Evidence map›Paper›PMID 17160017›Full record

ArticleOncogene2007

Protective roles of quinone reductase and tamoxifen against estrogen-induced mammary tumorigenesis.

M M Montano, L J Chaplin, H Deng, S Mesia-Vela, N Gaikwad, M Zahid, E Rogan

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 23% 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

26 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Inhibitory Effects of γ- and δ-Tocopherols on Estrogen-Stimulated Breast CancerCancer prevention research (Philadelphia, Pa.) · 2017
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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
  12. Article
  13. TARGETING THE GENOTOXIC EFFECTS OF ESTROGENS.Drug discovery today. Disease mechanisms · 2012
    Article
  14. The etiology and prevention of breast cancer.Drug discovery today. Disease mechanisms · 2012
    Article
  15. Article
  16. Unbalanced metabolism of endogenous estrogens in the etiology and prevention of human cancer.The Journal of steroid biochemistry and molecular biology · 2011
    Review
  17. Article
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 1 country.

M M MontanoDepartment of Pharmacology, Case Western Reserve University, Cleveland, OH 44106, USA. mxm126@po.cwru.edu
L J Chaplin
H Deng
S Mesia-Vela
N Gaikwad
M Zahid
E Rogan
Case Western Reserve University · USUniversity of Nebraska Medical Center · USColumbia University · US

Funding

UNIFYING INITIATION MECHANISM OF BREAST/PROSTATE CANCERP01CA049210 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CAVALIERI, ERCOLE L · 1989 to 2004
$3.3M
A Novel Growth Regulatory Factor in Breast CellsR01CA092440 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MONTANO, MONICA · 2002 to 2012
$3.0M
NCI NIH HHS CA80959NCI NIH HHS CA92440NCI NIH HHS P01 CA49210NIEHS NIH HHS ES05022
6 · The paper itself

Abstract

We previously reported that antiestrogen-liganded estrogen receptor beta (ERbeta) transcriptionally activates the major detoxifying enzyme quinone reductase (QR) (NAD(P)H:quinone oxidoreductase). Further studies on the functional role of ERbeta-mediated upregulation of antioxidative enzymes indicated protective effects against estrogen-induced oxidative DNA damage (ODD). We now report on in vivo and in vitro studies that show that ERbeta-mediated upregulation of QR are involved in the protection against estrogen-induced mammary tumorigenesis. Using the August Copenhagen Irish (ACI) model of estrogen-induced carcinogenesis, we observed that increased ODD and decreased QR expression occur early in the process of estrogen-induced mammary tumorigenesis. Prevention of ACI mammary gland tumorigenesis by tamoxifen was accompanied by decreased ODD and increased QR levels. These correlative findings were supported by our findings that downregulation of QR levels led to increased levels of estrogen quinone metabolites and enhanced transformation potential of 17beta-estradiol treated MCF10A non-tumorigenic breast epithelial cells. Concurrent expression of ERbeta and treatment with 4-hydroxytamoxifen decreased tumorigenic potential of these MCF10A cells. We conclude that upregulation of QR, through induction by tamoxifen, can inhibit estrogen-induced ODD and mammary cell tumorigenesis, representing a possible novel mechanism of tamoxifen prevention against breast cancer.

Indexed as

8-Hydroxy-2'-DeoxyguanosineAnimalsBreast NeoplasmsCell Transformation, NeoplasticDeoxyguanosineDNA DamageEstrogen AntagonistsEstrogen Receptor betaEstrogensHumansMammary Glands, AnimalNAD(P)H Dehydrogenase (Quinone)Oxidative StressRatsTamoxifenTumor Cells, Cultured8-Hydroxy-2'-DeoxyguanosineafimoxifeneDeoxyguanosineEstrogen AntagonistsEstrogen Receptor betaEstrogensNAD(P)H Dehydrogenase (Quinone)Tamoxifen

Identifiers

PMID17160017
OpenAlexW2013370943

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.