Complex‐I Alteration and Enhanced Mitochondrial Fusion Are Associated With Prostate Cancer Progression. Issue 6 (24th November 2015)
- Record Type:
- Journal Article
- Title:
- Complex‐I Alteration and Enhanced Mitochondrial Fusion Are Associated With Prostate Cancer Progression. Issue 6 (24th November 2015)
- Main Title:
- Complex‐I Alteration and Enhanced Mitochondrial Fusion Are Associated With Prostate Cancer Progression
- Authors:
- Philley, Julie V.
Kannan, Anbarasu
Qin, Wenyi
Sauter, Edward R.
Ikebe, Mitsuo
Hertweck, Kate L.
Troyer, Dean A.
Semmes, Oliver J.
Dasgupta, Santanu - Abstract:
- Abstract : Mitochondria (mt) encoded respiratory complex‐I (RCI) mutations and their pathogenicity remain largely unknown in prostate cancer (PCa). Little is known about the role of mtDNA loss on mt integrity in PCa. We determined mtDNA mutation in human and mice PCa and assessed the impact of mtDNA depletion on mt integrity. We also examined whether the circulating exosomes from PCa patients are transported to mt and carry mtDNA or mt proteins. We have employed next generation sequencing of the whole mt genome in human and Hi‐myc PCa. The impact of mtDNA depletion on mt integrity, presence of mtDNA, and protein in sera exosomes was determined. A co‐culture of human PCa cells and the circulating exosomes followed by confocal imaging determined co‐localization of exosomes and mt. We observed frequent RCI mutations in human and Hi‐myc PCa which disrupted corresponding complex protein expression. Depletion of mtDNA in PCa cells influenced mt integrity, increased expression of MFN1, MFN2, PINK1, and decreased expression of MT‐TFA. Increased mt fusion and expression of PINK1 and DNM1L were also evident in the Hi‐myc tumors. RCI‐mtDNA, MFN2, and IMMT proteins were detected in the circulating exosomes of men with benign prostate hyperplasia (BPH) and progressive PCa. Circulating exosomes and mt co‐localized in PCa cells. Our study identified new pathogenic RCI mutations in PCa and defined the impact of mtDNA loss on mt integrity. Presence of mtDNA and mt proteins in the circulatingAbstract : Mitochondria (mt) encoded respiratory complex‐I (RCI) mutations and their pathogenicity remain largely unknown in prostate cancer (PCa). Little is known about the role of mtDNA loss on mt integrity in PCa. We determined mtDNA mutation in human and mice PCa and assessed the impact of mtDNA depletion on mt integrity. We also examined whether the circulating exosomes from PCa patients are transported to mt and carry mtDNA or mt proteins. We have employed next generation sequencing of the whole mt genome in human and Hi‐myc PCa. The impact of mtDNA depletion on mt integrity, presence of mtDNA, and protein in sera exosomes was determined. A co‐culture of human PCa cells and the circulating exosomes followed by confocal imaging determined co‐localization of exosomes and mt. We observed frequent RCI mutations in human and Hi‐myc PCa which disrupted corresponding complex protein expression. Depletion of mtDNA in PCa cells influenced mt integrity, increased expression of MFN1, MFN2, PINK1, and decreased expression of MT‐TFA. Increased mt fusion and expression of PINK1 and DNM1L were also evident in the Hi‐myc tumors. RCI‐mtDNA, MFN2, and IMMT proteins were detected in the circulating exosomes of men with benign prostate hyperplasia (BPH) and progressive PCa. Circulating exosomes and mt co‐localized in PCa cells. Our study identified new pathogenic RCI mutations in PCa and defined the impact of mtDNA loss on mt integrity. Presence of mtDNA and mt proteins in the circulating exosomes implicated their usefulness for biomarker development. J. Cell. Physiol. 231: 1364–1374, 2016. © 2015 Wiley Periodicals, Inc. … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 231:Issue 6(2016:Jun.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 231:Issue 6(2016:Jun.)
- Issue Display:
- Volume 231, Issue 6 (2016)
- Year:
- 2016
- Volume:
- 231
- Issue:
- 6
- Issue Sort Value:
- 2016-0231-0006-0000
- Page Start:
- 1364
- Page End:
- 1374
- Publication Date:
- 2015-11-24
- Subjects:
- Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.25240 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
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