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The Prostate Cancer Androgen Receptor Cistrome in African American Men Associates with Upregulation of Lipid Metabolism and Immune Response.
Berchuck, Jacob E; Adib, Elio; Abou Alaiwi, Sarah; Dash, Amit K; Shin, Jin Na; Lowder, Dallin; McColl, Collin; Castro, Patricia; Carelli, Ryan; Benedetti, Elisa; Deng, Jenny; Robertson, Matthew; Baca, Sylvan C; Bell, Connor; McClure, Heather M; El Zarif, Talal; Davidsohn, Matthew P; Lakshminarayanan, Gitanjali; Rizwan, Kinza; Skapura, Darlene G; Grimm, Sandra L; Davis, Christel M; Ehli, Erik A; Kelleher, Kaitlin M; Seo, Ji-Heui; Mitsiades, Nicholas; Coarfa, Cristian; Pomerantz, Mark M; Loda, Massimo; Ittmann, Michael; Freedman, Matthew L; Kaochar, Salma.
Afiliação
  • Berchuck JE; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Adib E; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Abou Alaiwi S; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Dash AK; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Shin JN; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Lowder D; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • McColl C; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Castro P; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Carelli R; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Benedetti E; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Deng J; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Robertson M; Department of Pathology, Baylor College of Medicine, Houston, Texas.
  • Baca SC; Dan L Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.
  • Bell C; Avera Institute for Human Genetics, Sioux Falls, South Dakota.
  • McClure HM; Avera Institute for Human Genetics, Sioux Falls, South Dakota.
  • El Zarif T; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Davidsohn MP; Dan L Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.
  • Lakshminarayanan G; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Rizwan K; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Skapura DG; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Grimm SL; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Davis CM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Ehli EA; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Kelleher KM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Seo JH; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Mitsiades N; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Coarfa C; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Pomerantz MM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Loda M; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Ittmann M; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Freedman ML; Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Kaochar S; Dan L Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.
Cancer Res ; 82(16): 2848-2859, 2022 08 16.
Article em En | MEDLINE | ID: mdl-35731919
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Receptores Androgênicos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Cancer Res Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Receptores Androgênicos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Cancer Res Ano de publicação: 2022 Tipo de documento: Article