Evidence map›Paper›PMID 15731171›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2005

The androgen receptor directly targets the cellular Fas/FasL-associated death domain protein-like inhibitory protein gene to promote the androgen-independent growth of prostate cancer cells.

Shen Gao, Peng Lee, Hua Wang, William Gerald, Michael Adler, Liying Zhang, Yun-Fang Wang, Zhengxin Wang

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 75 citations in OpenAlex.

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  16. Elevation of c-FLIP in castrate-resistant prostate cancer antagonizes therapeutic response to androgen receptor-targeted therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2012
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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

8 authors at 4 institutions in 1 country.

Shen GaoDepartment of Cancer Biology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 173, Houston, TX 77030-4009, USA.
Peng Lee
Hua Wang
William Gerald
Michael Adler
Liying Zhang
Yun-Fang Wang
Zhengxin Wang
The University of Texas MD Anderson Cancer Center · USMemorial Sloan Kettering Cancer Center · USNew York University · USVA NY Harbor Healthcare System · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
SPORE In Prostate CancerP50CA092629 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Yu Chen, MICHAEL J MORRIS · 2001 to 2026
$63.0M
Mechanisms of action of androgen receptor and cofactorsR01DK065156 · NIDDK · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WANG, ZHENGXIN · 2003 to 2007
$1.4M
NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA092629NIDDK NIH HHS 1R01 DK065156 01NIDDK NIH HHS R01 DK065156
6 · The paper itself

Abstract

Androgens provide survival signals to prostate epithelial cells, and androgen ablation induces apoptosis in the prostate gland. However, the molecular mechanisms of actions of the androgen-signaling pathway in these processes are not fully understood. Here, we report that androgens induced expression of the cellular Fas/FasL-associated death domain protein-like inhibitory protein (c-FLIP) gene, which is a potent inhibitor of Fas/FasL-mediated apoptosis. The androgen receptor was recruited to the promoter of the c-FLIP gene in the presence of androgens. We found that c-FLIP promoter contained multiple functional androgen response elements. In addition, we show that c-FLIP overexpression accelerated progression to androgen independence by inhibiting apoptosis in LNCaP prostate tumors implanted in nude mice. Our results suggest that the androgen receptor affects survival and apoptosis of prostate cells through regulation of the c-FLIP gene in response to androgens.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptional ActivationAndrogensAnimalsApoptosisBase SequenceCASP8 and FADD-Like Apoptosis Regulating ProteinFas Ligand ProteinHumansIntracellular Signaling Peptides and ProteinsMaleMembrane GlycoproteinsMiceMolecular Sequence DataOligonucleotide Array Sequence AnalysisPromoter Regions, GeneticAndrogensCASP8 and FADD-Like Apoptosis Regulating ProteinCFLAR protein, humanCflar protein, mouseFASLG protein, humanFas Ligand ProteinFasl protein, mouseIntracellular Signaling Peptides and ProteinsMembrane GlycoproteinsReceptors, Androgen

Identifiers

PMID15731171
PMCPMC1855294
OpenAlexW2063298842

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.