Activation of Matrix Hyaluronan-Mediated CD44 Signaling, Epigenetic Regulation and Chemoresistance in Head and Neck Cancer Stem Cells
Head and neck squamous cell carcinoma (HNSCC) is a solid tumor composed by a genotypically and phenotypically heterogeneous population of neoplastic cells types. High recurrence rate and regional metastases lead to major morbidity and mortality. Recently, many studies have focused on cellular and mo...
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description | Head and neck squamous cell carcinoma (HNSCC) is a solid tumor composed by a genotypically and phenotypically heterogeneous population of neoplastic cells types. High recurrence rate and regional metastases lead to major morbidity and mortality. Recently, many studies have focused on cellular and molecular mechanisms of tumor progression that can help to predict prognosis and to choose the best therapeutic approach for HNSCC patients. Hyaluronan (HA), an important glycosaminoglycan component of the extracellular matrix (ECM), and its major cell surface receptor, CD44, have been suggested to be important cellular mediators influencing tumor progression and treatment resistance in head and neck cancer. HNSCC contains a small subpopulation of cells that exhibit a hallmark of CD44-expressing cancer stem cell (CSC) properties with self-renewal, multipotency, and a unique potential for tumor initiation. HA has been shown to stimulate a variety of CSC functions including self-renewal, clone formation and differentiation. This review article will present current evidence for the existence of a unique small population of CD44v3
ALDH
-expressing CSCs in HNSCC. A special focus will be placed on the role of HA/CD44-induced oncogenic signaling and histone methyltransferase, DOT1L activities in regulating histone modifications (via epigenetic changes) and miRNA activation. Many of these events are essential for the CSC properties such as Nanog/Oct4/Sox2 expression, spheroid/clone formation, self-renewal, tumor cell migration/invasion, survival and chemotherapeutic drug resistance in HA-activated head and neck cancer. These newly-discovered HA/CD44-mediated oncogenic signaling pathways delineate unique tumor dynamics with implications for defining the drivers of HNSCC progression processes. Most importantly, the important knowledge obtained from HA/CD44-regulated CSC signaling and functional activation could provide new information regarding the design of novel drug targets to overcome current therapeutic drug resistance which will have significant treatment implications for head and neck cancer patients. |
doi_str_mv | 10.3390/ijms18091849 |
format | Article |
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ALDH
-expressing CSCs in HNSCC. A special focus will be placed on the role of HA/CD44-induced oncogenic signaling and histone methyltransferase, DOT1L activities in regulating histone modifications (via epigenetic changes) and miRNA activation. Many of these events are essential for the CSC properties such as Nanog/Oct4/Sox2 expression, spheroid/clone formation, self-renewal, tumor cell migration/invasion, survival and chemotherapeutic drug resistance in HA-activated head and neck cancer. These newly-discovered HA/CD44-mediated oncogenic signaling pathways delineate unique tumor dynamics with implications for defining the drivers of HNSCC progression processes. Most importantly, the important knowledge obtained from HA/CD44-regulated CSC signaling and functional activation could provide new information regarding the design of novel drug targets to overcome current therapeutic drug resistance which will have significant treatment implications for head and neck cancer patients.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms18091849</identifier><identifier>PMID: 28837080</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Activation ; Animals ; Biomarkers ; CD44 antigen ; Cell self-renewal ; Cell surface ; Chemoresistance ; Cloning ; Disease Progression ; Drug development ; Drug resistance ; Drug Resistance, Neoplasm - genetics ; Epigenesis, Genetic ; Epigenetics ; Extracellular Matrix ; Gene Expression Regulation, Neoplastic ; Head & neck cancer ; Head and Neck Neoplasms - genetics ; Head and Neck Neoplasms - metabolism ; Head and Neck Neoplasms - pathology ; Histone methyltransferase ; Histone-Lysine N-Methyltransferase - genetics ; Histone-Lysine N-Methyltransferase - metabolism ; Humans ; Hyaluronan Receptors - metabolism ; Hyaluronic acid ; Hyaluronic Acid - chemistry ; Hyaluronic Acid - metabolism ; Isoenzymes - metabolism ; Medical prognosis ; Metastases ; Methyltransferases - genetics ; Methyltransferases - metabolism ; MicroRNAs - genetics ; miRNA ; Molecular modelling ; Morbidity ; Neoplastic Stem Cells - drug effects ; Neoplastic Stem Cells - metabolism ; Oct-4 protein ; Patients ; Protein Binding ; Retinal Dehydrogenase - metabolism ; Review ; Signal Transduction ; Squamous cell carcinoma ; Stem cells ; Treatment resistance</subject><ispartof>International journal of molecular sciences, 2017-08, Vol.18 (9), p.1849</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-ef8187fb3b5fa4956f6fea190708c0fb33ef7421af37d069accd21550d1c576b3</citedby><cites>FETCH-LOGICAL-c478t-ef8187fb3b5fa4956f6fea190708c0fb33ef7421af37d069accd21550d1c576b3</cites><orcidid>0000-0003-3172-9251</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618498/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618498/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28837080$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bourguignon, Lilly Y W</creatorcontrib><creatorcontrib>Earle, Christine</creatorcontrib><creatorcontrib>Shiina, Marisa</creatorcontrib><title>Activation of Matrix Hyaluronan-Mediated CD44 Signaling, Epigenetic Regulation and Chemoresistance in Head and Neck Cancer Stem Cells</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Head and neck squamous cell carcinoma (HNSCC) is a solid tumor composed by a genotypically and phenotypically heterogeneous population of neoplastic cells types. High recurrence rate and regional metastases lead to major morbidity and mortality. Recently, many studies have focused on cellular and molecular mechanisms of tumor progression that can help to predict prognosis and to choose the best therapeutic approach for HNSCC patients. Hyaluronan (HA), an important glycosaminoglycan component of the extracellular matrix (ECM), and its major cell surface receptor, CD44, have been suggested to be important cellular mediators influencing tumor progression and treatment resistance in head and neck cancer. HNSCC contains a small subpopulation of cells that exhibit a hallmark of CD44-expressing cancer stem cell (CSC) properties with self-renewal, multipotency, and a unique potential for tumor initiation. HA has been shown to stimulate a variety of CSC functions including self-renewal, clone formation and differentiation. This review article will present current evidence for the existence of a unique small population of CD44v3
ALDH
-expressing CSCs in HNSCC. A special focus will be placed on the role of HA/CD44-induced oncogenic signaling and histone methyltransferase, DOT1L activities in regulating histone modifications (via epigenetic changes) and miRNA activation. Many of these events are essential for the CSC properties such as Nanog/Oct4/Sox2 expression, spheroid/clone formation, self-renewal, tumor cell migration/invasion, survival and chemotherapeutic drug resistance in HA-activated head and neck cancer. These newly-discovered HA/CD44-mediated oncogenic signaling pathways delineate unique tumor dynamics with implications for defining the drivers of HNSCC progression processes. Most importantly, the important knowledge obtained from HA/CD44-regulated CSC signaling and functional activation could provide new information regarding the design of novel drug targets to overcome current therapeutic drug resistance which will have significant treatment implications for head and neck cancer patients.</description><subject>Activation</subject><subject>Animals</subject><subject>Biomarkers</subject><subject>CD44 antigen</subject><subject>Cell self-renewal</subject><subject>Cell surface</subject><subject>Chemoresistance</subject><subject>Cloning</subject><subject>Disease Progression</subject><subject>Drug development</subject><subject>Drug resistance</subject><subject>Drug Resistance, Neoplasm - genetics</subject><subject>Epigenesis, Genetic</subject><subject>Epigenetics</subject><subject>Extracellular Matrix</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Head & neck cancer</subject><subject>Head and Neck Neoplasms - genetics</subject><subject>Head and Neck Neoplasms - metabolism</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Histone methyltransferase</subject><subject>Histone-Lysine N-Methyltransferase - genetics</subject><subject>Histone-Lysine N-Methyltransferase - metabolism</subject><subject>Humans</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Hyaluronic acid</subject><subject>Hyaluronic Acid - chemistry</subject><subject>Hyaluronic Acid - metabolism</subject><subject>Isoenzymes - metabolism</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Methyltransferases - genetics</subject><subject>Methyltransferases - metabolism</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>Molecular modelling</subject><subject>Morbidity</subject><subject>Neoplastic Stem Cells - drug effects</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Oct-4 protein</subject><subject>Patients</subject><subject>Protein Binding</subject><subject>Retinal Dehydrogenase - metabolism</subject><subject>Review</subject><subject>Signal Transduction</subject><subject>Squamous cell carcinoma</subject><subject>Stem cells</subject><subject>Treatment resistance</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU9v1DAQxSNERUvhxhlZ4sKhAf9N4gtSlRYWqQWJwtnyOuPUS2IvtlO1H4DvTcK21cJpRjM_Pc2bVxSvCH7HmMTv3WZMpMGSNFw-KY4Ip7TEuKqf7vWHxfOUNhhTRoV8VhzSpmE1bvBR8fvUZHejswseBYsudY7uFq3u9DDF4LUvL6FzOkOH2jPO0ZXrvR6c70_Q-db14CE7g75BPw07De1n8hrGECG5lLU3gJxHK9Dd390XMD9Ru4wjusowohaGIb0oDqweEry8r8fFj4_n39tVefH10-f29KI0vG5yCbYhTW3XbC2s5lJUtrKgicSzF4PnOQNbc0q0ZXWHK6mN6SgRAnfEiLpas-Piw053O61H6Az4HPWgttGNOt6poJ36d-PdterDjRLV8t5mFnh7LxDDrwlSVqNLZragPYQpKSIZJZWsOJ_RN_-hmzDF-XsLJSglvBaL4MmOMjGkFME-HkOwWvJV-_nO-Ot9A4_wQ6DsD_h2oos</recordid><startdate>20170824</startdate><enddate>20170824</enddate><creator>Bourguignon, Lilly Y W</creator><creator>Earle, Christine</creator><creator>Shiina, Marisa</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3172-9251</orcidid></search><sort><creationdate>20170824</creationdate><title>Activation of Matrix Hyaluronan-Mediated CD44 Signaling, Epigenetic Regulation and Chemoresistance in Head and Neck Cancer Stem Cells</title><author>Bourguignon, Lilly Y W ; Earle, Christine ; Shiina, Marisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-ef8187fb3b5fa4956f6fea190708c0fb33ef7421af37d069accd21550d1c576b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Activation</topic><topic>Animals</topic><topic>Biomarkers</topic><topic>CD44 antigen</topic><topic>Cell self-renewal</topic><topic>Cell surface</topic><topic>Chemoresistance</topic><topic>Cloning</topic><topic>Disease Progression</topic><topic>Drug development</topic><topic>Drug resistance</topic><topic>Drug Resistance, Neoplasm - genetics</topic><topic>Epigenesis, Genetic</topic><topic>Epigenetics</topic><topic>Extracellular Matrix</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Head & neck cancer</topic><topic>Head and Neck Neoplasms - genetics</topic><topic>Head and Neck Neoplasms - metabolism</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>Histone methyltransferase</topic><topic>Histone-Lysine N-Methyltransferase - genetics</topic><topic>Histone-Lysine N-Methyltransferase - metabolism</topic><topic>Humans</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Hyaluronic acid</topic><topic>Hyaluronic Acid - chemistry</topic><topic>Hyaluronic Acid - metabolism</topic><topic>Isoenzymes - metabolism</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Methyltransferases - genetics</topic><topic>Methyltransferases - metabolism</topic><topic>MicroRNAs - genetics</topic><topic>miRNA</topic><topic>Molecular modelling</topic><topic>Morbidity</topic><topic>Neoplastic Stem Cells - drug effects</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Oct-4 protein</topic><topic>Patients</topic><topic>Protein Binding</topic><topic>Retinal Dehydrogenase - metabolism</topic><topic>Review</topic><topic>Signal Transduction</topic><topic>Squamous cell carcinoma</topic><topic>Stem cells</topic><topic>Treatment resistance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bourguignon, Lilly Y W</creatorcontrib><creatorcontrib>Earle, Christine</creatorcontrib><creatorcontrib>Shiina, Marisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bourguignon, Lilly Y W</au><au>Earle, Christine</au><au>Shiina, Marisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activation of Matrix Hyaluronan-Mediated CD44 Signaling, Epigenetic Regulation and Chemoresistance in Head and Neck Cancer Stem Cells</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2017-08-24</date><risdate>2017</risdate><volume>18</volume><issue>9</issue><spage>1849</spage><pages>1849-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Head and neck squamous cell carcinoma (HNSCC) is a solid tumor composed by a genotypically and phenotypically heterogeneous population of neoplastic cells types. High recurrence rate and regional metastases lead to major morbidity and mortality. Recently, many studies have focused on cellular and molecular mechanisms of tumor progression that can help to predict prognosis and to choose the best therapeutic approach for HNSCC patients. Hyaluronan (HA), an important glycosaminoglycan component of the extracellular matrix (ECM), and its major cell surface receptor, CD44, have been suggested to be important cellular mediators influencing tumor progression and treatment resistance in head and neck cancer. HNSCC contains a small subpopulation of cells that exhibit a hallmark of CD44-expressing cancer stem cell (CSC) properties with self-renewal, multipotency, and a unique potential for tumor initiation. HA has been shown to stimulate a variety of CSC functions including self-renewal, clone formation and differentiation. This review article will present current evidence for the existence of a unique small population of CD44v3
ALDH
-expressing CSCs in HNSCC. A special focus will be placed on the role of HA/CD44-induced oncogenic signaling and histone methyltransferase, DOT1L activities in regulating histone modifications (via epigenetic changes) and miRNA activation. Many of these events are essential for the CSC properties such as Nanog/Oct4/Sox2 expression, spheroid/clone formation, self-renewal, tumor cell migration/invasion, survival and chemotherapeutic drug resistance in HA-activated head and neck cancer. These newly-discovered HA/CD44-mediated oncogenic signaling pathways delineate unique tumor dynamics with implications for defining the drivers of HNSCC progression processes. Most importantly, the important knowledge obtained from HA/CD44-regulated CSC signaling and functional activation could provide new information regarding the design of novel drug targets to overcome current therapeutic drug resistance which will have significant treatment implications for head and neck cancer patients.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28837080</pmid><doi>10.3390/ijms18091849</doi><orcidid>https://orcid.org/0000-0003-3172-9251</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Activation Animals Biomarkers CD44 antigen Cell self-renewal Cell surface Chemoresistance Cloning Disease Progression Drug development Drug resistance Drug Resistance, Neoplasm - genetics Epigenesis, Genetic Epigenetics Extracellular Matrix Gene Expression Regulation, Neoplastic Head & neck cancer Head and Neck Neoplasms - genetics Head and Neck Neoplasms - metabolism Head and Neck Neoplasms - pathology Histone methyltransferase Histone-Lysine N-Methyltransferase - genetics Histone-Lysine N-Methyltransferase - metabolism Humans Hyaluronan Receptors - metabolism Hyaluronic acid Hyaluronic Acid - chemistry Hyaluronic Acid - metabolism Isoenzymes - metabolism Medical prognosis Metastases Methyltransferases - genetics Methyltransferases - metabolism MicroRNAs - genetics miRNA Molecular modelling Morbidity Neoplastic Stem Cells - drug effects Neoplastic Stem Cells - metabolism Oct-4 protein Patients Protein Binding Retinal Dehydrogenase - metabolism Review Signal Transduction Squamous cell carcinoma Stem cells Treatment resistance |
title | Activation of Matrix Hyaluronan-Mediated CD44 Signaling, Epigenetic Regulation and Chemoresistance in Head and Neck Cancer Stem Cells |
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