Evidence map›Paper›PMID 23824676›Full record

ArticleInternational journal of cancer2014

CYP2B6*6 is associated with increased breast cancer risk.

Christina Justenhoven, Daniela Pentimalli, Sylvia Rabstein, Volker Harth, Anne Lotz, Beate Pesch, Thomas Brüning, Thilo Dörk, Peter Schürmann, Natalia Bogdanova and 15 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in International journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

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  16. Discriminatory power of common genetic variants in personalized breast cancer diagnosis.Proceedings of SPIE--the International Society for Optical Engineering · 2016
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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

25 authors at 13 institutions in 4 countries.

Christina JustenhovenDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, University of Tübingen, Stuttgart, Germany.
Daniela Pentimalli
Sylvia Rabstein
Volker Harth
Anne Lotz
Beate Pesch
Thomas Brüning
Thilo Dörk
Peter Schürmann
Natalia Bogdanova
Tjoung-Won Park-Simon
Fergus J Couch
Janet E Olson
Peter A Fasching
Matthias W Beckmann
Lothar Häberle
Arif Ekici
Per Hall
Kamilla Czene
Janjun Liu
Jingmei Li
Christian Baisch
Ute Hamann
Yon-Dschun Ko
Hiltrud Brauch
Medizinische Hochschule Hannover · DERuhr University Bochum · DEUniversitätsklinikum Erlangen · DEGenome Institute of Singapore · SGJohanniter-Krankenhaus Bonn · DEKarolinska Institutet · SEMayo Clinic in Florida · USUniversity of Tübingen · DEDKFZ-ZMBH Alliance · DEDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DEInstitute for Prevention and Occupational Medicine · DEUniversity Medical Center Hamburg-Eppendorf · DEUniversity of California, Los Angeles · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
A genome-wide association study for breast cancer in BRCA1 mutation carriersR01CA128978 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2008 to 2012
$4.8M
HORMONE REPLACEMENT THERAPY AND BREAST CANCERR01CA058427 · NCI · UPPSALA UNIVERSITY · PI ADAMI, HANS-OLOV · 1993 to 1995
–
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA128978NCI NIH HHS R01 CA58427
6 · The paper itself

Abstract

The cytochrome P450 2B6 (CYP2B6) is involved in the metabolism of testosterone. Functional changes in this enzyme may influence endogenous hormone exposure, which has been associated with risk of breast cancer. To assess potential associations between two functional polymorphisms CYP2B6_516_G>T (rs3745274) and CYP2B6_785_A>G (rs2279343) and breast cancer risk, we established a specific matrix-assisted laser desorption/ionization time-of-flight mass spectrometry assay. The GENICA breast cancer case-control study showed associations between the variant genotypes CYP2B6_516_TT and CYP2B6_785_GG and breast cancer risk with odds ratios (ORs) of 1.34 (p = 0.001) and 1.31 (p = 0.002), respectively. A similar effect was observed for carriers of the CYP2B6_516_T allele in a validation study including four independent studies from Germany, Sweden and USA. In a pooled analysis of all five studies involving 4,638 breast cancer cases and 3,594 controls of European ancestry, carriers of the CYP2B6_516_G and the CYP2B6_785_G variant had an increased breast cancer risk with ORs of 1.10 (p = 0.027) and 1.10 (p = 0.031), respectively. We conclude that the genetic variants CYP2B6_516_G and CYP2B6_785_G (designated CYP2B6*6), which are known to decrease activity of the CYP2B6 enzyme, contribute to an increased breast cancer risk.

Indexed as

Genetic Predisposition to DiseaseAdultAgedAged, 80 and overAryl Hydrocarbon HydroxylasesBiomarkers, TumorBreast NeoplasmsCase-Control StudiesCytochrome P-450 CYP2B6FemaleFollow-Up StudiesGenotypeHumansMeta-Analysis as TopicMiddle AgedPolymorphism, GeneticAryl Hydrocarbon HydroxylasesBiomarkers, TumorCYP2B6 protein, humanCytochrome P-450 CYP2B6breast cancer riskCYP2B6polymorphismtestosterone

Identifiers

PMID23824676
PMCPMC3883876
OpenAlexW1507747075

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.