4.8 Article

Cancer Cell CD44 Mediates Macrophage/Monocyte-Driven Regulation of Head and Neck Cancer Stem Cells

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CANCER RESEARCH
卷 80, 期 19, 页码 4185-4198

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-20-1079

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资金

  1. NIH [R01CA149456, R21DE019712, R01DE024371, R01CA21169601A1, ACS RSG16171010CSM]
  2. Charles C. Gates Center for Stem Cell Biology
  3. Daniel and Janet Mordecai Foundation
  4. VA Merit Award [I01BX003232]
  5. University of Colorado Skin Diseases Research Center support grant [P30-AR057212]
  6. Ruth L. Kirschstein National Research Service award [T32CA17468]
  7. CCTSI TL1 Pre-doctoral fellowship [TR002533]
  8. Training in Otolaryngology [T32DC012280]
  9. University of Colorado Cancer Center support grant [P30-CA046934]
  10. [DE020649]

向作者/读者索取更多资源

Tumor-associated macrophages (TAM) in the tumor microenvironment (TME) cooperate with cancer stem cells (CSC) to maintain stemness. We recently identified cluster of differentiation 44 (CD44) as a surface marker defining head and neck squamous cell carcinoma (HNSCC) CSC. PI3K-4EBP1-SOX2 activation and signaling regulate CSC properties, yet the upstream molecular control of this pathway and the mechanisms underlying cross-talk between TAM and CSC in HNSCC remain largely unknown. Because CD44 is a molecular mediator in the TME, we propose here that TAM-influenced CD44 signaling could mediate stemness via the PI3K-4EBP1-SOX2 pathway, possibly by modulating availability of hyaluronic acid (HA), the main CD44 ligand. HNSCC IHC was used to identify TAM/CSC relationships, and in vitro coculture spheroid models and in vivo mouse models were used to identify the influence of TAMs on CSC function via CD44. Patient HNSCC-derived TAMs were positively and negatively associated with CSC marker expression at noninvasive and invasive edge regions, respec-tively. TAMs increased availability of HA and increased cancer cell invasion. HA binding to CD44 increased PI3K-4EBP1-SOX2 signaling and the CSC fraction, whereas CD44-VCAM-1 binding promoted invasive signaling by ezrin/PI3K. In vivo, targeting CD44 decreased PI3K-4EBP1-SOX2 signaling, tumor growth, and CSC. TAM depletion in syngeneic and humanized mouse models also diminished growth and CSC numbers. Finally, a CD44 isoform switch regulated epithelial-to-mesenchymal plasticity as standard form of CD44 and CD44v8-10 determined invasive and tumorigenic phenotypes, respectively. We have established a mechanistic link between TAMs and CSCs in HNSCC that is mediated by CD44 intracellular signaling in response to extracellular signals. Significance: These findings establish a mechanistic link between tumor cell CD44, TAM, and CSC properties at the tumor-stroma interface that can serve as a vital area of focus for target and drug discovery.

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