Evidence map›Paper›PMID 18945670›Full record

ArticleThe Journal of biological chemistry2008

Loss of androgen receptor in aging and oxidative stress through Myb protooncoprotein-regulated reciprocal chromatin dynamics of p53 and poly(ADP-ribose) polymerase PARP-1.

Liheng Shi, Soyoung Ko, Soyoung Kim, Ibtissam Echchgadda, Tae-Sung Oh, Chung S Song, Bandana Chatterjee

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  7. An update on PARP inhibitors--moving to the adjuvant setting.Nature reviews. Clinical oncology · 2015
    Review
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  19. T2DM: Why Epigenetics?Journal of nutrition and metabolism · 2011
    Article
  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

7 authors at 1 institution in 1 country.

Liheng ShiDepartment of Molecular Medicine/Institute of Biotechnology, The University of Texas Health Science Center, San Antonio, Texas 78245, USA.
Soyoung Ko
Soyoung Kim
Ibtissam Echchgadda
Tae-Sung Oh
Chung S Song
Bandana Chatterjee
The University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
AGING AND ANDROGEN RECEPTOR GENE REGULATIONR01AG010486 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHATTERJEE, BANDANA · 1993 to 2007
$1.1M
AGING AND ANDROGEN RECEPTOR GENE REGULATIONR37AG010486 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROY, ARUN K. · 1998 to 2003
$1.1M
Aging and Prostatic Hyperplasia in Transgenic MiceR01AG019660 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI CHATTERJEE, BANDANA · 2002 to 2005
$1.0M
NCI NIH HHS 7P30CA54174-14NCI NIH HHS P30 CA054174NIA NIH HHS AG-10486NIA NIH HHS AG-19660NIA NIH HHS R01 AG010486NIA NIH HHS R01 AG019660
6 · The paper itself

Abstract

Poly(ADP-ribosyl)ation of transcription factors and coregulators, mediated by the poly(ADP-ribose) polymerase PARP-1, has been emerging as an important epigenetic mechanism that controls transcriptional dynamics in response to diverse intra- and extracellular signals. PARP-1 activity is also implicated in the regulation of mammalian lifespan. Herein we show that transcriptional down-regulation of androgen receptor (AR) in the aging rat liver and in oxidatively stressed hepatoma cells involves exchange of a PARP-1-associated, p/CAF-containing coactivator assembly for a p53-interacting, Groucho/TLE1-, and mSin3A-included corepressor complex at an age- and oxidant-responsive DNA element (age-dependent factor (ADF) element) in the AR promoter. The coregulator switch is mediated by B-Myb and c-Myb, which bind to the ADF element and physically associate with PARP-1 and the tumor suppressor p53. Heterogeneous nuclear ribonucleoprotein K, residing at the ADF element in association with PARP-1, may serve a platform role in stabilizing the activating complex. PARP-1 coactivated B-Myb- and c-Myb-mediated transactivation of the AR promoter, and p53 antagonized the B-Myb/c-Myb-induced AR promoter activation. PARP-1, heterogeneous nuclear ribonucleoprotein K, B-Myb, and c-Myb each serves as a positive regulator of cellular AR content, whereas p53 negatively regulates AR expression. Our results identify a shared, PARP-1-regulated sensing mechanism that coordinates transcriptional repression of AR during aging and in response to oxidative stress. This study may provide insights as to how advancing age and intracellular redox balance might influence androgen-regulated physiology.

Indexed as

Oxidative StressAgingAnimalsCell NucleusGlutathione TransferaseHeLa CellsHeterogeneous-Nuclear Ribonucleoprotein KHumansModels, BiologicalPoly(ADP-ribose) PolymerasesProto-Oncogene Proteins c-mybRatsRats, Inbred F344Receptors, AndrogenTumor Suppressor Protein p53Glutathione TransferaseHeterogeneous-Nuclear Ribonucleoprotein KPoly(ADP-ribose) PolymerasesProto-Oncogene Proteins c-mybReceptors, AndrogenTumor Suppressor Protein p53

Identifiers

PMID18945670
PMCPMC2606006
OpenAlexW2036422824

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.