Nature Communications (Feb 2024)

The IL6/JAK/STAT3 signaling axis is a therapeutic vulnerability in SMARCB1-deficient bladder cancer

  • Chandra Sekhar Amara,
  • Karthik Reddy Kami Reddy,
  • Yang Yuntao,
  • Yuen San Chan,
  • Danthasinghe Waduge Badrajee Piyarathna,
  • Lacey Elizabeth Dobrolecki,
  • David J. H. Shih,
  • Zhongcheng Shi,
  • Jun Xu,
  • Shixia Huang,
  • Matthew J. Ellis,
  • Andrea B. Apolo,
  • Leomar Y. Ballester,
  • Jianjun Gao,
  • Donna E. Hansel,
  • Yair Lotan,
  • H. Courtney Hodges,
  • Seth P. Lerner,
  • Chad J. Creighton,
  • Arun Sreekumar,
  • W. Jim Zheng,
  • Pavlos Msaouel,
  • Shyam M. Kavuri,
  • Nagireddy Putluri

DOI
https://doi.org/10.1038/s41467-024-45132-2
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 16

Abstract

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Abstract SMARCB1 loss has long been observed in many solid tumors. However, there is a need to elucidate targetable pathways driving growth and metastasis in SMARCB1-deficient tumors. Here, we demonstrate that SMARCB1 deficiency, defined as genomic SMARCB1 copy number loss associated with reduced mRNA, drives disease progression in patients with bladder cancer by engaging STAT3. SMARCB1 loss increases the chromatin accessibility of the STAT3 locus in vitro. Orthotopically implanted SMARCB1 knockout (KO) cell lines exhibit increased tumor growth and metastasis. SMARCB1-deficient tumors show an increased IL6/JAK/STAT3 signaling axis in in vivo models and patients. Furthermore, a pSTAT3 selective inhibitor, TTI-101, reduces tumor growth in SMARCB1 KO orthotopic cell line-derived xenografts and a SMARCB1-deficient patient derived xenograft model. We have identified a gene signature generated from SMARCB1 KO tumors that predicts SMARCB1 deficiency in patients. Overall, these findings support the clinical evaluation of STAT3 inhibitors for the treatment of SMARCB1-deficient bladder cancer.