Inherited DNA-repair gene mutations in African American men with prostate cancer

Oliver Sartor1, Shan Yang2, Elisa Ledet1

  • 1Tulane Cancer Center, Tulane University of School of Medicine, New Orleans, Louisiana, United States.

Oncotarget
|February 18, 2020
PubMed

Insights

African American men with prostate cancer have fewer detected DNA repair gene mutations than Caucasian men. This difference is primarily driven by non-BRCA mutations, highlighting disparities in genetic testing for prostate cancer.

Area of Science:

  • Genetics
  • Oncology
  • Medical Research

Background:

  • Prostate cancer disproportionately affects African American men.
  • Germline DNA repair gene mutations are crucial in prostate cancer development and treatment.
  • Underrepresentation of African Americans in genetic studies limits understanding of mutation prevalence.

Purpose of the Study:

  • To compare the detection rates of pathogenic/likely pathogenic alterations in 14 DNA repair genes between African American and Caucasian men with prostate cancer.
  • To investigate population-specific differences in germline mutation profiles relevant to prostate cancer.

Main Methods:

  • Analysis of a large commercial dataset including African American and Caucasian men with prostate cancer.
  • Evaluation of pathogenic/likely pathogenic alterations in 14 specific DNA repair genes (e.g., BRCA2, BRCA1, ATM, CHEK2).

Main Results:

  • Overall, African American men showed a lower likelihood of detecting pathogenic/likely pathogenic alterations in the 14 DNA repair genes compared to Caucasian men.
  • Germline BRCA mutations had similar detection risks between populations.
  • Non-BRCA DNA repair gene mutations were less common in African Americans.

Conclusions:

  • Significant disparities exist in the detection of DNA repair gene mutations in prostate cancer between African American and Caucasian men.
  • The findings suggest a need for further research into the genetic landscape of prostate cancer in diverse populations.
  • Larger, detailed studies are required to confirm these observations and inform clinical genetic testing strategies.

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