Evidence map›Paper›PMID 20051372›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2010

Altered gene expression in morphologically normal epithelial cells from heterozygous carriers of BRCA1 or BRCA2 mutations.

Alfonso Bellacosa, Andrew K Godwin, Suraj Peri, Karthik Devarajan, Elena Caretti, Lisa Vanderveer, Betsy Bove, Carolyn Slater, Yan Zhou, Mary Daly and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  6. iPSC-Derived Hereditary Breast Cancer Model Reveals theInternational journal of molecular sciences · 2021
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  11. Article
  12. Article
  13. Cancer management and research · 2018
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 3 institutions in 1 country.

Alfonso BellacosaFox Chase Cancer Center, Philadelphia, PA 19111, USA. Alfonso.Bellacosa@fccc.edu
Andrew K Godwin
Suraj Peri
Karthik Devarajan
Elena Caretti
Lisa Vanderveer
Betsy Bove
Carolyn Slater
Yan Zhou
Mary Daly
Sharon Howard
Kerry S Campbell
Emmanuelle Nicolas
Anthony T Yeung
Margie L Clapper
James A Crowell
Henry T Lynch
Eric Ross
Levy Kopelovich
Alfred G Knudson
Creighton University · USNational Cancer Institute · USFox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Therapeutic Micro RNA Strategies for Ovarian CancerP50CA083638 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GODWIN, ANDREW K., GOLEMIS, ERICA A. · 1999 to 2013
$33.6M
The MED1 Protein in DNA Damage Response and RepairR01CA078412 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI BELLACOSA, ALFONSO · 2004 to 2014
$3.7M
PHASE I STUDIES OF CHEMOPREVENTIVE AGENTS, WORKSTATEMENTN01CN095037 · CN · FOX CHASE CANCER CENTER · PI KNUDSON, ALFRED G · 1999 to 2000
$975k
PHASE I STUDIES OF CHEMOPREVENTIVE AGENTS, WORKSTATEMENT 37-261995037N01CA095037 · NCI · FOX CHASE CANCER CENTER · 2002 to 2002
–
NEW APPROACHES TO ANALYSIS OF BIOPOLYMERSR01CA043309 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI VARSHAVSKY, ALEXANDER J · 1986 to 1990
–
NCI NIH HHS N01 CN043309NCI NIH HHS N01 CN095037NCI NIH HHS N01-CN-43309NCI NIH HHS N01 CN-95037NCI NIH HHS P30 CA006927NCI NIH HHS P30 CA06927NCI NIH HHS P50 CA083638NCI NIH HHS R01 CA078412
6 · The paper itself

Abstract

We hypothesized that cells bearing a single inherited "hit" in a tumor suppressor gene express an altered mRNA repertoire that may identify targets for measures that could delay or even prevent progression to carcinoma. We report here on the transcriptomes of primary breast and ovarian epithelial cells cultured from BRCA1 and BRCA2 mutation carriers and controls. Our comparison analyses identified multiple changes in gene expression, in both tissues for both mutations, which were validated independently by real-time reverse transcription-PCR analysis. Several of the differentially expressed genes had been previously proposed as cancer markers, including mammaglobin in breast cancer and serum amyloid in ovarian cancer. These findings show that heterozygosity for a mutant tumor suppressor gene can alter the expression profiles of phenotypically normal epithelial cells in a gene-specific manner; these detectable effects of "one hit" represent early molecular changes in tumorigenesis that may serve as novel biomarkers of cancer risk and as targets for chemoprevention.

Indexed as

Gene Expression ProfilingGenes, BRCA1Genes, BRCA2Genetic Predisposition to DiseaseBiomarkers, TumorBreastData MiningEpithelial CellsFemaleGene ExpressionHeterozygoteHumansMutationOligonucleotide Array Sequence AnalysisOvaryReverse Transcriptase Polymerase Chain ReactionBiomarkers, TumorRNA, Messenger

Identifiers

PMID20051372
PMCPMC2804937
OpenAlexW2096813217

What OpenQuestion holds

Textmetadata
LicenceTDM
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.