Evidence map›Paper›PMID 24067374›Full record

ArticleCell cycle (Georgetown, Tex.)2013

Tumor protein translationally controlled 1 is a p53 target gene that promotes cell survival.

Weimin Chen, Huihui Wang, Shasha Tao, Yi Zheng, Wei Wu, Fangru Lian, Melba Jaramillo, Deyu Fang, Donna D Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Weimin ChenDepartment of Pharmacology & Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ, USA.
Huihui Wang
Shasha Tao
Yi Zheng
Wei Wu
Fangru Lian
Melba Jaramillo
Deyu Fang
Donna D Zhang
University of Arizona · USChina Academy of Chinese Medical Sciences · CN

Funding

SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI DEAN BILLHEIMER · 1994 to 2026
$36.7M
Training in Environmental Toxicology of Human DiseaseT32ES007091 · NIEHS · UNIVERSITY OF ARIZONA · PI Nathan J Cherrington · 1985 to 2026
$10.7M
The protective role of Nrf2 in arsenic-induced toxicity and carcinogenicityR01ES015010 · NIEHS · UNIVERSITY OF ARIZONA · PI ZHANG, DONNA D · 2006 to 2015
$3.4M
The roles of Sirt1, a deacetylase, in immune tolerance and autoimmunityR01AI079056 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI FANG, DEYU · 2008 to 2017
$3.3M
Investigation of an anti-cancer phytochemical targeting Nrf2R01CA154377 · NCI · UNIVERSITY OF ARIZONA · PI ZHANG, DONNA D · 2011 to 2015
$1.5M
NCI NIH HHS R01 CA154377NCI NIH HHS R01CA154377NIAID NIH HHS R01 AI079056NIAID NIH HHS R01AI079056NIEHS NIH HHS 2R01ES015010NIEHS NIH HHS P30 ES006694NIEHS NIH HHS R01 ES015010NIEHS NIH HHS T32 ES007091
6 · The paper itself

Abstract

Tumor suppressor p53 maintains genome stability by differentially activating target genes that control diverse cellular responses, such as the antioxidant response, cell cycle arrest and apoptosis. Despite the fact that many p53 downstream genes have been well characterized, novel p53 target genes are continuously being identified. Here, we report that Tpt1 is a direct target gene of p53. We found that p53 upregulates the transcription of Tpt1 and identified a p53-responsive element in the promoter of the mouse Tpt1 gene. Furthermore, p53-dependent induction of Tpt1 was able to reduce oxidative stress, minimize apoptosis, and promote cell survival in response to H 2O2 challenge. In addition, a positive correlation between the expression of p53 and Tpt1 only existed in normal lung tissues, not in lung tumors. Such positive correlation was also found in lung cell lines that contain wild-type p53, but not mutated p53. Based on the important role of Tpt1 in cancer development, chemoresistance, and cancer reversion, identification of Tpt1 as a direct target gene of p53 not only adds to the complexity of the p53 network, but may also open up a new avenue for cancer prevention and intervention.

Indexed as

Gene Expression Regulation, NeoplasticResponse ElementsAnimalsApoptosisBase SequenceBiomarkers, TumorCell Line, TumorCell SurvivalGene Expression ProfilingGenes, ReporterHumansHydrogen PeroxideLuciferasesLungLung NeoplasmsMiceBiomarkers, TumorHydrogen PeroxideLuciferasesTPT1 protein, humanTpt1 protein, mouseTumor Protein, Translationally-Controlled 1Tumor Suppressor Protein p53cancerp53TCTPTpt1

Identifiers

PMID24067374
PMCPMC3755082
OpenAlexW2040401741

What OpenQuestion holds

Textmetadata
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.