An Inherited Heteroplasmic Mutation in Mitochondrial Gene COI in a Patient with Prostate Cancer Alters Reactive Oxygen, Reactive Nitrogen and Proliferation

Author:

Arnold Rebecca S.12,Sun Qian1,Sun Carrie Q.1,Richards Jendai C.1,O'Hearn Sean3,Osunkoya Adeboye O.1245,Wallace Douglas C.367,Petros John A.1245

Affiliation:

1. Department of Urology, School of Medicine, Emory University, 1365 Clifton Rd. Building B, Atlanta, GA 30322, USA

2. Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA

3. Center for Molecular and Mitochondrial Medicine and Genetics (MAMMAG), University of California Irvine, Irvine, CA 92697, USA

4. Department of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30322, USA

5. Department of Urology, The Atlanta VA Medical Center, Decatur, GA 30033, USA

6. Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA

7. Department of Pathology, University of Pennsylvania, Philadelphia, PA 19104, USA

Abstract

Mitochondrial DNA (mtDNA) mutations have been found in many cancers but the physiological derangements caused by such mutations have remained elusive. Prostate cancer is associated with both inherited and somatic mutations in the cytochrome c oxidase (COI) gene. We present a prostate cancer patient-derived rare heteroplasmic mutation of this gene, part of mitochondrial respiratory complex IV. Functional studies indicate that this mutation leads to the simultaneous decrease in cytochrome oxidation, increase in reactive oxygen, and increased reactive nitrogen. These data suggest that mitochondrial DNA mutations resulting in increased reactive oxygen and reactive nitrogen generation may be involved in prostate cancer biology.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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