Evidence map›Paper›PMID 35731919›Full record

ArticleCancer research2022

The Prostate Cancer Androgen Receptor Cistrome in African American Men Associates with Upregulation of Lipid Metabolism and Immune Response.

Jacob E Berchuck, Elio Adib, Sarah Abou Alaiwi, Amit K Dash, Jin Na Shin, Dallin Lowder, Collin McColl, Patricia Castro, Ryan Carelli, Elisa Benedetti and 22 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.3field-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

24 citing papers in PubMed, 38 citations in OpenAlex.

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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

32 authors at 6 institutions in 1 country.

Jacob E Berchuck *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-7607-2428
Elio Adib *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-0594-7976
Sarah Abou Alaiwi *Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
Amit K Dash *Department of Medicine, Baylor College of Medicine, Houston, Texas.ORCID 0000-0003-0598-7732
Jin Na ShinDepartment of Medicine, Baylor College of Medicine, Houston, Texas.ORCID 0000-0001-6709-6439
Dallin LowderDepartment of Medicine, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-6679-6051
Collin McCollDepartment of Medicine, Baylor College of Medicine, Houston, Texas.
Patricia CastroDepartment of Pathology, Baylor College of Medicine, Houston, Texas.ORCID 0000-0001-5286-8037
Ryan CarelliAvera Institute for Human Genetics, Sioux Falls, South Dakota.
Elisa BenedettiAvera Institute for Human Genetics, Sioux Falls, South Dakota.ORCID 0000-0003-4616-3860
Jenny DengDepartment of Medicine, Baylor College of Medicine, Houston, Texas.
Matthew RobertsonDan L Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.
Sylvan C BacaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-4087-8606
Connor BellDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Heather M McClureDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-4441-5609
Talal El ZarifDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-4507-2396
Matthew P DavidsohnDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Gitanjali LakshminarayananDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Kinza RizwanDepartment of Medicine, Baylor College of Medicine, Houston, Texas.ORCID 0000-0003-2147-7783
Darlene G SkapuraDepartment of Medicine, Baylor College of Medicine, Houston, Texas.
Sandra L GrimmDan L Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-0682-3134
Christel M DavisDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.ORCID 0000-0003-4973-5035
Erik A EhliDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.ORCID 0000-0002-7865-3015
Kaitlin M KelleherDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-1645-6438
Ji-Heui SeoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-7280-3334
Nicholas MitsiadesDepartment of Medicine, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-4659-476X
Cristian CoarfaDan L Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-4183-4939
Mark M PomerantzDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Massimo LodaAvera Institute for Human Genetics, Sioux Falls, South Dakota.ORCID 0000-0001-9674-8379
Michael IttmannDepartment of Pathology, Baylor College of Medicine, Houston, Texas.
Matthew L Freedman *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-0151-1238
Salma Kaochar *Department of Medicine, Baylor College of Medicine, Houston, Texas.
Baylor College of Medicine · USDana-Farber Cancer Institute · USAvera Health · USBrigham and Women's Hospital · USChildren's Cancer Center · USCornell University · US

Funding

Physician Scientist Training in Cancer ResearchT32CA009172 · NCI · DANA-FARBER CANCER INSTITUTE · PI Jennifer R Brown, James A. DeCaprio · 1985 to 2026
$17.1M
Weill Cornell Medicine (WCM) SPORE in Prostate CancerP50CA211024 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUDAS, LORRAINE J · 2017 to 2021
$10.9M
TRAINING PROGRAM IN CELL AND MOLECULAR BIOLOGYT32GM008231 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI NELSON, DAVID LOREN · 1990 to 2019
$7.2M
THE RNA HELICASE EIF4A IS A THERAPEUTIC VULNERABILITY IN TRIPLE-NEGATIVE BREAST CANCERU54CA233223 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MITSIADES, NICHOLAS · 2018 to 2022
$7.0M
Molecular Link Between Metabolic Syndrome and Prostate CancerR01CA131945 · NCI · DANA-FARBER CANCER INST · PI LODA, MASSIMO · 2008 to 2018
$4.0M
The Clinical Translational Research Certificate of Added Qualification ProgramT32GM136554 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI Melissa Suter, IGNATIA B VAN DEN VEYVER · 2020 to 2026
$3.0M
Targeting Castration Resistant Prostate Cancer via Potent Inhibition of Signaling LipidsR01CA251560 · NCI · BAYLOR COLLEGE OF MEDICINE · PI KAOCHAR, SALMA · 2022 to 2025
$2.4M
NCI NIH HHS P50 CA211024NCI NIH HHS R01 CA131945NCI NIH HHS R01 CA251560NCI NIH HHS T32 CA009172NCI NIH HHS U54 CA233223NIGMS NIH HHS T32 GM008231NIGMS NIH HHS T32 GM136554
6 · The paper itself

Abstract

African-American (AA) men are more likely to be diagnosed with and die from prostate cancer than European American (EA) men. Despite the central role of the androgen receptor (AR) transcription factor in prostate cancer, little is known about the contribution of epigenetics to observed racial disparities. We performed AR chromatin immunoprecipitation sequencing on primary prostate tumors from AA and EA men, finding that sites with greater AR binding intensity in AA relative to EA prostate cancer are enriched for lipid metabolism and immune response genes. Integration with transcriptomic and metabolomic data demonstrated coinciding upregulation of lipid metabolism gene expression and increased lipid levels in AA prostate cancer. In a metastatic prostate cancer cohort, upregulated lipid metabolism associated with poor prognosis. These findings offer the first insights into ancestry-specific differences in the prostate cancer AR cistrome. The data suggest a model whereby increased androgen signaling may contribute to higher levels of lipid metabolism, immune response, and cytokine signaling in AA prostate tumors. Given the association of upregulated lipogenesis with prostate cancer progression, our study provides a plausible biological explanation for the higher incidence and aggressiveness of prostate cancer observed in AA men. SIGNIFICANCE: With immunotherapies and inhibitors of metabolic enzymes in clinical development, the altered lipid metabolism and immune response in African-American men provides potential therapeutic opportunities to attenuate racial disparities in prostate cancer.

Indexed as

Prostatic NeoplasmsReceptors, AndrogenBlack or African AmericanHumansImmunityLipid MetabolismMaleUp-RegulationReceptors, Androgen

Identifiers

PMID35731919
PMCPMC9379363
OpenAlexW4283265713

What OpenQuestion holds

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Registered trials

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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.