Mcl-1 regulates reactive oxygen species via NOX4 during chemotherapy-induced senescence

Oncotarget. 2017 Apr 25;8(17):28154-28168. doi: 10.18632/oncotarget.15962.

Abstract

Mcl-1, a Bcl-2 family member, is highly expressed in a variety of human cancers and is believed to enhance tumorigenic potential and chemotherapy resistance through the inhibition of apoptosis and senescence. We previously reported that Mcl-1's regulation of chemotherapy-induced senescence (CIS) is dependent on its ability to prevent reactive oxygen species (ROS) generation. In this report, we demonstrate that Mcl-1-regulated CIS requires not only ROS, but specifically mitochondrial ROS, and that these events are upstream of activation of the DNA damage response, another necessary step toward senescence. Mcl-1's anti-senescence activity also involves the unique ability to inhibit ROS formation by preventing the upregulation of pro-oxidants. Specifically, we found that NADPH oxidases (NOXs) are regulated by Mcl-1 and that NOX4 expression in particular is a required step for CIS induction that is blocked by Mcl-1. Lastly, we illustrate that by preventing expression of NOX4, Mcl-1 limits its availability in the mitochondria, thereby lowering the production of mitochondrial ROS during CIS. Our studies not only define the essential role of Mcl-1 in chemoresistance, but also for the first time link a key pro-survival Bcl-2 family member with the NOX protein family, both of which have significant ramifications in cancer progression.

Keywords: Mcl-1; NOX4; cancer therapy; reactive oxygen species; senescence.

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Antioxidants / metabolism
  • Cell Line, Tumor
  • Cellular Senescence / drug effects*
  • Cellular Senescence / genetics*
  • DNA Damage
  • Gene Expression Regulation
  • Humans
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Myeloid Cell Leukemia Sequence 1 Protein / chemistry
  • Myeloid Cell Leukemia Sequence 1 Protein / genetics*
  • Myeloid Cell Leukemia Sequence 1 Protein / metabolism*
  • NADPH Oxidase 4 / genetics
  • NADPH Oxidase 4 / metabolism*
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Reactive Oxygen Species / metabolism*

Substances

  • Antineoplastic Agents
  • Antioxidants
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Reactive Oxygen Species
  • NADPH Oxidase 4