Evidence map›Paper›PMID 23850146›Full record

ArticleCancer epidemiology2013

No association between genetic variants in angiogenesis and inflammation pathway genes and breast cancer survival among Chinese women.

Tsogzolmaa Dorjgochoo, Ying Zheng, Yu-Tang Gao, Xiangyu Ma, Jirong Long, Pingping Bao, Ben Zhang, Wanqing Wen, Wei Lu, Wei Zheng and 2 more

Abstract read
In one paragraph

Article in Cancer epidemiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

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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

5 citing papers in PubMed.

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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

12 authors.

Tsogzolmaa DorjgochooDivision of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Ying Zheng
Yu-Tang Gao
Xiangyu Ma
Jirong Long
Pingping Bao
Ben Zhang
Wanqing Wen
Wei Lu
Wei Zheng
Xiao Ou Shu
Alicia Beeghly-Fadiel

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
Building Interdisciplinary Research Careers in Women's HealthK12HD043483 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARTMANN, KATHERINE E, MAJOR, AMY S · 2002 to 2023
$10.3M
Shanghai Breast Cancer StudyR01CA064277 · NCI · VANDERBILT UNIVERSITY · PI SHU, XIAO-OU · 1996 to 2012
$4.8M
MOLECULAR EPIDEMIOLOGIC STUDY OF BREAST CANCERR01CA090899 · NCI · VANDERBILT UNIVERSITY · PI ZHENG, WEI · 2000 to 2009
$3.5M
Genetic Factors for Breast Cancer- A genome Wide StudyR01CA124558 · NCI · VANDERBILT UNIVERSITY · PI ZHENG, WEI · 2008 to 2012
$3.1M
Breast Cancer Survival: Lifestyle and Genetic DeterminantsR01CA118229 · NCI · VANDERBILT UNIVERSITY · PI SHU, XIAO-OU · 2007 to 2010
$2.9M
NCI NIH HHS P30 CA068485NCI NIH HHS P30CA68485NCI NIH HHS R01 CA064277NCI NIH HHS R01 CA090899NCI NIH HHS R01 CA118229NCI NIH HHS R01 CA124558NCI NIH HHS R01CA124558NCI NIH HHS R01CA64277NCI NIH HHS R01CA90899NICHD NIH HHS 5K12 HD043483-09NICHD NIH HHS K12 HD043483
6 · The paper itself

Abstract

backgroundAngiogenesis and inflammation are implicated in breast cancer prognosis; however, the role of individual germline variation in related genes is unknown.

methodsA two-stage candidate pathway association study was conducted among 6983 Chinese women. Stage 1 included 2884 women followed for a median of 5.7 years; Stage 2 included 4099 women followed for a median of 4.0 years. Cox proportional hazards regression was used to estimate the effects of genetic variants on disease-free survival (DFS) and overall survival (OS).

resultsStage 1 included genotyping of 506 variants in 22 genes; analysis was conducted for 370 common variants. Nominally significant associations with DFS and/or OS were found for 20 loci in ten genes in Stage 1; variants in 19 loci were successfully genotyped and evaluated in Stage 2. In analyses of both study stages combined, nominally significant associations were found for nine variants in seven genes; none of these associations surpassed a significance threshold level corrected for the total number of variants evaluated in this study.

conclusionsNo association with survival was found for 370 common variants in 22 angiogenesis and inflammation pathway genes among Chinese women with breast cancer. IMPACT: Our data do not support a large role for common genetic variation in 22 genes in breast cancer prognosis; research on angiogenesis and inflammation genes should focus on common variation in other genes, rare host variants, or tumor alterations.

Indexed as

Breast NeoplasmsChinaFemaleGenetic VariationGenotypeHumansInflammationInflammatory Breast NeoplasmsMiddle AgedNeoplasm StagingNeovascularization, PathologicPolymorphism, Single NucleotideAngiogenesis genesBreast cancer survivalCCL2CCL5CCR2chemokine (C-C motif) ligand 2chemokine (C-C motif) ligand 5chemokine (C-C motif) receptor 2Chinese womenCOL18A1collagen, type XVIII, alpha 1deoxyribonucleic acidDFSdisease-free survivalDNAERestrogen receptorFGFR4fibroblast growth factor receptor 4FLT1fms-related tyrosine kinase 1Genetic variantsHER2HIF1AHPGDhuman epidermal growth factor receptor 2hydroxyprostaglandin dehydrogenasehypoxia inducible factor 1, alpha subunitIL10IL1BIL6Inflammation pathway genesinterleukin 10interleukin 1, betainterleukin 6kbKDRkilobasekinase insert domain receptorMAFmatrix metallopeptidase 1matrix metallopeptidase 13matrix metallopeptidase 2matrix metallopeptidase 3matrix metallopeptidase 7matrix metallopeptidase 9minor allele frequencyMMP1MMP13MMP2MMP3MMP7MMP9OSoverall survivalperiostin, osteoblast specific factorplasminogen activator, urokinasePLAUPOSTNPRprogesterone receptorprostaglandin-endoperoxide synthase 2prostaglandin E synthaseprostaglandin I2 synthasePTGESPTGISPTGS2SBCSSBCSSSERPINE1serpin peptidase inhibitor, clade E, member 1 (previously known as PAI1)Shanghai Breast Cancer StudyShanghai Breast Cancer Survival StudyShanghai Women's Health StudySWHSTGFB1THBS1thrombospondin 1transforming growth factor, beta 1vascular endothelial growth factor AVEGFA

Identifiers

PMID23850146
PMCPMC4064366

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