Commentary 10.1172/JCI128707
1Barbara Ann Karmanos Cancer Institute, Population Studies and Disparities Research, Wayne State University, Detroit, Michigan, USA.
2Department of Medicine, Duke Cancer Institute, Duke University, Durham, North Carolina, USA.
Address correspondence to: Jennifer L. Beebe-Dimmer, Wayne State University, Barbara Ann Karmanos Cancer Institute, Program Leader Population Studies and Disparities Research, 4100 John R, Detroit, Michigan, 48201, USA. Phone: 313.578.4209; Email: dimmerj@karmanos.org. Or to: Kathleen A. Cooney, Duke University School of Medicine, 2301 Erwin Road, Suite 1102, Durham, North Carolina, 27710, USA. Phone: 919.681.2452; Email: kathleen.cooney@duke.edu.
Find articles by Beebe-Dimmer, J. in: JCI | PubMed | Google Scholar
1Barbara Ann Karmanos Cancer Institute, Population Studies and Disparities Research, Wayne State University, Detroit, Michigan, USA.
2Department of Medicine, Duke Cancer Institute, Duke University, Durham, North Carolina, USA.
Address correspondence to: Jennifer L. Beebe-Dimmer, Wayne State University, Barbara Ann Karmanos Cancer Institute, Program Leader Population Studies and Disparities Research, 4100 John R, Detroit, Michigan, 48201, USA. Phone: 313.578.4209; Email: dimmerj@karmanos.org. Or to: Kathleen A. Cooney, Duke University School of Medicine, 2301 Erwin Road, Suite 1102, Durham, North Carolina, 27710, USA. Phone: 919.681.2452; Email: kathleen.cooney@duke.edu.
Find articles by Cooney, K. in: JCI | PubMed | Google Scholar
First published May 6, 2019 - More info
African Americans are at increased risk of cancer and associated mortalities compared with European American populations. Socioeconomic, cultural, and biological factors have been implicated in this discrepancy. In this issue of the JCI, Piyarathna et al. identify a set of genes that are upregulated in a number of tumor types in African American cancer patients as compared with European American patients. These genes were associated with enhanced oxidative phosphorylation and upregulation of transcription factors that promote mitochondrial biogenesis, resulting in greater numbers of mitochondria in tumor samples from African American subjects. Together, these results indicate that mitochondria dysfunction may underlie the increased cancer incidence and poor outcomes observed in African American patients.
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