Specific N-cadherin-dependent pathways drive human breast cancer dormancy in bone marrow

Life Sci Alliance. 2021 Jun 2;4(7):e202000969. doi: 10.26508/lsa.202000969. Print 2021 Jul.

Abstract

The challenge for treating breast cancer (BC) is partly due to long-term dormancy driven by cancer stem cells (CSCs) capable of evading immune response and resist chemotherapy. BC cells show preference for the BM, resulting in poor prognosis. CSCs use connexin 43 (Cx43) to form gap junctional intercellular communication with BM niche cells, fibroblasts, and mesenchymal stem cells (MSCs). However, Cx43 is an unlikely target to reverse BC dormancy because of its role as a hematopoietic regulator. We found N-cadherin (CDH2) and its associated pathways as potential drug targets. CDH2, highly expressed in CSCs, interacts intracellularly with Cx43, colocalizes with Cx43 in BC cells within BM biopsies of patients, and is required for Cx43-mediated gap junctional intercellular communication with BM niche cells. Notably, CDH2 and anti-apoptotic pathways maintained BC dormancy. We thereby propose these pathways as potential pharmacological targets to prevent dormancy and chemosensitize resistant CSCs.

Publication types

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

MeSH terms

  • Antigens, CD / genetics
  • Antigens, CD / metabolism*
  • Bone Marrow / metabolism
  • Breast Neoplasms / metabolism*
  • Cadherins / genetics
  • Cadherins / metabolism*
  • Cadherins / physiology
  • Connexin 43 / genetics
  • Connexin 43 / metabolism*
  • Drug Resistance, Neoplasm / physiology
  • Female
  • Gap Junctions / metabolism
  • Gap Junctions / pathology
  • Humans
  • Mesenchymal Stem Cells / metabolism
  • Neoplasm Metastasis / pathology
  • Neoplastic Stem Cells / metabolism
  • Tumor Escape / physiology

Substances

  • Antigens, CD
  • CDH2 protein, human
  • Cadherins
  • Connexin 43
  • GJA1 protein, human

Associated data

  • PDB/3Q2W
  • PDB/2LL2