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Cancer Cell CD44 Mediates Macrophage/Monocyte-Driven Regulation of Head and Neck Cancer Stem Cells.
Gomez, Karina E; Wu, FangLong; Keysar, Stephen B; Morton, J Jason; Miller, Bettina; Chimed, Tugs-Saikhan; Le, Phuong N; Nieto, Cera; Chowdhury, Farshad N; Tyagi, Anit; Lyons, Traci R; Young, Christian D; Zhou, Hongmei; Somerset, Hilary L; Wang, Xiao-Jing; Jimeno, Antonio.
Affiliation
  • Gomez KE; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Wu F; Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Keysar SB; State Key Laboratory of Oral Diseases, Department of Oral Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Morton JJ; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Miller B; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Chimed TS; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Le PN; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Nieto C; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Chowdhury FN; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Tyagi A; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Lyons TR; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Young CD; Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Zhou H; Gates Center for Regenerative Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Somerset HL; Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Wang XJ; State Key Laboratory of Oral Diseases, Department of Oral Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Jimeno A; Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Cancer Res ; 80(19): 4185-4198, 2020 10 01.
Article in En | MEDLINE | ID: mdl-32816856
ABSTRACT
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, respectively. 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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neoplastic Stem Cells / Hyaluronan Receptors / Squamous Cell Carcinoma of Head and Neck / Tumor-Associated Macrophages / Head and Neck Neoplasms Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Cancer Res Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neoplastic Stem Cells / Hyaluronan Receptors / Squamous Cell Carcinoma of Head and Neck / Tumor-Associated Macrophages / Head and Neck Neoplasms Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Cancer Res Year: 2020 Document type: Article
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