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Triterpenoid saponin flaccidoside II from Anemone flaccida triggers apoptosis of NF1-associated malignant peripheral nerve sheath tumors via the MAPK-HO-1 pathway
Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive soft tissue neoplasms that are extremely rare and are frequently associated with neurofibromatosis type 1 patients. MPNSTs are typically fatal, and there is no effective treatment so far. In our previous study, we showed that fl...
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Published in: | OncoTargets and therapy 2016, Vol.9, p.1969-1979 |
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container_end_page | 1979 |
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container_start_page | 1969 |
container_title | OncoTargets and therapy |
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creator | Han, Lin-Tao Fang, Yin Cao, Yan Wu, Feng-Hua Liu, E Mo, Guo-Yan Huang, Fang |
description | Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive soft tissue neoplasms that are extremely rare and are frequently associated with neurofibromatosis type 1 patients. MPNSTs are typically fatal, and there is no effective treatment so far. In our previous study, we showed that flaccidoside II, one of the triterpenoid saponins isolated from Anemone flaccida Fr. Schmidt, has antitumor potential by inducing apoptosis. In the present study, we found that flaccidoside II inhibits proliferation and facilitates apoptosis in MPNST cell lines ST88-14 and S462. Furthermore, this study provides a mechanism by which the downregulation of heme oxygenase-1 via extracellular signal-regulated kinase-1/2 and p38 mitogen-activated protein kinase pathways is involved in the apoptotic role of flaccidoside II. This study suggested the potential of flaccidoside II as a novel pharmacotherapeutic approach for MPNSTs. |
doi_str_mv | 10.2147/OTT.S95597 |
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MPNSTs are typically fatal, and there is no effective treatment so far. In our previous study, we showed that flaccidoside II, one of the triterpenoid saponins isolated from Anemone flaccida Fr. Schmidt, has antitumor potential by inducing apoptosis. In the present study, we found that flaccidoside II inhibits proliferation and facilitates apoptosis in MPNST cell lines ST88-14 and S462. Furthermore, this study provides a mechanism by which the downregulation of heme oxygenase-1 via extracellular signal-regulated kinase-1/2 and p38 mitogen-activated protein kinase pathways is involved in the apoptotic role of flaccidoside II. This study suggested the potential of flaccidoside II as a novel pharmacotherapeutic approach for MPNSTs.</description><identifier>ISSN: 1178-6930</identifier><identifier>EISSN: 1178-6930</identifier><identifier>DOI: 10.2147/OTT.S95597</identifier><identifier>PMID: 27103823</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Alzheimer's disease ; Apoptosis ; Care and treatment ; Cell growth ; Cellular signal transduction ; Chemotherapy ; Development and progression ; Experiments ; Folk medicine ; Gene expression ; Genetic aspects ; Health aspects ; Kinases ; Neoplasia ; Nervous system ; Nervous system tumors ; Original Research ; Protein kinases ; Ranunculaceae ; Saponins ; Terpenoids ; Tumors</subject><ispartof>OncoTargets and therapy, 2016, Vol.9, p.1969-1979</ispartof><rights>COPYRIGHT 2016 Dove Medical Press Limited</rights><rights>2016. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Han et al. This work is published and licensed by Dove Medical Press Limited 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5177-3980730d1aee04004b3eb734496ea3765978a082b986306b21defe51797af1783</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2242718039/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2242718039?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,25753,27923,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27103823$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Lin-Tao</creatorcontrib><creatorcontrib>Fang, Yin</creatorcontrib><creatorcontrib>Cao, Yan</creatorcontrib><creatorcontrib>Wu, Feng-Hua</creatorcontrib><creatorcontrib>Liu, E</creatorcontrib><creatorcontrib>Mo, Guo-Yan</creatorcontrib><creatorcontrib>Huang, Fang</creatorcontrib><title>Triterpenoid saponin flaccidoside II from Anemone flaccida triggers apoptosis of NF1-associated malignant peripheral nerve sheath tumors via the MAPK-HO-1 pathway</title><title>OncoTargets and therapy</title><addtitle>Onco Targets Ther</addtitle><description>Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive soft tissue neoplasms that are extremely rare and are frequently associated with neurofibromatosis type 1 patients. 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subjects | Alzheimer's disease Apoptosis Care and treatment Cell growth Cellular signal transduction Chemotherapy Development and progression Experiments Folk medicine Gene expression Genetic aspects Health aspects Kinases Neoplasia Nervous system Nervous system tumors Original Research Protein kinases Ranunculaceae Saponins Terpenoids Tumors |
title | Triterpenoid saponin flaccidoside II from Anemone flaccida triggers apoptosis of NF1-associated malignant peripheral nerve sheath tumors via the MAPK-HO-1 pathway |
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