Evidence map›Paper›PMID 34646425›Full record

ReviewOxidative medicine and cellular longevity2021

ROS Signaling-Mediated Novel Biological Targets: Brf1 and RNA Pol III Genes.

Liling Zheng, Yongluan Lin, Shuping Zhong

RetractedOpen access · hybridAbstract readReviewRetracted Publication
In one paragraph

Review in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Liling ZhengFirst Hospital of Quanzhou Affiliated to Fujian Medical University, China.ORCID https://orcid.org/0000-0002-7746-4722
Yongluan LinKeck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Shuping ZhongKeck School of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID https://orcid.org/0000-0001-6506-7925
University of Southern California · USFujian Medical University · CN

Funding

Molecular mechanism of alcohol-associated liver tumor developmentR01AA024169 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHONG, SHUPING · 2017 to 2021
$1.9M
Mechanism of Alcohol-induced RNA pol III dependent transcriptionR21AA017288 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHONG, SHUPING · 2009 to 2010
$447k
Function of Runx2 in alcohol-associated breast cancerR21AA023247 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHONG, SHUPING · 2014 to 2015
$446k
Role of MSK1, ERa and Brf1 in alcohol-associated breast cancerR21AA021114 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHONG, SHUPING · 2012 to 2013
$434k
NIAAA NIH HHS R01 AA024169NIAAA NIH HHS R21 AA017288NIAAA NIH HHS R21 AA021114NIAAA NIH HHS R21 AA023247
6 · The paper itself

Abstract

Biomolecule metabolism produces ROS (reactive oxygen species) under physiological and pathophysiological conditions. Dietary factors (alcohol) and carcinogens (EGF, DEN, and MNNG) also induce the release of ROS. ROS often causes cell stress and tissue injury, eventually resulting in disorders or diseases of the body through different signaling pathways. Normal metabolism of protein is critically important to maintain cellular function and body health. Brf1 (transcript factor II B-related factor 1) and its target genes, RNA Pol III genes (RNA polymerase III-dependent genes), control the process of protein synthesis. Studies have demonstrated that the deregulation of Brf1 and its target genes is tightly linked to cell proliferation, cell transformation, tumor development, and human cancers, while alcohol, EGF, DEN, and MNNG are able to induce the deregulation of these genes through different signaling pathways. Therefore, it is very important to emphasize the roles of these signaling events mediating the processes of Brf1 and RNA Pol III gene transcription. In the present paper, we mainly summarize our studies on signaling events which mediate the deregulation of these genes in the past dozen years. These studies indicate that Brf1 and RNA Pol III genes are novel biological targets of ROS.

Indexed as

Cell ProliferationCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHumansReactive Oxygen SpeciesRNA Polymerase IIITATA-Binding Protein Associated FactorsBRF1 protein, humanReactive Oxygen SpeciesRNA Polymerase IIITATA-Binding Protein Associated Factors

Identifiers

PMID34646425
PMCPMC8505076
OpenAlexW3201806692

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.