Evidence map›Paper›PMID 18563556›Full record

ArticleBreast cancer research and treatment2009

Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors.

Anita L Bane, Dushanthi Pinnaduwage, Sarah Colby, Michael Reedijk, Sean E Egan, Shelley B Bull, Frances P O'Malley, Irene L Andrulis

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 56 citations in OpenAlex.

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  7. Fibroblast Growth Factor Receptor 2 Signaling in Breast Cancer.International journal of biological sciences · 2017
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  19. Pathology of hereditary breast cancer.Cellular oncology (Dordrecht, Netherlands) · 2011
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  20. Phenotype-genotype correlation in familial breast cancer.Journal of mammary gland biology and neoplasia · 2011
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4 · The record

Corrections and comments

  • Erratum issued
    Reedijk, Michael [added]; Egan, Sean E [added]
5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Anita L BaneDepartment of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada.
Dushanthi Pinnaduwage
Sarah Colby
Michael Reedijk
Sean E Egan
Shelley B Bull
Frances P O'Malley
Irene L Andrulis
Lunenfeld-Tanenbaum Research Institute · CAMount Sinai Hospital · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBRCA1- and BRCA2-associated tumors appear to have distinct molecular signatures. BRCA1-associated tumors are predominantly basal-like cancers, whereas BRCA2-associated tumors have a predominant luminal-like phenotype. These two molecular signatures reflect in part the two cell types found in the terminal duct lobular unit of the breast. To elucidate novel genes involved in these two spectra of breast tumorigenesis we performed global gene expression analysis on breast tumors from germline BRCA1 and BRCA2 mutation carriers. METHODOLOGY: Breast tumor RNAs from 7 BRCA1 and 6 BRCA2 mutation carriers were profiled using UHN human 19K cDNA microarrays. Supervised univariate analyses were conducted to identify genes differentially expressed between BRCA1 and BRCA2-associated tumors. Selected discriminatory genes were validated using real time reverse transcription polymerase chain reaction in the tumor RNAs, and/or by immunohistochemistry (IHC) or by in situ hybridization (ISH) on tissue microarrays (TMAs) containing an independent set of 58 BRCA1 and 64 BRCA2-associated tumors.

resultsGenes more highly expressed in BRCA1-associated tumors included stathmin, osteopontin, TGFbeta2 and Jagged 1 in addition to genes previously identified as characteristic of basal-like breast cancers. BRCA2-associated cancers were characterized by the higher relative expression of FGF1 and FGFR2. FGFR2 protein was also more highly expressed in BRCA2-associated cancers (P = 0.004). SIGNIFICANCE: BRCA1-associated tumours demonstrated increased expression of component genes of the Notch and TGFbeta pathways whereas the higher expression of FGFR2 and FGF1 in BRCA2-associated cancers suggests the existence of an autocrine stimulatory loop.

Indexed as

Gene Expression ProfilingGenes, BRCA2Genetic Predisposition to DiseaseBiomarkers, TumorBreast NeoplasmsCalcium-Binding ProteinsFemaleFibroblast Growth Factor 1Gene ExpressionGenes, BRCA1HumansImmunohistochemistryIn Situ HybridizationIntercellular Signaling Peptides and ProteinsJagged-1 ProteinMembrane ProteinsBiomarkers, TumorCalcium-Binding ProteinsFGFR2 protein, humanFibroblast Growth Factor 1Intercellular Signaling Peptides and ProteinsJAG1 protein, humanJagged-1 ProteinMembrane ProteinsOsteopontinReceptor, Fibroblast Growth Factor, Type 2Receptors, NotchRNA, MessengerSerrate-Jagged ProteinsStathminTGFB2 protein, humanTransforming Growth Factor beta2

Identifiers

PMID18563556
PMCPMC2727582
OpenAlexW2014331129

What OpenQuestion holds

Textmetadata
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Registered trials

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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.