Evidence map›Paper›PMID 18663360›Full record

ArticleOncogene2008

hPMC2 is required for recruiting an ERbeta coactivator complex to mediate transcriptional upregulation of NQO1 and protection against oxidative DNA damage by tamoxifen.

S P Sripathy, L J Chaplin, N W Gaikwad, E G Rogan, M M Montano

Abstract read
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Transcriptional roles of PARP1 in cancer.Molecular cancer research : MCR · 2014
    Review
  6. Article
  7. Article
  8. Induction of quinone reductase by tamoxifen or DPN protects against mammary tumorigenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  9. Article
  10. The effect of tamoxifen and raloxifene on estrogen metabolism and endometrial cancer risk.The Journal of steroid biochemistry and molecular biology · 2011
    Article
  11. Tamoxifen increases nuclear respiratory factor 1 transcription by activating estrogen receptor beta and AP-1 recruitment to adjacent promoter binding sites.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
  12. Article
  13. Review
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

5 authors at 2 institutions in 1 country.

S P SripathyDepartment of Pharmacology, Case Western Reserve University, Cleveland, OH 44106, USA.
L J Chaplin
N W Gaikwad
E G Rogan
M M Montano
Case Western Reserve University · USUniversity of Nebraska Medical Center · US

Funding

A Novel Growth Regulatory Factor in Breast CellsR01CA092440 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MONTANO, MONICA · 2002 to 2012
$3.0M
Determinants of Chemoprevention by SERMsR03CA130066 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MONTANO, MONICA · 2007 to 2008
$155k
NCI NIH HHS CA130066NCI NIH HHS CA92440NCI NIH HHS R01 CA092440NCI NIH HHS R03 CA130066
6 · The paper itself

Abstract

In the presence of ERbeta, trans-hydroxytamoxifen (TOT) protects cells against 17beta-estradiol (E(2))-induced oxidative DNA damage (ODD) and this correlates with increased expression of the antioxidative enzyme quinone reductase (QR). Here, we investigate the molecular mechanism responsible for ERbeta-mediated protection against ODD. We observe constitutive interaction between ERbeta and the novel protein hPMC2. Using a combination of breast epithelial cell lines that are either positive or negative for ERalpha, we demonstrate TOT-dependent recruitment of both ERbeta and hPMC2 to the EpRE (electrophile response element)-regulated antioxidative enzyme QR. We further demonstrate TOT-dependent corecruitment of the coactivators Nrf2, PARP-1 (poly (ADP-ribose) polymerase 1) and topoisomerase IIbeta, both in the presence and absence of ERalpha. However, absence of either ERbeta or hPMC2 results in nonrecruitment of PARP-1 and topoisomerase IIbeta, loss of antioxidative enzyme induction and attenuated protection against ODD by TOT even in the presence of Nrf2 and ERalpha. These findings indicate minor role for Nrf2 and ERalpha in TOT-dependent antioxidative gene regulation. However, downregulation of PARP-1 attenuates TOT-dependent antioxidative gene induction. We conclude that ERbeta and hPMC2 are required for TOT-dependent recruitment of coactivators such as PARP-1 to the EpRE resulting in the induction of antioxidative enzymes and subsequent protection against ODD.

Indexed as

DNA DamageBreast NeoplasmsCell Line, TumorDNA-Binding ProteinsDNA Topoisomerases, Type IIEstrogen Receptor betaFemaleGene Expression Regulation, EnzymologicHumansNAD(P)H Dehydrogenase (Quinone)NF-E2-Related Factor 2Oxidative StressPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesResponse ElementsRetroviridaeafimoxifeneDNA-Binding ProteinsDNA Topoisomerases, Type IIEstrogen Receptor betaNAD(P)H Dehydrogenase (Quinone)NFE2L2 protein, humanNF-E2-Related Factor 2NQO1 protein, humanPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesTamoxifenTrans-Activators

Identifiers

PMID18663360
PMCPMC4094353
OpenAlexW2087432120

What OpenQuestion holds

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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.