Divergent Synthesis of Chondroitin Sulfate Disaccharides and Identification of Sulfate Motifs that Inhibit Triple Negative Breast Cancer
Glycosaminoglycans (GAGs) regulate many important physiological processes. A pertinent issue to address is whether GAGs encode important functional information via introduction of position specific sulfate groups in the GAG structure. However, procurement of pure, homogenous GAG motifs to probe the...
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description | Glycosaminoglycans (GAGs) regulate many important physiological processes. A pertinent issue to address is whether GAGs encode important functional information via introduction of position specific sulfate groups in the GAG structure. However, procurement of pure, homogenous GAG motifs to probe the “sulfation code” is a challenging task due to isolation difficulty and structural complexity. To this end, we devised a versatile synthetic strategy to obtain all the 16 theoretically possible sulfation patterns in the chondroitin sulfate (CS) repeating unit; these include rare but potentially important sulfated motifs which have not been isolated earlier. Biological evaluation indicated that CS sulfation patterns had differing effects for different breast cancer cell types and the greatest inhibitory effect was observed for the most aggressive, triple negative breast cancer cell line MDA-MB-231. |
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A pertinent issue to address is whether GAGs encode important functional information via introduction of position specific sulfate groups in the GAG structure. However, procurement of pure, homogenous GAG motifs to probe the “sulfation code” is a challenging task due to isolation difficulty and structural complexity. To this end, we devised a versatile synthetic strategy to obtain all the 16 theoretically possible sulfation patterns in the chondroitin sulfate (CS) repeating unit; these include rare but potentially important sulfated motifs which have not been isolated earlier. Biological evaluation indicated that CS sulfation patterns had differing effects for different breast cancer cell types and the greatest inhibitory effect was observed for the most aggressive, triple negative breast cancer cell line MDA-MB-231.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep14355</identifier><identifier>PMID: 26400608</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/638 ; 639/638/549 ; 639/638/549/933 ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - pharmacology ; Berries ; Breast cancer ; Caspase 3 - metabolism ; Caspase 7 - metabolism ; Cell Line, Tumor ; Cell Survival - drug effects ; Chondroitin sulfate ; Chondroitin Sulfates - chemical synthesis ; Chondroitin Sulfates - pharmacology ; Disaccharides ; Enzyme Activation - drug effects ; Glycosaminoglycans ; Glycosylation ; Humanities and Social Sciences ; Humans ; Molecular Structure ; multidisciplinary ; Science ; Sulfates ; Triple Negative Breast Neoplasms</subject><ispartof>Scientific reports, 2015-09, Vol.5 (1), p.14355-14355, Article 14355</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Sep 2015</rights><rights>Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c578t-d50ca85bb8be69dad564975d172b7b382ab8431a773fcdf413c1ee26b40358263</citedby><cites>FETCH-LOGICAL-c578t-d50ca85bb8be69dad564975d172b7b382ab8431a773fcdf413c1ee26b40358263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155627/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155627/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26400608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wei Poh, Zhong</creatorcontrib><creatorcontrib>Heng Gan, Chin</creatorcontrib><creatorcontrib>Lee, Eric J.</creatorcontrib><creatorcontrib>Guo, Suxian</creatorcontrib><creatorcontrib>Yip, George W.</creatorcontrib><creatorcontrib>Lam, Yulin</creatorcontrib><title>Divergent Synthesis of Chondroitin Sulfate Disaccharides and Identification of Sulfate Motifs that Inhibit Triple Negative Breast Cancer</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Glycosaminoglycans (GAGs) regulate many important physiological processes. A pertinent issue to address is whether GAGs encode important functional information via introduction of position specific sulfate groups in the GAG structure. However, procurement of pure, homogenous GAG motifs to probe the “sulfation code” is a challenging task due to isolation difficulty and structural complexity. To this end, we devised a versatile synthetic strategy to obtain all the 16 theoretically possible sulfation patterns in the chondroitin sulfate (CS) repeating unit; these include rare but potentially important sulfated motifs which have not been isolated earlier. Biological evaluation indicated that CS sulfation patterns had differing effects for different breast cancer cell types and the greatest inhibitory effect was observed for the most aggressive, triple negative breast cancer cell line MDA-MB-231.</description><subject>639/638</subject><subject>639/638/549</subject><subject>639/638/549/933</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Berries</subject><subject>Breast cancer</subject><subject>Caspase 3 - metabolism</subject><subject>Caspase 7 - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Chondroitin sulfate</subject><subject>Chondroitin Sulfates - chemical synthesis</subject><subject>Chondroitin Sulfates - pharmacology</subject><subject>Disaccharides</subject><subject>Enzyme Activation - drug effects</subject><subject>Glycosaminoglycans</subject><subject>Glycosylation</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Molecular Structure</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Sulfates</subject><subject>Triple Negative Breast Neoplasms</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNplkc9uGyEQxlHVqonSHPoCFVIvbSS3wC4Le6nUOv1jKU0OSc-IhVkv0RpcYC3lDfLYxXJiuclcGDG_-WZGH0JvKflESSU_pwhrWlecv0DHjNR8xirGXh7kR-g0pVtSgrO2pu1rdMSampCGyGN0f-42EJfgM76-83mA5BIOPZ4PwdsYXHYeX09jrzPgc5e0MYOOzkLC2lu8sKXR9c7o7ILf9j2yv0P5TzgPOuOFH1znMr6Jbj0CvoRlwTeAv0XQKeO59gbiG_Sq12OC04f3BP358f1m_mt2cfVzMf96MTNcyDyznBgtedfJDprWasubuhXcUsE60VWS6U7WFdVCVL2xfU0rQwFY09Wk4pI11Qn6stNdT90KrCkHRD2qdXQrHe9U0E79X_FuUMuwUZxy3jBRBD48CMTwd4KU1colA-OoPYQpKSqoJEIKTgr6_gl6G6boy3mKyrYVDW-bLfVxR5kYUnGz3y9DidparPYWF_bd4fZ78tHQApztgFRKfgnxYOQztX95fbJv</recordid><startdate>20150924</startdate><enddate>20150924</enddate><creator>Wei Poh, Zhong</creator><creator>Heng Gan, Chin</creator><creator>Lee, Eric J.</creator><creator>Guo, Suxian</creator><creator>Yip, George W.</creator><creator>Lam, Yulin</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150924</creationdate><title>Divergent Synthesis of Chondroitin Sulfate Disaccharides and Identification of Sulfate Motifs that Inhibit Triple Negative Breast Cancer</title><author>Wei Poh, Zhong ; Heng Gan, Chin ; Lee, Eric J. ; Guo, Suxian ; Yip, George W. ; Lam, Yulin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c578t-d50ca85bb8be69dad564975d172b7b382ab8431a773fcdf413c1ee26b40358263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>639/638</topic><topic>639/638/549</topic><topic>639/638/549/933</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Berries</topic><topic>Breast cancer</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase 7 - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>Chondroitin sulfate</topic><topic>Chondroitin Sulfates - chemical synthesis</topic><topic>Chondroitin Sulfates - pharmacology</topic><topic>Disaccharides</topic><topic>Enzyme Activation - drug effects</topic><topic>Glycosaminoglycans</topic><topic>Glycosylation</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Molecular Structure</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Sulfates</topic><topic>Triple Negative Breast Neoplasms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei Poh, Zhong</creatorcontrib><creatorcontrib>Heng Gan, Chin</creatorcontrib><creatorcontrib>Lee, Eric J.</creatorcontrib><creatorcontrib>Guo, Suxian</creatorcontrib><creatorcontrib>Yip, George W.</creatorcontrib><creatorcontrib>Lam, Yulin</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei Poh, Zhong</au><au>Heng Gan, Chin</au><au>Lee, Eric J.</au><au>Guo, Suxian</au><au>Yip, George W.</au><au>Lam, Yulin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergent Synthesis of Chondroitin Sulfate Disaccharides and Identification of Sulfate Motifs that Inhibit Triple Negative Breast Cancer</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-09-24</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>14355</spage><epage>14355</epage><pages>14355-14355</pages><artnum>14355</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Glycosaminoglycans (GAGs) regulate many important physiological processes. A pertinent issue to address is whether GAGs encode important functional information via introduction of position specific sulfate groups in the GAG structure. However, procurement of pure, homogenous GAG motifs to probe the “sulfation code” is a challenging task due to isolation difficulty and structural complexity. To this end, we devised a versatile synthetic strategy to obtain all the 16 theoretically possible sulfation patterns in the chondroitin sulfate (CS) repeating unit; these include rare but potentially important sulfated motifs which have not been isolated earlier. Biological evaluation indicated that CS sulfation patterns had differing effects for different breast cancer cell types and the greatest inhibitory effect was observed for the most aggressive, triple negative breast cancer cell line MDA-MB-231.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26400608</pmid><doi>10.1038/srep14355</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 639/638 639/638/549 639/638/549/933 Antineoplastic Agents - chemical synthesis Antineoplastic Agents - pharmacology Berries Breast cancer Caspase 3 - metabolism Caspase 7 - metabolism Cell Line, Tumor Cell Survival - drug effects Chondroitin sulfate Chondroitin Sulfates - chemical synthesis Chondroitin Sulfates - pharmacology Disaccharides Enzyme Activation - drug effects Glycosaminoglycans Glycosylation Humanities and Social Sciences Humans Molecular Structure multidisciplinary Science Sulfates Triple Negative Breast Neoplasms |
title | Divergent Synthesis of Chondroitin Sulfate Disaccharides and Identification of Sulfate Motifs that Inhibit Triple Negative Breast Cancer |
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