Mitochondrial Cytochrome B gene mutation promotes tumor growth in bladder cancer

Santanu Dasgupta, Mohammad Obaidul Hoque, Sunil Upadhyay, David Sidransky

Research output: Contribution to journalArticlepeer-review

77 Scopus citations


Mitochondria-encoded Cytochrome B (CYTB) gene mutations were reported in different cancers, but the effect of these mutations on cellular metabolism and growth is unknown. In a murine xenograft and human model of bladder cancer, we show the functional effect of overexpression of a 21-bp deletion mutation (mt) of CYTB. Overexpression of mtCYTB generated increased reactive oxygen species (ROS) accompanied by increased oxygen consumption and lactate production. MtCYTB overexpression induced significant tumor growth in vitro and in vivo by triggering rapid cell cycle progression through up-regulation of the nuclear factor-κB2 signaling pathway. Tumor-generated ROS induced in vitro lysis of normal splenocytes. Thus, we present physiologic and functional evidence for the role of a bonafide mitochondrial gene mutation in cancer.

Original languageEnglish (US)
Pages (from-to)700-706
Number of pages7
JournalCancer Research
Issue number3
StatePublished - Feb 1 2008

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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