Mitochondrial DNA, nuclear context, and the risk for carcinogenesis

Author:

Kaufman Brett A.1,Picard Martin234,Sondheimer Neal56ORCID

Affiliation:

1. Center for Metabolism and Mitochondrial Medicine, Division of CardiologyVascular Medicine Institute, Department of Medicine, University of Pittsburgh Medical SchoolPittsburgh Pennsylvania

2. Department of Psychiatry, Division of Behavioral MedicineColumbia University Medical CenterNew York New York

3. Department of Neurology, H. Houston Merritt Center, Columbia Translational Neuroscience InitiativeColumbia University Medical CenterNew York New York

4. Columbia Aging Center, Columbia University Mailman School of Public HealthNew York New York

5. Division of Clinical and Metabolic GeneticsThe Hospital for Sick ChildrenToronto OntarioM5G1X8 Canada

6. Department of PaediatricsThe University of Toronto School of MedicineToronto OntarioM5G1X8 Canada

Funder

National Institutes of Health

March of Dimes

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Genetics(clinical),Epidemiology

Reference66 articles.

1. Perinuclear mitochondrial clustering creates an oxidant‐rich nuclear domain required for hypoxia‐induced transcription;Al‐Mehdi AB;Sci Signal,2012

2. The genetics and pathology of mitochondrial disease;Alston CL;J Pathol,2017

3. Biomarker validation for aging: Lessons from mtDNA heteroplasmy analyses in early cancer detection;Barker PE;Biomark Insights,2009

4. Mitochondrial‐nuclear genome interactions in non‐alcoholic fatty liver disease in mice;Betancourt AM;Biochem J,2014

5. An essential role of the mitochondrial electron transport chain in cell proliferation is to enable aspartate synthesis;Birsoy K;Cell,2015

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