Evidence map›Paper›PMID 19383894›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2009

Genetic polymorphisms in the catechol estrogen metabolism pathway and breast cancer risk.

Kerryn W Reding, Noel S Weiss, Chu Chen, Christopher I Li, Christopher S Carlson, Hui-Wen Wilkerson, Federico M Farin, Kenneth E Thummel, Janet R Daling, Kathleen E Malone

Open access · bronzeAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 6 pooled it
3.0field-weighted citation impact, top 8% 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, 6 syntheses or guidelines pooled it, 49 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Kerryn W RedingUniversity of Washington, Seattle, WA 98109, USA. kreding@u.washington.edu
Noel S Weiss
Chu Chen
Christopher I Li
Christopher S Carlson
Hui-Wen Wilkerson
Federico M Farin
Kenneth E Thummel
Janet R Daling
Kathleen E Malone
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
Developing Data-Driven Cancer ResearchersT32CA009168 · NCI · UNIVERSITY OF WASHINGTON · PI STEPHEN M SCHWARTZ, MICHAEL Chiao-An WU · 1985 to 2026
$10.1M
CALCIUM CHANNEL BLOCKERS IN BREAST CANCER ETIOLOGYR01CA072787 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DALING, JANET R · 1997 to 2001
$704k
NCI NIH HHS 2 T32 CA 09168NCI NIH HHS R01 CA072787NCI NIH HHS R01 CA72787NCI NIH HHS T32 CA009168NIEHS NIH HHS P30 ES007033NIEHS NIH HHS P30ES07033
6 · The paper itself

Abstract

backgroundThis study investigated whether single nucleotide polymorphisms (SNP) in genes within the catechol estrogen metabolism pathway altered the risk of breast cancer alone or in combination, as well as whether menopausal hormone therapy modified the effect of these SNPs on breast cancer risk.

methodsIn a population-based case-control study of breast cancer, 891 cases and 878 controls were genotyped for six functional SNPs in the COMT, CYP1B1, GSTM1, GSTP1, and GSTT1 genes.

resultsWomen homozygous with the T allele in CYP1B1*2 (Ser(119); rs1056827) were at 1.69 (95% confidence interval, 1.17-2.46) times the risk of women homozygous with the G allele; women homozygous with the G allele in GSTP1 (Val(105); rs1695) were at 0.73 (95% confidence interval, 0.54-0.99) times the risk of breast cancer compared with women homozygous with the A allele. No other SNPs tested were associated with breast cancer to any appreciable degree. Potential gene-gene and gene-hormone therapy interactions were investigated.

conclusionWith the exception of GSTP1 and possibly CYP1B1*2, our findings do not provide support for the role of genetic variation in the catechol estrogen metabolism pathway and breast cancer risk in postmenopausal women.

Indexed as

Polymorphism, Single NucleotideAgedAllelesAryl Hydrocarbon HydroxylasesBreast NeoplasmsCase-Control StudiesCatechol O-MethyltransferaseCytochrome P-450 CYP1B1Estrogens, CatecholFemaleGenetic Predisposition to DiseaseGlutathione S-Transferase piGlutathione TransferaseHaplotypesHumansPostmenopauseAryl Hydrocarbon HydroxylasesCatechol O-MethyltransferaseCYP1B1 protein, humanCytochrome P-450 CYP1B1Estrogens, CatecholGlutathione S-Transferase piglutathione S-transferase T1Glutathione TransferaseGSTP1 protein, human

Identifiers

PMID19383894
PMCPMC2764317
OpenAlexW2145400787

What OpenQuestion holds

Textmetadata
LicenceTDM
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.