Preparation and pharmacological evaluation of norcantharidin-conjugated carboxymethyl chitosan in mice bearing hepatocellular carcinoma
•Carboxymethyl chitosan (CMCS) combined covalently onto norcantharidin (NCTD).•Orthotopic transplantation tumor model of hepatocellular carcinoma was established.•CMCS-NCTD was potent in anti-hepatoma and liver-protection effects in vivo. In this study, norcantharidin (NCTD), a small-molecule antica...
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creator | Jiang, Zhiwen Chi, Jinhua Han, Baoqin Liu, Wanshun |
description | •Carboxymethyl chitosan (CMCS) combined covalently onto norcantharidin (NCTD).•Orthotopic transplantation tumor model of hepatocellular carcinoma was established.•CMCS-NCTD was potent in anti-hepatoma and liver-protection effects in vivo.
In this study, norcantharidin (NCTD), a small-molecule anticancer drug derived from Chinese traditional medicine blister beetle (Mylabris), was conjugated covalently onto carboxymethyl chitosan (CMCS). Then the hepatocellular carcinoma therapeutic properties and liver-protective effects were investigated through orthotopic transplantation tumor model. Results showed that the obtained CMCS-NCTD demonstrated remarkable anti-growth efficacy against hepatocellular 22 in mice. Significant improvement of the liver injury caused by cancer cells was observed in tumor-bearing mice administrated with CMCS-NCTD. Moreover, CMCS-NCTD remarkably increased the serum levels of TNF-α, IFN-γ, TIMP-1 and E-cadherin in mice treated for 12days. Administration of CMCS-NCTD significantly reduced the elevated serum ALT, AST, VEGF and MMP-9 levels of tumor-bearing mice. In addition, activities of SOD and GSH-Px in serum or homogenate of the CMCS-NCTD treated mice were significantly high when compared with model control group. Our data suggested that CMCS-NCTD was a promising candidate as an anti-hepatoma and liver-protection compound. |
doi_str_mv | 10.1016/j.carbpol.2017.06.072 |
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In this study, norcantharidin (NCTD), a small-molecule anticancer drug derived from Chinese traditional medicine blister beetle (Mylabris), was conjugated covalently onto carboxymethyl chitosan (CMCS). Then the hepatocellular carcinoma therapeutic properties and liver-protective effects were investigated through orthotopic transplantation tumor model. Results showed that the obtained CMCS-NCTD demonstrated remarkable anti-growth efficacy against hepatocellular 22 in mice. Significant improvement of the liver injury caused by cancer cells was observed in tumor-bearing mice administrated with CMCS-NCTD. Moreover, CMCS-NCTD remarkably increased the serum levels of TNF-α, IFN-γ, TIMP-1 and E-cadherin in mice treated for 12days. Administration of CMCS-NCTD significantly reduced the elevated serum ALT, AST, VEGF and MMP-9 levels of tumor-bearing mice. In addition, activities of SOD and GSH-Px in serum or homogenate of the CMCS-NCTD treated mice were significantly high when compared with model control group. Our data suggested that CMCS-NCTD was a promising candidate as an anti-hepatoma and liver-protection compound.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2017.06.072</identifier><identifier>PMID: 28821069</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Anti-hepatoma ; Carboxymethyl chitosan ; Liver-protection ; Norcantharidin ; Orthotopic transplantation</subject><ispartof>Carbohydrate polymers, 2017-10, Vol.174, p.282-290</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-d7d23ce0f4be2dbbf7bb9bfe71dc9cde977a30d6ec0065ece67d256a56c263503</citedby><cites>FETCH-LOGICAL-c365t-d7d23ce0f4be2dbbf7bb9bfe71dc9cde977a30d6ec0065ece67d256a56c263503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0144861717306999$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28821069$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Zhiwen</creatorcontrib><creatorcontrib>Chi, Jinhua</creatorcontrib><creatorcontrib>Han, Baoqin</creatorcontrib><creatorcontrib>Liu, Wanshun</creatorcontrib><title>Preparation and pharmacological evaluation of norcantharidin-conjugated carboxymethyl chitosan in mice bearing hepatocellular carcinoma</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>•Carboxymethyl chitosan (CMCS) combined covalently onto norcantharidin (NCTD).•Orthotopic transplantation tumor model of hepatocellular carcinoma was established.•CMCS-NCTD was potent in anti-hepatoma and liver-protection effects in vivo.
In this study, norcantharidin (NCTD), a small-molecule anticancer drug derived from Chinese traditional medicine blister beetle (Mylabris), was conjugated covalently onto carboxymethyl chitosan (CMCS). Then the hepatocellular carcinoma therapeutic properties and liver-protective effects were investigated through orthotopic transplantation tumor model. Results showed that the obtained CMCS-NCTD demonstrated remarkable anti-growth efficacy against hepatocellular 22 in mice. Significant improvement of the liver injury caused by cancer cells was observed in tumor-bearing mice administrated with CMCS-NCTD. Moreover, CMCS-NCTD remarkably increased the serum levels of TNF-α, IFN-γ, TIMP-1 and E-cadherin in mice treated for 12days. Administration of CMCS-NCTD significantly reduced the elevated serum ALT, AST, VEGF and MMP-9 levels of tumor-bearing mice. In addition, activities of SOD and GSH-Px in serum or homogenate of the CMCS-NCTD treated mice were significantly high when compared with model control group. Our data suggested that CMCS-NCTD was a promising candidate as an anti-hepatoma and liver-protection compound.</description><subject>Anti-hepatoma</subject><subject>Carboxymethyl chitosan</subject><subject>Liver-protection</subject><subject>Norcantharidin</subject><subject>Orthotopic transplantation</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhi1ERZfCTwD5yCXBzoednBCqyodUiR7K2XLGk12vEjvYTsX-gv5tHO3CFV_m4PeZd2ZeQt5xVnLGxcdjCToMi5_KinFZMlEyWb0gO97JvuB107wkO8abpugEl9fkdYxHlp_g7BW5rrqu4kz0O_L8EHDRQSfrHdXO0OWgw6zBT35vQU8Un_S0nr_9SJ0PoF3KGmusK8C747rXCQ3dpvG_TzOmw2micLDJR-2odXS2gHTAjLg9PWS35AGnaZ102Ciwzs_6Dbka9RTx7aXekJ9f7h5vvxX3P75-v_18X0At2lQYaaoakI3NgJUZhlEOQz-MKLmBHgz2UuqaGYGQV20RUGSgFboVUIm6ZfUN-XDuuwT_a8WY1GzjNo526NeoeF-zpuOCiyxtz1IIPsaAo1qCnXU4Kc7UloE6qksGastAMaFyBpl7f7FYhxnNP-rv0bPg01mAedEni0FFsOgAjQ0ISRlv_2PxB5r4oD0</recordid><startdate>20171015</startdate><enddate>20171015</enddate><creator>Jiang, Zhiwen</creator><creator>Chi, Jinhua</creator><creator>Han, Baoqin</creator><creator>Liu, Wanshun</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20171015</creationdate><title>Preparation and pharmacological evaluation of norcantharidin-conjugated carboxymethyl chitosan in mice bearing hepatocellular carcinoma</title><author>Jiang, Zhiwen ; Chi, Jinhua ; Han, Baoqin ; Liu, Wanshun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-d7d23ce0f4be2dbbf7bb9bfe71dc9cde977a30d6ec0065ece67d256a56c263503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Anti-hepatoma</topic><topic>Carboxymethyl chitosan</topic><topic>Liver-protection</topic><topic>Norcantharidin</topic><topic>Orthotopic transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Zhiwen</creatorcontrib><creatorcontrib>Chi, Jinhua</creatorcontrib><creatorcontrib>Han, Baoqin</creatorcontrib><creatorcontrib>Liu, Wanshun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Zhiwen</au><au>Chi, Jinhua</au><au>Han, Baoqin</au><au>Liu, Wanshun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and pharmacological evaluation of norcantharidin-conjugated carboxymethyl chitosan in mice bearing hepatocellular carcinoma</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2017-10-15</date><risdate>2017</risdate><volume>174</volume><spage>282</spage><epage>290</epage><pages>282-290</pages><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>•Carboxymethyl chitosan (CMCS) combined covalently onto norcantharidin (NCTD).•Orthotopic transplantation tumor model of hepatocellular carcinoma was established.•CMCS-NCTD was potent in anti-hepatoma and liver-protection effects in vivo.
In this study, norcantharidin (NCTD), a small-molecule anticancer drug derived from Chinese traditional medicine blister beetle (Mylabris), was conjugated covalently onto carboxymethyl chitosan (CMCS). Then the hepatocellular carcinoma therapeutic properties and liver-protective effects were investigated through orthotopic transplantation tumor model. Results showed that the obtained CMCS-NCTD demonstrated remarkable anti-growth efficacy against hepatocellular 22 in mice. Significant improvement of the liver injury caused by cancer cells was observed in tumor-bearing mice administrated with CMCS-NCTD. Moreover, CMCS-NCTD remarkably increased the serum levels of TNF-α, IFN-γ, TIMP-1 and E-cadherin in mice treated for 12days. Administration of CMCS-NCTD significantly reduced the elevated serum ALT, AST, VEGF and MMP-9 levels of tumor-bearing mice. In addition, activities of SOD and GSH-Px in serum or homogenate of the CMCS-NCTD treated mice were significantly high when compared with model control group. Our data suggested that CMCS-NCTD was a promising candidate as an anti-hepatoma and liver-protection compound.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28821069</pmid><doi>10.1016/j.carbpol.2017.06.072</doi><tpages>9</tpages></addata></record> |
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subjects | Anti-hepatoma Carboxymethyl chitosan Liver-protection Norcantharidin Orthotopic transplantation |
title | Preparation and pharmacological evaluation of norcantharidin-conjugated carboxymethyl chitosan in mice bearing hepatocellular carcinoma |
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