Evidence map›Paper›PMID 32371391›Full record

ArticleThe Journal of biological chemistry2020

The role of the histone H3 variant CENPA in prostate cancer.

Anjan K Saha, Rafael Contreras-Galindo, Yashar S Niknafs, Matthew Iyer, Tingting Qin, Karthik Padmanabhan, Javed Siddiqui, Monica Palande, Claire Wang, Brian Qian and 8 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
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  9. Cryo-EM Analysis of a Unique Subnucleosome Containing Centromere-Specific Histone Variant CENP-A.Genes to cells : devoted to molecular & cellular mechanisms · 2025
    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 2 institutions in 1 country.

Anjan K SahaMedical Scientist Training Program, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0001-6721-1599
Rafael Contreras-GalindoDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-6284-3359
Yashar S NiknafsMedical Scientist Training Program, University of Michigan, Ann Arbor, Michigan, USA.
Matthew IyerMichigan Center for Translational Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Tingting QinDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA.
Karthik PadmanabhanDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-3405-7059
Javed SiddiquiMichigan Center for Translational Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Monica PalandeDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Claire WangDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Brian QianDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Elizabeth WardDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Tara TangDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Scott A TomlinsMichigan Center for Translational Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Scott D GitlinDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Maureen A SartorDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA.
Gilbert S OmennDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Arul M ChinnaiyanProgram in Cancer Biology, University of Michigan, Ann Arbor, Michigan, USA.
David M MarkovitzProgram in Cancer Biology, University of Michigan, Ann Arbor, Michigan, USA dmarkov@umich.edu.
University of Michigan · USHoward Hughes Medical Institute · US

Funding

MICHIGAN MEDICAL SCIENTIST TRAINING PROGRAMT32GM007863 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, KATHLEEN L. · 1985 to 2024
$38.3M
Strategic Vision & Impact on Environmental HealthP30ES017885 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Dana Dolinoy · 2011 to 2026
$21.3M
Integrative epigenomic/genomic profiling and biomarker discovery in HPV+ and HPV-R01CA158286 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROZEK, LAURA, SARTOR, MAUREEN AGNES · 2011 to 2015
$2.6M
DEK Regulation of Hematopoietic Stem Cell Renewal, Fate, and HematopoiesisR01DK109188 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI BROXMEYER, HAL E., MARKOVITZ, DAVID MICHAEL · 2016 to 2019
$2.0M
The Role of Centromeres in the Molecular Biology of Prostate CancerF30CA210379 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SAHA, ANJAN KUMAR · 2016 to 2018
$119k
Discovery and Characterization of an Estrogen Responsive Long Non-Coding RNAF30CA200328 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NIKNAFS, YASHAR SHARIFI · 2016 to 2017
$38k
Howard Hughes Medical InstituteNCI NIH HHS F30 CA200328NCI NIH HHS F30 CA210379NCI NIH HHS R01 CA158286NIDDK NIH HHS R01 DK109188NIEHS NIH HHS P30 ES017885NIGMS NIH HHS T32 GM007863
6 · The paper itself

Abstract

Overexpression of centromeric proteins has been identified in a number of human malignancies, but the functional and mechanistic contributions of these proteins to disease progression have not been characterized. The centromeric histone H3 variant centromere protein A (CENPA) is an epigenetic mark that determines centromere identity. Here, using an array of approaches, including RNA-sequencing and ChIP-sequencing analyses, immunohistochemistry-based tissue microarrays, and various cell biology assays, we demonstrate that CENPA is highly overexpressed in prostate cancer in both tissue and cell lines and that the level of CENPA expression correlates with the disease stage in a large cohort of patients. Gain-of-function and loss-of-function experiments confirmed that CENPA promotes prostate cancer cell line growth. The results from the integrated sequencing experiments suggested a previously unidentified function of CENPA as a transcriptional regulator that modulates expression of critical proliferation, cell-cycle, and centromere/kinetochore genes. Taken together, our findings show that CENPA overexpression is crucial to prostate cancer growth.

Indexed as

Cell Cycle ProteinsCell DivisionCell Line, TumorCell ProliferationCentromere Protein AGain of Function MutationHistonesHumansMaleProstatic NeoplasmsRNA InterferenceRNA, Small InterferingCell Cycle ProteinsCentromere Protein AHistonesRNA, Small Interferingcell proliferationcentromereCentromerecentromere protein A (CENPA)chromatinepigeneticsgene expressiongene regulationhistoneprostate cancertranscription

Identifiers

PMID32371391
PMCPMC7307189
OpenAlexW3023622052

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.