Evidence map›Paper›PMID 18575892›Full record

ReviewHuman genetics2008

Hereditary breast cancer: new genetic developments, new therapeutic avenues.

Philippe M Campeau, William D Foulkes, Marc D Tischkowitz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Human genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed, 4 pooled it
6.7field-weighted citation impact, top 3% 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

142 citing papers in PubMed, 4 syntheses or guidelines pooled it, 323 citations in OpenAlex.

  1. Pooled it
  2. Genetic tests to identify risk for breast cancer.Seminars in oncology nursing · 2015
    Pooled it
  3. Ethnicity modifies the association between functional microRNA polymorphisms and breast cancer risk: a HuGE meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
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82 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Philippe M CampeauDepartment of Medical Genetics, McGill University Health Centre, McGill University, Montreal, QC, Canada. philippe.campeau@mail.mcgill.ca
William D Foulkes
Marc D Tischkowitz
McGill University Health Centre · CAJewish General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Six genes confer a high risk for developing breast cancer (BRCA1/2, TP53, PTEN, STK11, CDH1). Both BRCA1 and BRCA2 have DNA repair functions, and BRCA1/2 deficient tumors are now being targeted by poly(ADP-ribose) polymerase inhibitors. Other genes conferring an increased risk for breast cancer include ATM, CHEK2, PALB2, BRIP1 and genome-wide association studies have identified lower penetrance alleles including FGFR2, a minor allele of which is associated with breast cancer. We review recent findings related to the function of some of these genes, and discuss how they can be targeted by various drugs. Gaining deeper insights in breast cancer susceptibility will improve our ability to identify those families at increased risk and permit the development of new and more specific therapeutic approaches.

Indexed as

Acid Anhydride HydrolasesAMP-Activated Protein Kinase KinasesAnimalsAntigens, CDAtaxia Telangiectasia Mutated ProteinsBreast NeoplasmsCadherinsCell Cycle ProteinsCheckpoint Kinase 2DNA-Binding ProteinsDNA Repair EnzymesFanconi Anemia Complementation Group N ProteinFanconi Anemia Complementation Group ProteinsGenes, BRCA1Genes, BRCA2Genes, p53Acid Anhydride HydrolasesAMP-Activated Protein Kinase KinasesAntigens, CDAtaxia Telangiectasia Mutated ProteinsATM protein, humanBRIP1 protein, humanCadherinsCDH1 protein, humanCell Cycle ProteinsCheckpoint Kinase 2CHEK2 protein, humanDNA-Binding ProteinsDNA Repair EnzymesFanconi Anemia Complementation Group N ProteinFanconi Anemia Complementation Group ProteinsNBN protein, humanNuclear ProteinsPALB2 protein, humanProtein Serine-Threonine KinasesPTEN PhosphohydrolasePTEN protein, humanRAD50 protein, humanRNA HelicasesSTK11 protein, humanTumor Suppressor Proteins

Identifiers

PMID18575892
OpenAlexW2115773111

What OpenQuestion holds

Textmetadata
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.