Evidence map›Paper›PMID 20924104›Full record

ArticleCancer research2010

Receptor tyrosine kinase signaling favors a protumorigenic state in breast cancer cells by inhibiting the adaptive immune response.

Josie Ursini-Siegel, Sean Cory, Dongmei Zuo, William R Hardy, Elton Rexhepaj, Sonya Lam, Babette Schade, Karin Jirstrom, Eva Bjur, Ciriaco A Piccirillo and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Receptor tyrosine kinase inhibitors in cancer.Cellular and molecular life sciences : CMLS · 2023
    Review
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Review
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  10. The immune microenvironment of breast ductal carcinoma in situ.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2016
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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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

18 authors at 5 institutions in 3 countries.

Josie Ursini-SiegelGoodman Cancer Centre and Department of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Sean Cory
Dongmei Zuo
William R Hardy
Elton Rexhepaj
Sonya Lam
Babette Schade
Karin Jirstrom
Eva Bjur
Ciriaco A Piccirillo
David Denardo
Lisa M Coussens
Donal J Brennan
William M Gallagher
Morag Park
Tony Pawson
Michael Hallett
William J Muller
Lund University · SELunenfeld-Tanenbaum Research Institute · CAUniversity College Dublin · IEMount Sinai Hospital · CAMcGill University · CA

Funding

Regulation of Inflammation-Associated Epithelial Cancer DevelopmentR01CA130980 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COUSSENS, LISA M. · 2008 to 2012
$1.6M
Improved Drug Delivery to Tumors Using Novel Tissue Perfusion ApproachesR01CA140943 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOUDREAU, NANCY JOAN, COUSSENS, LISA M. · 2009 to 2012
$1.0M
CIHRNCI NIH HHS R01 CA130980NCI NIH HHS R01 CA140943
6 · The paper itself

Abstract

Using transgenic mouse models of breast cancer that ablate Src homology and collagen A (ShcA) expression or oncogene-coupled ShcA signaling, we previously showed that this adaptor is critical for mammary tumor onset and progression. We now provide the first evidence that ShcA regulates mammary tumorigenesis, in part, through its ability to regulate the adaptive immune response. Inactivation of ShcA signaling within tumor cells results in extensive CD4(+) T-cell infiltration and induction of a humoral immune response in mammary tumors. This is associated with a robust CTL response in preneoplastic lesions that are deficient in ShcA signaling. Moreover, mammary tumor progression of ShcA-deficient hyperplasias is accelerated in a T cell-deficient background. We also uncover a clinically relevant correlation between high ShcA expression and low CTL infiltration in human breast cancers. Finally, we define a novel ShcA-regulated immune signature that functions as an independent prognostic marker of survival in human epidermal growth factor receptor 2(+) and basal breast cancers. We reveal a novel role for tumor cell-derived ShcA in the establishment and maintenance of an immunosuppressive state.

Indexed as

AnimalsBreast NeoplasmsCD4-Positive T-LymphocytesFemaleHumansImmunosuppression TherapyMammary Neoplasms, ExperimentalMiceMice, TransgenicOligonucleotide Array Sequence AnalysisParityPregnancyProportional Hazards ModelsReceptor Protein-Tyrosine KinasesRNA, NeoplasmShc Signaling Adaptor ProteinsReceptor Protein-Tyrosine KinasesRNA, NeoplasmShc Signaling Adaptor Proteins

Identifiers

PMID20924104
PMCPMC3660232
OpenAlexW2135655765

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.