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

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 a...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2020-10, Vol.80 (19), p.4185-4198
Hauptverfasser: 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
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container_end_page 4198
container_issue 19
container_start_page 4185
container_title Cancer research (Chicago, Ill.)
container_volume 80
creator 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
description 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.
doi_str_mv 10.1158/0008-5472.CAN-20-1079
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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</creator><creatorcontrib>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</creatorcontrib><description>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. 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Jason</creatorcontrib><creatorcontrib>Miller, Bettina</creatorcontrib><creatorcontrib>Chimed, Tugs-Saikhan</creatorcontrib><creatorcontrib>Le, Phuong N.</creatorcontrib><creatorcontrib>Nieto, Cera</creatorcontrib><creatorcontrib>Chowdhury, Farshad N.</creatorcontrib><creatorcontrib>Tyagi, Anit</creatorcontrib><creatorcontrib>Lyons, Traci R.</creatorcontrib><creatorcontrib>Young, Christian D.</creatorcontrib><creatorcontrib>Zhou, Hongmei</creatorcontrib><creatorcontrib>Somerset, Hilary L.</creatorcontrib><creatorcontrib>Wang, Xiao-Jing</creatorcontrib><creatorcontrib>Jimeno, Antonio</creatorcontrib><title>Cancer Cell CD44 Mediates Macrophage/Monocyte-Driven Regulation of Head and Neck Cancer Stem Cells</title><title>Cancer research (Chicago, Ill.)</title><addtitle>CANCER RES</addtitle><addtitle>Cancer Res</addtitle><description>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.</description><subject>Adaptor Proteins, Signal Transducing - metabolism</subject><subject>Animals</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Feedback, Physiological</subject><subject>Female</subject><subject>Head and Neck Neoplasms - metabolism</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Humans</subject><subject>Hyaluronan Receptors - genetics</subject><subject>Hyaluronan Receptors - immunology</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Hyaluronic Acid - metabolism</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Male</subject><subject>Mice, Inbred NOD</subject><subject>Monocytes - metabolism</subject><subject>Monocytes - pathology</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Oncology</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Science &amp; Technology</subject><subject>SOXB1 Transcription Factors - metabolism</subject><subject>Squamous Cell Carcinoma of Head and Neck - metabolism</subject><subject>Squamous Cell Carcinoma of Head and Neck - pathology</subject><subject>Tumor Microenvironment</subject><subject>Tumor-Associated Macrophages - metabolism</subject><subject>Tumor-Associated Macrophages - pathology</subject><subject>Xenograft Model Antitumor Assays</subject><subject>Zinc Finger E-box-Binding Homeobox 1 - genetics</subject><subject>Zinc Finger E-box-Binding Homeobox 1 - metabolism</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqNkUtv1DAUhS0EokPhJ4C8REJp7djXcTZIVVooUqeVeKwtx7mZBjL2EDut-u_xdIYR7Lry6zvH9jmEvOXshHPQp4wxXYCsypPm7LooWcFZVT8jCw5CF5WU8JwsDswReRXjz7wEzuAlORKl5kqDWpC2sd7hRBscR9qcS0mX2A02YaRL66awubUrPF0GH9xDwuJ8Gu7Q06-4mkebhuBp6Okl2o5a39FrdL_o3vBbwvWja3xNXvR2jPhmPx6TH58uvjeXxdXN5y_N2VXhoKxToVjf96XuUIu66qBqJWDnrOtdWYtagAQLlbOiU1YyQMY5cotMu7KzrG-FOCYfd76buV1nKfo02dFspmFtpwcT7GD-P_HDrVmFO6O5VFqpbPB-bzCF3zPGZNZDdPkL1mOYoymlUKLWAJBR2KE5ohgn7A_XcGa2_Zht9mabvcn9mDLv5n6y7t2_bzyo_haSAb0D7rENfXQD5jQP2LbBSlW1lHnGoRnSYwlNmH3K0g9Pl4o_zZ6tNA</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Gomez, Karina E.</creator><creator>Wu, FangLong</creator><creator>Keysar, Stephen B.</creator><creator>Morton, J. 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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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-60fff28de8397d57b45edcacfc29393545a57ca3d6a405e011e1ae08c2da0fb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adaptor Proteins, Signal Transducing - metabolism</topic><topic>Animals</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Feedback, Physiological</topic><topic>Female</topic><topic>Head and Neck Neoplasms - metabolism</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>Humans</topic><topic>Hyaluronan Receptors - genetics</topic><topic>Hyaluronan Receptors - immunology</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Hyaluronic Acid - metabolism</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Male</topic><topic>Mice, Inbred NOD</topic><topic>Monocytes - metabolism</topic><topic>Monocytes - pathology</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Neoplastic Stem Cells - pathology</topic><topic>Oncology</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Science &amp; Technology</topic><topic>SOXB1 Transcription Factors - metabolism</topic><topic>Squamous Cell Carcinoma of Head and Neck - metabolism</topic><topic>Squamous Cell Carcinoma of Head and Neck - pathology</topic><topic>Tumor Microenvironment</topic><topic>Tumor-Associated Macrophages - metabolism</topic><topic>Tumor-Associated Macrophages - pathology</topic><topic>Xenograft Model Antitumor Assays</topic><topic>Zinc Finger E-box-Binding Homeobox 1 - genetics</topic><topic>Zinc Finger E-box-Binding Homeobox 1 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomez, Karina E.</creatorcontrib><creatorcontrib>Wu, FangLong</creatorcontrib><creatorcontrib>Keysar, Stephen B.</creatorcontrib><creatorcontrib>Morton, J. 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Jason</au><au>Miller, Bettina</au><au>Chimed, Tugs-Saikhan</au><au>Le, Phuong N.</au><au>Nieto, Cera</au><au>Chowdhury, Farshad N.</au><au>Tyagi, Anit</au><au>Lyons, Traci R.</au><au>Young, Christian D.</au><au>Zhou, Hongmei</au><au>Somerset, Hilary L.</au><au>Wang, Xiao-Jing</au><au>Jimeno, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer Cell CD44 Mediates Macrophage/Monocyte-Driven Regulation of Head and Neck Cancer Stem Cells</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><stitle>CANCER RES</stitle><addtitle>Cancer Res</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>80</volume><issue>19</issue><spage>4185</spage><epage>4198</epage><pages>4185-4198</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><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, 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. 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subjects Adaptor Proteins, Signal Transducing - metabolism
Animals
Cell Cycle Proteins - metabolism
Cell Line, Tumor
Feedback, Physiological
Female
Head and Neck Neoplasms - metabolism
Head and Neck Neoplasms - pathology
Humans
Hyaluronan Receptors - genetics
Hyaluronan Receptors - immunology
Hyaluronan Receptors - metabolism
Hyaluronic Acid - metabolism
Life Sciences & Biomedicine
Male
Mice, Inbred NOD
Monocytes - metabolism
Monocytes - pathology
Neoplastic Stem Cells - metabolism
Neoplastic Stem Cells - pathology
Oncology
Phosphatidylinositol 3-Kinases - metabolism
Science & Technology
SOXB1 Transcription Factors - metabolism
Squamous Cell Carcinoma of Head and Neck - metabolism
Squamous Cell Carcinoma of Head and Neck - pathology
Tumor Microenvironment
Tumor-Associated Macrophages - metabolism
Tumor-Associated Macrophages - pathology
Xenograft Model Antitumor Assays
Zinc Finger E-box-Binding Homeobox 1 - genetics
Zinc Finger E-box-Binding Homeobox 1 - metabolism
title Cancer Cell CD44 Mediates Macrophage/Monocyte-Driven Regulation of Head and Neck Cancer Stem Cells
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