A Transient Pseudosenescent Secretome Promotes Tumor Growth after Antiangiogenic Therapy Withdrawal

Cell Rep. 2018 Dec 26;25(13):3706-3720.e8. doi: 10.1016/j.celrep.2018.12.017.

Abstract

VEGF receptor tyrosine kinase inhibitors (VEGFR TKIs) approved to treat multiple cancer types can promote metastatic disease in certain limited preclinical settings. Here, we show that stopping VEGFR TKI treatment after resistance can lead to rebound tumor growth that is driven by cellular changes resembling senescence-associated secretory phenotypes (SASPs) known to promote cancer progression. A SASP-mimicking antiangiogenic therapy-induced secretome (ATIS) was found to persist during short withdrawal periods, and blockade of known SASP regulators, including mTOR and IL-6, could blunt rebound effects. Critically, senescence hallmarks ultimately reversed after long drug withdrawal periods, suggesting that the transition to a permanent growth-arrested senescent state was incomplete and the hijacking of SASP machinery ultimately transient. These findings may account for the highly diverse and reversible cytokine changes observed in VEGF inhibitor-treated patients, and suggest senescence-targeted therapies ("senotherapeutics")-particularly those that block SASP regulation-may improve outcomes in patients after VEGFR TKI failure.

Keywords: IL-6; SASP; VEGF RTKI; antiangiogenic therapy; mTOR; metastasis; rebound; resistance; secretome; senescence.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Angiogenesis Inhibitors / therapeutic use*
  • Animals
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cellular Senescence* / drug effects
  • Drug Resistance, Neoplasm / drug effects
  • Humans
  • Interleukin-6 / metabolism
  • Mice, Inbred BALB C
  • Neoplasm Metastasis
  • Neoplasms / blood supply
  • Neoplasms / drug therapy*
  • Neoplasms / pathology*
  • Phenotype
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Proteome / metabolism*
  • Receptors, Vascular Endothelial Growth Factor / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Angiogenesis Inhibitors
  • Interleukin-6
  • Protein Kinase Inhibitors
  • Proteome
  • Receptors, Vascular Endothelial Growth Factor
  • TOR Serine-Threonine Kinases