TrkA Interacts with and Phosphorylates STAT3 to Enhance Gene Transcription and Promote Breast Cancer Stem Cells in Triple-Negative and HER2-Enriched Breast Cancers

Abstract

JAK2–STAT3 and TrkA signaling pathways have been separately implicated in aggressive breast cancers; however, whether they are co-activated or undergo functional interaction has not been thoroughly investigated. Herein we report, for the first time that STAT3 and TrkA are significantly co-overexpressed and co-activated in triple-negative breast cancer (TNBC) and HER2-enriched breast cancer, as shown by immunohistochemical staining and data mining. Through immunofluorescence staining–confocal microscopy and immunoprecipitation–Western blotting, we found that TrkA and STAT3 co-localize and physically interact in the cytoplasm, and the interaction is dependent on STAT3-Y705 phosphorylation. TrkA–STAT3 interaction leads to STAT3 phosphorylation at Y705 by TrkA in breast cancer cells and cell-free kinase assays, indicating that STAT3 is a novel substrate of TrkA. β-NGF-mediated TrkA activation induces TrkA–STAT3 interaction, STAT3 nuclear transport and transcriptional activity, and the expression of STAT3 target genes, SOX2 and MYC. The co-activation of both pathways promotes breast cancer stem cells. Finally, we found that TNBC and HER2-enriched breast cancer with JAK2–STAT3 and TrkA co-activation are positively associated with poor overall metastasis-free and organ-specific metastasis-free survival. Collectively, our study uncovered that TrkA is a novel activating kinase of STAT3, and their co-activation enhances gene transcription and promotes breast cancer stem cells in TNBC and HER2-enriched breast cancer.

Document Details

Document Type
Pub Defense Publication
Publication Date
May 12, 2021
Source ID
10.3390/cancers13102340

Entities

People

  • Alexandra Thomas
  • Angelina T. Regua
  • Austin Arrigo
  • Calvin J. Wagner
  • Daniel Doheny
  • Dongqin Zhu
  • Grace L Wong
  • Guangxu Jin
  • Hui-Wen Lo
  • Jiayuh Lin
  • Jimmy Ruiz
  • Michael D. Chan
  • Noah R. Aguayo
  • Peiqing Sun
  • Roy E Strowd
  • Sara Abu Jalboush
  • Sara G Manore
  • Yang Yu

Organizations

  • Foundation for the National Institutes of Health
  • National Institutes of Health
  • United States Department of Defense

Tags

Fields of Study

  • Biology

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Immunology and Pathology
  • Oncology

Technology Areas

  • AI & ML
  • Biotechnology
  • Biotechnology - Cancer Biotech