Evidence map›Paper›PMID 17848914›Full record

ArticleBritish journal of cancer2007

Genetic variation in five genes important in telomere biology and risk for breast cancer.

S A Savage, S J Chanock, J Lissowska, L A Brinton, D Richesson, B Peplonska, A Bardin-Mikolajczak, W Zatonski, N Szeszenia-Dabrowska, M Garcia-Closas

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 6 pooled it
2.6field-weighted citation impact, top 11% 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

41 citing papers in PubMed, 6 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Telomere reverse transcriptase (TERT) rs2735940 increases cancer risk.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Pooled it
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  7. Article
  8. Article
  9. Review
  10. Relationship between Telomere Length,International journal of molecular sciences · 2022
    Article
  11. Implications of risk conferred by 5p15.33 loci genetic variants; human telomerase reverse transcriptase rs2736098 and rs2736100 in predisposition of bladder cancer.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2022
    Article
  12. Article
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  14. Association betweenCancer cell international · 2020
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  15. Review
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  17. Oncotarget · 2017
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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

10 authors at 5 institutions in 2 countries.

S A SavageDivision of Cancer Epidemiology and Genetics, Clinical Genetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA. savagesh@mail.nih.gov
S J Chanock
J Lissowska
L A Brinton
D Richesson
B Peplonska
A Bardin-Mikolajczak
W Zatonski
N Szeszenia-Dabrowska
M Garcia-Closas
National Cancer Institute · USThe Maria Sklodowska-Curie National Research Institute of Oncology · PLNofer Institute of Occupational Medicine · PLCenter for Cancer Research · USNational Institutes of Health · US

Funding

HORMONE-RELATED CANCERSZ01CP010126 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI BRINTON, LOUISE · 1996 to 2008
$11.2M
MOLECULAR STUDY OF HOST RESPONSE/GENETIC RISK FACTORS OF INFECTION COMPLICATIONZ01SC010083 · SC · CLINICAL SCIENCES · PI CHANOCK, STEPHEN J · 1997 to 2007
$1.1M
STRUCTURE AND STABILIZATION OF THE BACTERIAL NUCLEOIDZ01DK036120 · NIDDK · DIABETES, DIGESTIVE, KIDNEY DISEASES · PI ZIMMERMAN, STEVEN C. · 1998 to 2005
–
Intramural NIH HHS
6 · The paper itself

Abstract

Telomeres, consisting of TTAGGG nucleotide repeats and a protein complex at chromosome ends, are critical for maintaining chromosomal stability. Genomic instability, following telomere crisis, may contribute to breast cancer pathogenesis. Many genes critical in telomere biology have limited nucleotide diversity, thus, single nucleotide polymorphisms (SNPs) in this pathway could contribute to breast cancer risk. In a population-based study of 1995 breast cancer cases and 2296 controls from Poland, 24 SNPs representing common variation in POT1, TEP1, TERF1, TERF2 and TERT were genotyped. We did not identify any significant associations between individual SNPs or haplotypes and breast cancer risk; however, data suggested that three correlated SNPs in TERT (-1381C>T, -244C>T, and Ex2-659G>A) may be associated with reduced risk of breast cancer among individuals with a family history of breast cancer (odds ratios 0.73, 0.66, and 0.57, 95% confidence intervals 0.53-1.00, 0.46-0.95 and 0.39-0.84, respectively). In conclusion, our data do not support substantial overall associations between SNPs in telomere pathway genes and breast cancer risk. Intriguing associations with variants in TERT among women with a family history of breast cancer warrant follow-up in independent studies.

Indexed as

Genetic VariationPolymorphism, Single NucleotideAdultAgedBreast NeoplasmsCarrier ProteinsCase-Control StudiesDNA, NeoplasmFemaleGenotypeHumansMiddle AgedNuclear ProteinsOdds RatioPolandRisk AssessmentCarrier ProteinsDNA, NeoplasmNuclear ProteinsPOT1 protein, humanRNA-Binding ProteinsShelterin ComplexTATA Box Binding Protein-Like ProteinsTelomeraseTelomere-Binding ProteinsTelomeric Repeat Binding Protein 2TEP1 protein, humanTERF1 protein, humanTERF2 protein, humanTERT protein, human

Identifiers

PMID17848914
PMCPMC2360388
OpenAlexW2085760291

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.