Nature Communications (Mar 2022)

S100A9-CXCL12 activation in BRCA1-mutant breast cancer promotes an immunosuppressive microenvironment associated with resistance to immunotherapy

  • Jianjie Li,
  • Xiaodong Shu,
  • Jun Xu,
  • Sek Man Su,
  • Un In Chan,
  • Lihua Mo,
  • Jianlin Liu,
  • Xin Zhang,
  • Ragini Adhav,
  • Qiang Chen,
  • Yuqing Wang,
  • Tingting An,
  • Xu Zhang,
  • Xueying Lyu,
  • Xiaoling Li,
  • Josh Haipeng Lei,
  • Kai Miao,
  • Heng Sun,
  • Fuqiang Xing,
  • Aiping Zhang,
  • Chuxia Deng,
  • Xiaoling Xu

DOI
https://doi.org/10.1038/s41467-022-29151-5
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 19

Abstract

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Defects in BRCA1, a gene involved in homologous recombination DNA repair, are common in triple negative breast cancer. Here the authors show that Brca1 deficiency in preclinical breast cancer models is associated with the accumulation of myeloid derived suppressive cells and resistance to immune checkpoint blockade, that could be overcome by targeting S100A9 and CXCL12.