolism and Translational Research Center in Oncohaematology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0001-7199-4135
University of Geneva · CH

Funding

Geneva Cancer League 1514 and 1711Swiss Cancer Research foundation KFS-4094-02-2017-RSwiss National Science Foundation 310030-172862
6 · The paper itself

Abstract

AU-rich element-binding proteins (AUBPs) represent important post-transcriptional regulators of gene expression. AUBPs can bind to the AU-rich elements present in the 3'-UTR of more than 8% of all mRNAs and are thereby able to control the stability and/or translation of numerous target mRNAs. The regulation of the stability and the translation of mRNA transcripts by AUBPs are highly complex processes that occur through multiple mechanisms depending on the cell type and the cellular context. While AUBPs have been shown to be involved in inflammatory processes and the development of various cancers, their important role and function in the development of chronic metabolic and inflammatory fatty liver diseases (FLDs), as well as in the progression of these disorders toward cancers such as hepatocellular carcinoma (HCC), has recently started to emerge. Alterations of either the expression or activity of AUBPs are indeed significantly associated with FLDs and HCC, and accumulating evidence indicates that several AUBPs are deeply involved in a significant number of cellular processes governing hepatic metabolic disorders, inflammation, fibrosis, and carcinogenesis. Herein, we discuss our current knowledge of the roles and functions of AUBPs in liver diseases and cancer. The relevance of AUBPs as potential biomarkers for different stages of FLD and HCC, or as therapeutic targets for these diseases, are also highlighted.

Indexed as

3' Untranslated RegionsAnimalsCarcinoma, HepatocellularHumansInflammationLiver NeoplasmsRNA, MessengerRNA Processing, Post-Transcriptional3' Untranslated RegionsRNA, Messengerfibrosishepatocellular carcinomaHuRnonalcoholic steatohepatitisRNA-binding proteinstristetraprolin

Identifiers

PMID32932781
PMCPMC7554771
OpenAlexW3086436083

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.