Evidence map›Paper›PMID 19500394›Full record

ArticleBMC cancer2009

Genetic variants in FGFR2 and FGFR4 genes and skin cancer risk in the Nurses' Health Study.

Hongmei Nan, Abrar A Qureshi, David J Hunter, Jiali Han

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  7. Review
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  9. Determination ofDisease markers · 2019
    Article
  10. Article
  11. Contribution of glutathione S-transferase gene polymorphisms to development of skin cancer.International journal of clinical and experimental medicine · 2015
    Article
  12. Review
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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

4 authors at 2 institutions in 1 country.

Hongmei NanProgram in Molecular and Genetic Epidemiology, Department of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA. hnan@hsph.harvard.edu
Abrar A Qureshi
David J Hunter
Jiali Han
Brigham and Women's Hospital · USHarvard University · US

Funding

Cohort Study of Genetic Susceptibility to Cutaneous Malignant MelanomaR01CA122838 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI HAN, JIALI · 2008 to 2010
$1.4M
Genetic Variants in Immunological Mediator Genes and Skin Cancer RiskR03CA132175 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI HAN, JIALI · 2007 to 2008
$174k
NCI NIH HHS CA122838NCI NIH HHS CA132175
6 · The paper itself

Abstract

backgroundThe human fibroblast growth factor (FGF) and its receptor (FGFR) play an important role in tumorigenesis. Deregulation of the FGFR2 gene has been identified in a number of cancer sites. Overexpression of the FGFR4 protein has been linked to cutaneous melanoma progression. Previous studies reported associations between genetic variants in the FGFR2 and FGFR4 genes and development of various cancers.

methodsWe evaluated the associations of four genetic variants in the FGFR2 gene highly related to breast cancer risk and the three common tag-SNPs in the FGFR4 gene with skin cancer risk in a nested case-control study of Caucasians within the Nurses' Health Study (NHS) among 218 melanoma cases, 285 squamous cell carcinoma (SCC) cases, 300 basal cell carcinoma (BCC) cases, and 870 controls.

resultsWe found no evidence for associations between these seven genetic variants and the risks of melanoma and nonmelanocytic skin cancer.

conclusionGiven the power of this study, we did not detect any contribution of genetic variants in the FGFR2 or FGFR4 genes to inherited predisposition to skin cancer among Caucasian women.

Indexed as

AdultAgedBasal Cell CarcinomaCarcinoma, Squamous CellFemaleGenetic Predisposition to DiseaseHumansMelanomaMiddle AgedPolymorphism, Single NucleotideReceptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 4Skin NeoplasmsFGFR2 protein, humanFGFR4 protein, humanReceptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 4

Identifiers

PMID19500394
PMCPMC2699349
OpenAlexW2108728470

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.