Evidence map›Paper›PMID 19723627›Full record

ArticleThe Journal of biological chemistry2009

Androgen via p21 inhibits tumor necrosis factor alpha-induced JNK activation and apoptosis.

Fangming Tang, John Kokontis, Yuting Lin, Shutsung Liao, Anning Lin, Jialing Xiang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Androgen receptor as a targeted therapy for breast cancer.American journal of cancer research · 2012
    Article
  10. 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

6 authors at 2 institutions in 1 country.

Fangming TangBen May Department for Cancer Research, University of Chicago, Chicago, Illinois 60637, USA.
John Kokontis
Yuting Lin
Shutsung Liao
Anning Lin
Jialing Xiang
University of Chicago · USIllinois Institute of Technology · US

Funding

MOLECULAR MECHANISMS OF GROWTH CONTROL--PROSTATE CANCERR01CA058073 · NCI · UNIVERSITY OF CHICAGO · PI LIAO, SHUTSUNG · 1992 to 2012
$3.4M
Wiring the UV Signaling CircuitryR01ES015868 · NIEHS · UNIVERSITY OF CHICAGO · PI LIN, ANNING · 2008 to 2012
$1.7M
Differentially Regulating Apoptosis by AR: Activating Bax or Inhibiting JNK MAPKR01CA128114 · NCI · ILLINOIS INSTITUTE OF TECHNOLOGY · PI XIANG, JIALING · 2008 to 2012
$1.5M
Targeting BAD by JNK for Cell SurvivalR01GM071409 · NIGMS · UNIVERSITY OF CHICAGO · PI LIN, ANNING · 2006 to 2009
$1.1M
Prostate Cancer--Mechanisms of Bax induced Cell DeathK01CA090516 · NCI · UNIVERSITY OF CHICAGO · PI XIANG, JIALING · 2001 to 2005
$506k
NCI NIH HHS CA090516NCI NIH HHS CA128114NCI NIH HHS K01 CA090516NCI NIH HHS R01 CA058073NCI NIH HHS R01 CA128114NIEHS NIH HHS ES015868NIEHS NIH HHS R01 ES015868NIGMS NIH HHS GM71409NIGMS NIH HHS R01 GM071409
6 · The paper itself

Abstract

The male hormone androgen is a growth/survival factor for its target tissues or organs. Yet, the underlying mechanism is incompletely understood. Here, we report that androgen via p21 inhibits tumor necrosis factor alpha-induced JNK activation and apoptosis. Inhibition by androgen requires the transcription activity of androgen receptor (AR) and de novo protein synthesis. Androgen.AR induces expression of p21 that in turn inhibits tumor necrosis factor alpha-induced JNK and apoptosis. Furthermore, genetic interruption of p21 alleles abolishes the inhibition by androgen. Our results reveal a novel cross-talk between androgen x AR and JNK, thereby providing a molecular mechanism underlying the survival function of androgen.

Indexed as

Gene Expression Regulation, NeoplasticAllelesAndrogensApoptosisCell Line, TumorCyclin-Dependent Kinase Inhibitor p21Enzyme ActivationHumansMaleMAP Kinase Kinase 4Models, BiologicalProstatic NeoplasmsReceptors, AndrogenTranscription, GeneticTumor Necrosis Factor-alphaAndrogensAR protein, humanCyclin-Dependent Kinase Inhibitor p21MAP Kinase Kinase 4Receptors, AndrogenTumor Necrosis Factor-alpha

Identifiers

PMID19723627
PMCPMC2781650
OpenAlexW2051020921

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.