Stat3 orchestrates interaction between endothelial and tumor cells and inhibition of Stat3 suppresses brain metastasis of breast cancer cells

Hsueh Te Lee, Jianfei Xue, Ping Chieh Chou, Aidong Zhou, Phillip Yang, Charles A. Conrad, Kenneth D. Aldape, Waldemar Priebe, Cam Patterson, Raymond Sawaya, Keping Xie, Suyun Huang

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

Brain metastasis is a major cause of morbidity and mortality in patients with breast cancer. Our previous studies indicated that Stat3 plays an important role in brain metastasis. Here, we present evidence that Stat3 functions at the level of the microenvironment of brain metastases. Stat3 controlled constitutive and inducible VEGFR2 expression in tumor-associated brain endothelial cells. Furthermore, inhibition of Stat3 by WP1066 decreased the incidence of brain metastases and increased survival in a preclinical model of breast cancer brain metastasis. WP1066 inhibited Stat3 activation in tumor-associated endothelial cells, reducing their infiltration and angiogenesis. WP1066 also inhibited breast cancer cell invasion. Our results indicate that WP1066 can inhibit tumor angiogenesis and brain metastasis mediated by Stat3 in endothelial and tumor cells.

Original languageEnglish (US)
Pages (from-to)10016-10029
Number of pages14
JournalOncotarget
Volume6
Issue number12
DOIs
StatePublished - 2015

Keywords

  • Brain endothelial cells
  • Brain metastasis
  • Stat3
  • Stat3 inhibitor
  • VEGFR2

ASJC Scopus subject areas

  • Oncology

MD Anderson CCSG core facilities

  • Research Animal Support Facility
  • Tissue Biospecimen and Pathology Resource

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