New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii
Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and...
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Veröffentlicht in: | Fitoterapia 2018-10, Vol.130, p.281-289 |
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description | Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy.
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doi_str_mv | 10.1016/j.fitote.2018.09.008 |
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[Display omitted]</description><identifier>ISSN: 0367-326X</identifier><identifier>EISSN: 1873-6971</identifier><identifier>DOI: 10.1016/j.fitote.2018.09.008</identifier><identifier>PMID: 30240842</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anticancer activity ; Cancer ; Cancer therapies ; Cytotoxicity ; Enantiomers ; Gelatinase B ; Lignans ; Matrix metalloproteinase ; Matrix metalloproteinases ; Metalloproteinase ; Metastases ; Metastasis ; Migration ; Molecular docking ; Optical activity ; Selaginella moellendorffii ; Structure-activity relationships ; Surface plasmon resonance ; Therapy ; Toxicity ; Tumor cell lines ; Tumors ; Zinc</subject><ispartof>Fitoterapia, 2018-10, Vol.130, p.281-289</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Oct 2018</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</citedby><cites>FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fitote.2018.09.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30240842$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yuan</creatorcontrib><creatorcontrib>Huang, Ri-Zhen</creatorcontrib><creatorcontrib>Wang, Chun-Gu</creatorcontrib><creatorcontrib>Ouyang, Xi-Lin</creatorcontrib><creatorcontrib>Jing, Xiao-Teng</creatorcontrib><creatorcontrib>Liang, Dong</creatorcontrib><creatorcontrib>Wang, Heng-Shan</creatorcontrib><title>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</title><title>Fitoterapia</title><addtitle>Fitoterapia</addtitle><description>Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy.
[Display omitted]</description><subject>Anticancer activity</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cytotoxicity</subject><subject>Enantiomers</subject><subject>Gelatinase B</subject><subject>Lignans</subject><subject>Matrix metalloproteinase</subject><subject>Matrix metalloproteinases</subject><subject>Metalloproteinase</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Migration</subject><subject>Molecular docking</subject><subject>Optical activity</subject><subject>Selaginella moellendorffii</subject><subject>Structure-activity relationships</subject><subject>Surface plasmon resonance</subject><subject>Therapy</subject><subject>Toxicity</subject><subject>Tumor cell lines</subject><subject>Tumors</subject><subject>Zinc</subject><issn>0367-326X</issn><issn>1873-6971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kMlKLDEUhoNc0XZ4A7kE7kYXVZ4kNboQRJygHUAFV4ZU6kTTVFXapNrh7Y2016Wrs_mn8xGywyBlwIr9WWrs6EZMObAqhToFqFbIhFWlSIq6ZH_IBERRJoIXD-tkI4QZAMtFxtbIugCeQZXxCXm8wjdqh2fbxDAfqDO0V6O377THUXWdm_vYYQcVMNCa7l5e3iT13gGd2qdBDYEa73p6i516sgN2naK9iweH1nljrN0iq0Z1Abe_7ya5Pz25Oz5PptdnF8dH00RneTHGvQprUWLVIuqmYGUmUJeMG4Wt4GVeN5rnvNAmbzJTN5CpBqDVVaPKAkRlxCb5t8yNc18WGEY5cws_xErJmWCViFR4VGVLlfYuBI9Gzr3tlf-QDOQXVDmTS6jyC6qEWkao0fb3O3zR9Nj-mP5TjILDpQDji68WvQza4qCxtR71KFtnf2_4BAjjir0</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Zhu, Yuan</creator><creator>Huang, Ri-Zhen</creator><creator>Wang, Chun-Gu</creator><creator>Ouyang, Xi-Lin</creator><creator>Jing, Xiao-Teng</creator><creator>Liang, Dong</creator><creator>Wang, Heng-Shan</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20181001</creationdate><title>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</title><author>Zhu, Yuan ; Huang, Ri-Zhen ; Wang, Chun-Gu ; Ouyang, Xi-Lin ; Jing, Xiao-Teng ; Liang, Dong ; Wang, Heng-Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anticancer activity</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Cytotoxicity</topic><topic>Enantiomers</topic><topic>Gelatinase B</topic><topic>Lignans</topic><topic>Matrix metalloproteinase</topic><topic>Matrix metalloproteinases</topic><topic>Metalloproteinase</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Migration</topic><topic>Molecular docking</topic><topic>Optical activity</topic><topic>Selaginella moellendorffii</topic><topic>Structure-activity relationships</topic><topic>Surface plasmon resonance</topic><topic>Therapy</topic><topic>Toxicity</topic><topic>Tumor cell lines</topic><topic>Tumors</topic><topic>Zinc</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yuan</creatorcontrib><creatorcontrib>Huang, Ri-Zhen</creatorcontrib><creatorcontrib>Wang, Chun-Gu</creatorcontrib><creatorcontrib>Ouyang, Xi-Lin</creatorcontrib><creatorcontrib>Jing, Xiao-Teng</creatorcontrib><creatorcontrib>Liang, Dong</creatorcontrib><creatorcontrib>Wang, Heng-Shan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Fitoterapia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Yuan</au><au>Huang, Ri-Zhen</au><au>Wang, Chun-Gu</au><au>Ouyang, Xi-Lin</au><au>Jing, Xiao-Teng</au><au>Liang, Dong</au><au>Wang, Heng-Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</atitle><jtitle>Fitoterapia</jtitle><addtitle>Fitoterapia</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>130</volume><spage>281</spage><epage>289</epage><pages>281-289</pages><issn>0367-326X</issn><eissn>1873-6971</eissn><abstract>Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy.
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subjects | Anticancer activity Cancer Cancer therapies Cytotoxicity Enantiomers Gelatinase B Lignans Matrix metalloproteinase Matrix metalloproteinases Metalloproteinase Metastases Metastasis Migration Molecular docking Optical activity Selaginella moellendorffii Structure-activity relationships Surface plasmon resonance Therapy Toxicity Tumor cell lines Tumors Zinc |
title | New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii |
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