Evidence map›Paper›PMID 21453513›Full record

ArticleJournal of translational medicine2011

Tumor escape and progression of HER-2/neu negative breast cancer under immune pressure.

Maciej Kmieciak, Kyle K Payne, Michael O Idowu, Margaret M Grimes, Laura Graham, Maria-Libera Ascierto, Ena Wang, Xiang-Yang Wang, Harry D Bear, Masoud H Manjili

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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  11. An immunologic portrait of cancer.Journal of translational medicine · 2011
    Review
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 2 institutions in 1 country.

Maciej KmieciakDepartment of Microbiology & Immunology, Virginia Commonwealth University Massey Cancer Center, Richmond, 23298, USA.
Kyle K Payne
Michael O Idowu
Margaret M Grimes
Laura Graham
Maria-Libera Ascierto
Ena Wang
Xiang-Yang Wang
Harry D Bear
Masoud H Manjili
Virginia Commonwealth University · USNational Institutes of Health Clinical Center · US

Funding

Large Stress Proteins in Biology and MedicineR01CA154708 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2011 to 2015
$1.5M
Scavenger Receptor-A and Immune RegulationR01CA129111 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2007 to 2011
$1.2M
Enhancement of HER-2/neu-based therapy using HSP110R01CA104757 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI MANJILI, MASOUD H. · 2005 to 2008
$912k
NCI NIH HHS R01 CA104757NCI NIH HHS R01 CA129111NCI NIH HHS R01 CA154708
6 · The paper itself

Abstract

backgroundEmerging data from pre-clinical and clinical studies suggest that HER-2/neu-specific T cell responses could induce HER-2/neu antigen loss in the tumor cells. These data suggest that patients with HER-2/neu negative breast cancer might have had HER-2/neu positive premalignant lesions in the past that progressed to HER-2/neu negative breast cancer under HER-2/neu-specific immune pressure.

methodsWe conducted a pilot study in patients with HER-2/neu positive and HER-2/neu negative breast cancers as well as a patient with ductal carcinoma in situ (DCIS). HER-2/neu expression was determined by FISH. HER-2/neu-specific T cell responses were determined by using IFN-γ ELISA. Expression of IFN-γ Rα in the tumors was determined by immunohistochemistry analysis of paraffin-embedded tissues.

resultsWe determined that majority of (10 of 12) patients with HER-2/neu negative breast cancer had HER-2/neu-specific IFN-γ producing T cell responses which was stronger than those in patients with HER-2/neu positive tumors. Such immune responses were associated with nuclear translocation of IFN-γ Rα in their tumor cells. Patient with DCIS also showed HER-2/neu-specific T cell responses.

conclusionThese data suggest that conducting retrospective studies in patients with HER-2/neu negative breast cancers and prospective studies in patients with HER-2/neu positive DCIS can determine whether HER-2/neu negative invasive carcinomas arise from HER-2/neu positive DCIS under the immune pressure.

Indexed as

Disease ProgressionBreast NeoplasmsCell Line, TumorCell NucleusErb-b2 Receptor Tyrosine KinasesFemaleHumansInterferon-gammaInterferon gamma ReceptorProtein TransportReceptors, InterferonT-LymphocytesTumor EscapeERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesInterferon-gammaInterferon gamma ReceptorReceptors, Interferon

Identifiers

PMID21453513
PMCPMC3076247
OpenAlexW2163931403

What OpenQuestion holds

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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.