Revisiting HER2 in Prostate Cancer from an Inclusive Perspective: From Biomarkers to Omics.

Black men ERBB2 HER2 genetic ancestry omics prostate cancer

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
25 Sep 2024
Historique:
received: 17 07 2024
revised: 18 09 2024
accepted: 19 09 2024
medline: 16 10 2024
pubmed: 16 10 2024
entrez: 16 10 2024
Statut: epublish

Résumé

Human epidermal growth factor receptor 2 (HER2) is a major driver of disease progression, treatment resistance, and worse survival for patients with various types of cancers, including prostate cancer. However, key bench studies and clinical trials have failed to evaluate the role of HER2 in prostate cancer using racially diverse experimental designs and protocols. This lack of diversity represents what has been the status quo of cancer research in the United States for decades. In the case of prostate cancer, homogenic study designs are problematic as Black men are much more likely to be diagnosed and die from aggressive and incurable forms of the disease. Therefore, the strategic inclusion of biospecimens collected from Black patients as well as the recruitment and enrollment of Black men into prostate cancer clinical trials is necessary to comprehensively evaluate genetic and molecular factors that contribute to variable outcomes in this high-risk population. Additionally, a higher prevalence of HER2 expression in Black men was recently reported in a small cohort of prostate cancer patients and may contribute to worsened prognosis. In this review, we carefully consider the role of HER2 in prostate cancer while, for the first time, taking into account the influences of race and genetic ancestry.

Identifiants

pubmed: 39409883
pii: cancers16193262
doi: 10.3390/cancers16193262
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : NIH HHS
ID : TL1TR002382
Pays : United States
Organisme : NIH HHS
ID : UL1 TR002378
Pays : United States
Organisme : NIH/NIGMS
ID : R25GM058268
Organisme : NIH/NCI
ID : U54CA118638
Organisme : Chan Zuckerberg Initiative
ID : Accelerate Precision Health
Organisme : NIH HHS
ID : 1R01GM112490
Pays : United States
Organisme : NIH HHS
ID : 1R01GM130091
Pays : United States
Organisme : NIH HHS
ID : 1U01CA225753
Pays : United States
Organisme : Robert A. Welch Foundation
ID : D-0005
Organisme : NIH HHS
ID : KL2TR002381
Pays : United States
Organisme : Department of Defense Prostate Cancer Research Program
ID : W81XWH2110038
Organisme : Prostate Cancer Foundation
ID : 20YOUN04
Organisme : NIH/NIMHD
ID : 2U54MD007602

Auteurs

Nicole Mavingire (N)

Department of Surgery, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Janelle C Moore (JC)

Department of Surgery, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Jabril R Johnson (JR)

Department of Microbiology, Biochemistry, & Immunology, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Abdulrahman M Dwead (AM)

Department of Surgery, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Cheryl D Cropp (CD)

Department of Pharmacology & Toxicology, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Yehia Mechref (Y)

Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA.

Firas Kobeissy (F)

Department of Neurobiology, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Soroush Rais-Bahrami (S)

Department of Urology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35294, USA.
Department of Radiology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35294, USA.
O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35294, USA.

Leanne Woods-Burnham (L)

Department of Surgery, Morehouse School of Medicine, Atlanta, GA 30310, USA.

Classifications MeSH