Evidence map›Paper›PMID 34193566›Full record

ArticleJournal for immunotherapy of cancer2021

TGM4: an immunogenic prostate-restricted antigen.

Zoila A Lopez-Bujanda, Aleksandar Obradovic, Thomas R Nirschl, Laura Crowley, Rodney Macedo, Alexandros Papachristodoulou, Timothy O'Donnell, Uri Laserson, Jelani C Zarif, Ran Reshef and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2021. 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
2.2field-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

17 citing papers in PubMed, 24 citations in OpenAlex.

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  16. Biochemical Characterisation of Human Transglutaminase 4.International journal of molecular sciences · 2021
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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 1 country.

Zoila A Lopez-BujandaDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0001-5729-7309
Aleksandar ObradovicColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0002-8009-0186
Thomas R NirschlDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-3329-6229
Laura CrowleyDepartment of Genetics and Development, Columbia University Irving Medical Center, New York, New York, USA.
Rodney MacedoColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0001-6252-7703
Alexandros PapachristodoulouHerbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0001-8488-7785
Timothy O'DonnellDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Uri LasersonDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0002-8429-7686
Jelani C ZarifBloomberg~Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.
Ran ReshefColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0003-2185-9546
Tiezheng YuanDivision of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Mithil K SoniColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, New York, USA.
Emmanuel S AntonarakisDepartment of Oncology, Johns Hopkins Medicine Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.ORCID 0000-0003-0031-9655
Michael C HaffnerDivisions of Human Biology and Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.ORCID 0000-0003-0809-6425
H Benjamin LarmanDivision of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Michael M ShenDepartment of Genetics and Development, Columbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0002-4042-1657
Pawel MuranskiColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0002-4446-6385
Charles G DrakeColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, New York, USA cgd2139@cumc.columbia.edu.ORCID 0000-0001-9610-3677
Columbia University Irving Medical Center · USBloomberg (United States) · USJohns Hopkins University · USIcahn School of Medicine at Mount Sinai · USFred Hutch Cancer Center · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Parisa Tehranifar · 1985 to 2026
$115.3M
Analysis of epithelial heterogeneity in prostate development and cancerR01CA238005 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHEN, MICHAEL M. · 2019 to 2023
$2.1M
Analysis of Lag-3 in Regulatory T Cell Function and Immune SupressionR01CA127153 · NCI · JOHNS HOPKINS UNIVERSITY · PI DRAKE, CHARLES G. · 2008 to 2012
$1.7M
Targeting M2-Tumor Associated Macrophages to overcome tumor immunity in metastatic castration-resistant prostate cancerK22CA237623 · NCI · JOHNS HOPKINS UNIVERSITY · PI ZARIF, JELANI CHINELO · 2019 to 2021
$461k
NCI NIH HHS K22 CA237623NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA013696NCI NIH HHS R01 CA127153NCI NIH HHS R01 CA238005
6 · The paper itself

Abstract

backgroundProstate cancer is the second leading cause of cancer-related death in men in the USA; death occurs when patients progress to metastatic castration-resistant prostate cancer (CRPC). Although immunotherapy with the Food and Drug Administration-approved vaccine sipuleucel-T, which targets prostatic acid phosphatase (PAP), extends survival for 2-4 months, the identification of new immunogenic tumor-associated antigens (TAAs) continues to be an unmet need.

methodsWe evaluated the differential expression profile of castration-resistant prostate epithelial cells that give rise to CRPC from mice following an androgen deprivation/repletion cycle. The expression levels of a set of androgen-responsive genes were further evaluated in prostate, brain, colon, liver, lung, skin, kidney, and salivary gland from murine and human databases. The expression of a novel prostate-restricted TAA was then validated by immunostaining of mouse tissues and analyzed in primary tumors across all human cancer types in The Cancer Genome Atlas. Finally, the immunogenicity of this TAA was evaluated in vitro and in vivo using autologous coculture assays with cells from healthy donors as well as by measuring antigen-specific antibodies in sera from patients with prostate cancer (PCa) from a neoadjuvant clinical trial.

resultsWe identified a set of androgen-responsive genes that could serve as potential TAAs for PCa. In particular, we found transglutaminase 4 (Tgm4) to be highly expressed in prostate tumors that originate from luminal epithelial cells and only expressed at low levels in most extraprostatic tissues evaluated. Furthermore, elevated levels of

conclusionsThese results suggest that TGM4 is an immunogenic, prostate-restricted antigen with the potential for further development as an immunotherapy target.

Indexed as

AnimalsHumansImmunotherapyMaleMiceProstateTransglutaminasestransglutaminase 4Transglutaminasesantigensimmunogenicityprostatic neoplasmsvaccine

Identifiers

PMID34193566
PMCPMC8246381
OpenAlexW3175249622

What OpenQuestion holds

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LicenceCC BY-NC
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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.