Mitochondrial respiratory complex I dysfunction promotes tumorigenesis through ROS alteration and AKT activation

LK Sharma, H Fang, J Liu, R Vartak… - Human molecular …, 2011 - academic.oup.com
LK Sharma, H Fang, J Liu, R Vartak, J Deng, Y Bai
Human molecular genetics, 2011academic.oup.com
Previously, we have shown that a heteroplasmic mutation in mitochondrial DNA-encoded
complex I ND5 subunit gene resulted in an enhanced tumorigenesis through increased
resistance to apoptosis. Here we report that the tumorigenic phenotype associated with
complex I dysfunction could be reversed by introducing a yeast NADH quinone
oxidoreductase (NDI1) gene. The NDI1 mediated electron transfer from NADH to Co-Q,
bypassed the defective complex I and restored oxidative phosphorylation in the host cells …
Abstract
Previously, we have shown that a heteroplasmic mutation in mitochondrial DNA-encoded complex I ND5 subunit gene resulted in an enhanced tumorigenesis through increased resistance to apoptosis. Here we report that the tumorigenic phenotype associated with complex I dysfunction could be reversed by introducing a yeast NADH quinone oxidoreductase (NDI1) gene. The NDI1 mediated electron transfer from NADH to Co-Q, bypassed the defective complex I and restored oxidative phosphorylation in the host cells. Alternatively, suppression of complex I activity by a specific inhibitor, rotenone or induction of oxidative stress by paraquat led to an increase in the phosphorylation of v-AKT murine thymoma viral oncogene (AKT) and enhanced the tumorigenesis. On the other hand, antioxidant treatment can ameliorate the reactive oxygen species-mediated AKT activation and reverse the tumorigenicity of complex I-deficient cells. Our results suggest that complex I defects could promote tumorigenesis through induction of oxidative stress and activation of AKT pathway.
Oxford University Press