2014
DOI: 10.1007/s11515-014-1332-0
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Functional implications of mitochondrial reactive oxygen species generated by oncogenic viruses

Abstract: Between 15–20% of human cancers are associated with infection by oncogenic viruses. Oncogenic viruses, including HPV, HBV, HCV and HTLV-1, target mitochondria to influence cell proliferation and survival. Oncogenic viral gene products also trigger the production of reactive oxygen species which can elicit oxidative DNA damage and potentiate oncogenic host signaling pathways. Viral oncogenes may also subvert mitochondria quality control mechanisms such as mitophagy and metabolic adaptation pathways to promote v… Show more

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Cited by 11 publications
(9 citation statements)
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“…We examined the cellular energy metabolism with a focus on mitochondria and glycolysis. Virus infection is known to impair mitochondrial function in host cells [25,38,39]. In our study, the OCR and expression of UCP1 in IAV cells were lower than those in the control cells (Fig.…”
Section: Discussionmentioning
confidence: 51%
See 1 more Smart Citation
“…We examined the cellular energy metabolism with a focus on mitochondria and glycolysis. Virus infection is known to impair mitochondrial function in host cells [25,38,39]. In our study, the OCR and expression of UCP1 in IAV cells were lower than those in the control cells (Fig.…”
Section: Discussionmentioning
confidence: 51%
“…Therefore, mitochondria and glycolysis play important roles in cellular energy metabolism. Recent studies have revealed that mitochondria are responsible for regulating the mammalian innate immune response [20,21], particularly with regard to infection with RNA viruses (including influenza virus) [22,23,24,25,26,27]. Further, the effect of viruses on glycolytic metabolism has also been reported [28,29,30,31,32,33].…”
Section: Introductionmentioning
confidence: 99%
“…High-risk HPV infection may cause a series of mitochondrial dysfunction by accelerating the production of ROS [35,36]. Warowicka et al observed that both mtCN and ROS were increased during cervical cancer development [28].…”
Section: Discussionmentioning
confidence: 99%
“…High-risk HPV infection may cause a series of mitochondrial dysfunction by accelerating the production of ROS [34,35]. Warowicka et al observed that both mtCN and ROS were increased during cervical cancer development [29].…”
Section: Discussionmentioning
confidence: 99%