Research Paper Volume 4, Issue 12 pp 932—951

IL1- and TGFβ-Nox4 signaling, oxidative stress and DNA damage response are shared features of replicative, oncogene-induced, and drug-induced paracrine ‘Bystander senescence’

Sona Hubackova1, , Katerina Krejcikova1, , Jiri Bartek1,2, , Zdenek Hodny1, ,

  • 1 Department of Genome Integrity, Institute of Molecular Genetics, v.v.i., Academy of Sciences of the Czech Republic, Prague, Czech Republic
  • 2 Danish Cancer Society Research Center, Copenhagen, Denmark

Received: December 4, 2012       Accepted: December 19, 2012       Published: December 30, 2012      

https://doi.org/10.18632/aging.100520
How to Cite

Abstract

Many cancers arise at sites of infection and inflammation. Cellular senescence, a permanent state of cell cycle arrest that provides a barrier against tumorigenesis, is accompanied by elevated proinflammatory cytokines such as IL1, IL6, IL8 and TNFα. Here we demonstrate that media conditioned by cells undergoing any of the three main forms of senescence, i.e. replicative, oncogene- and drug-induced, contain high levels of IL1, IL6, and TGFb capable of inducing reactive oxygen species (ROS)-mediated DNA damage response (DDR). Persistent cytokine signaling and activated DDR evoke senescence in normal bystander cells, accompanied by activation of the JAK/STAT, TGFβ/SMAD and IL1/NFκB signaling pathways. Whereas inhibition of IL6/STAT signaling had no effect on DDR induction in bystander cells, inhibition of either TGFβ/SMAD or IL1/NFκB pathway resulted in decreased ROS production and reduced DDR in bystander cells. Simultaneous inhibition of both TGFβ/SMAD and IL1/NFκB pathways completely suppressed DDR indicating that IL1 and TGFβ cooperate to induce and/or maintain bystander senescence. Furthermore, the observed IL1- and TGFβ-induced expression of NAPDH oxidase Nox4 indicates a mechanistic link between the senescence-associated secretory phenotype (SASP) and DNA damage signaling as a feature shared by development of all major forms of paracrine bystander senescence.

Abbreviations

bDIS: “bystander” drug-induced senescence; bOIS: “bystander” oncogene-induced senescence; bRS: “bystander” replicative senescence; DAPI: 4’,6-diamidino-2-phenylindole; DDR: DNA damage response; GAPDH: glyceraldehyde 3-phosphate dehydrogenase; DCF: 2’,7’-dichlorofluorescein; IFN: interferon; IKK: IκB kinase; IL: interleukin; JAK: Janus kinase/just another kinase; NFκB: nuclear factor kappa B; pDIS: “parental” drug-induced senescence; pOIS: “parental” oncogene-induced senescence; pRS: “parental” replicative senescence; PML: promyelocytic leukemia protein; PML NBs: promyelocytic leukemia nuclear bodies; ROS: reactive oxygen species; SA-β-gal: senescence-associated beta-galactosidase;; SAS: senescence-associated secretome; STAT: signal transducers and activators of transcription; TGFβ: transforming growth factor beta; TNFα: tumor necrosis factor alpha; TMRE: tetramethylrhodamine ethyl ester.