Evidence map›Paper›PMID 19737960›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2009

Identification of the transcription factor single-minded homologue 2 as a potential biomarker and immunotherapy target in prostate cancer.

Mohamed S Arredouani, Bin Lu, Manoj Bhasin, Miriam Eljanne, Wen Yue, Juan-Miguel Mosquera, Glenn J Bubley, Vivian Li, Mark A Rubin, Towia A Libermann and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 25% 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

120 citing papers in PubMed, 1 synthesis or guideline pooled it, 188 citations in OpenAlex.

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60 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

11 authors at 3 institutions in 1 country.

Mohamed S ArredouaniDivision of Urology, Department of Surgery, Genomics Center, and Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
Bin Lu
Manoj Bhasin
Miriam Eljanne
Wen Yue
Juan-Miguel Mosquera
Glenn J Bubley
Vivian Li
Mark A Rubin
Towia A Libermann
Martin G Sanda
Cornell University · USHarvard University · USBeth Israel Deaconess Medical Center · US

Funding

Prostate Cancer Biomarker and Imaging Validation Alliance: Emory University, University of Alabama Birmingham, and University of Texas SouthwesternU01CA113913 · NCI · EMORY UNIVERSITY · PI Martin G. Sanda · 2005 to 2026
$16.4M
MODULATING TOLERANCE FOR PROSTATE CANCER ANTIGEN VACCINER01CA082419 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANDA, MARTIN G · 2000 to 2003
$1.1M
NCI NIH HHS R01 CA082419NCI NIH HHS U01 CA113913NCI NIH HHS U01-CA113913
6 · The paper itself

Abstract

purposeIdentification of novel biomarkers and immunotherapy targets for prostate cancer (PCa) is crucial to better diagnosis and therapy. We sought to identify novel PCa tumor-associated antigens (TAA) that are expressed in PCa, absent in nonprostate human tissue, and immunogenic for immune responses restricted by human HLA. EXPERIMENTAL DESIGN AND

resultsUsing microarray analysis of normal and cancerous human prostate tissues, we identified 1,063 genes overexpressed in PCa. After validating 195 transcripts in publicly available array data sets, we interrogated expression of these TAAs in normal human tissues to identify genes that are not expressed at detectable levels in normal, nonprostate adult human tissue. We identified 23 PCa TAA candidates. Real-time PCR confirmed that 15 of these genes were overexpressed in PCa (P< 0.05 for each). The most frequently overexpressed gene, single-minded homologue 2 (SIM2), was selected for further evaluation as a potential target for immunotherapy. ELISA assay revealed that a fraction of PCa patients exhibited immune responsiveness to SIM2 as evidenced by the presence of autoantibodies to SIM2 in their sera. We next showed binding of putative HLA-A2.1-restricted SIM2 epitopes to human A2.1, and immunization of transgenic HLA-A2.1 mice showed induction of SIM2-specific CTL responses in vivo.

conclusionsOur findings that SIM2 is selectively expressed in PCa, that human HLA-A2.1-restricted SIM2 epitopes induce specific T cells in vivo, and that anti-SIM2 antibodies are detectable in PCa patients' sera implicate SIM2 as a PCa-associated antigen that is a suitable potential target for PCa immunotherapy.

Indexed as

ImmunotherapyAdultAnimalsBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCell Line, TumorEnzyme-Linked Immunosorbent AssayGene Expression ProfilingHumansMaleMiceMice, TransgenicOligonucleotide Array Sequence AnalysisProstatic NeoplasmsReverse Transcriptase Polymerase Chain ReactionBasic Helix-Loop-Helix ProteinsBiomarkers, TumorSIM2 protein, human

Identifiers

PMID19737960
PMCPMC5573151
OpenAlexW2159126410

What OpenQuestion holds

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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.