β-elemene inhibits radiation and hypoxia-induced macrophages infiltration via Prx-1/NF-κB/HIF-1α signaling pathway
: In cancers, tumor-associated macrophages (TAMs) play an important role in the progression, evasion of immunity and sensitivity to therapy. Unfortunately, radiation and hypoxia could induce the M2 macrophages infiltration and polarization. In this study, we investigated the relevance of macrophage...
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Veröffentlicht in: | OncoTargets and therapy 2019-01, Vol.12, p.4203-4211 |
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creator | Yu, Xiaomu Li, Zongjuan Zhang, Yang Xu, Maoyi Che, Yilin Tian, Xiaoyuan Wang, Ruonan Zou, Kun Zou, Lijuan |
description | : In cancers, tumor-associated macrophages (TAMs) play an important role in the progression, evasion of immunity and sensitivity to therapy. Unfortunately, radiation and hypoxia could induce the M2 macrophages infiltration and polarization.
In this study, we investigated the relevance of macrophage recruitment with radiation and hypoxia by transwell. We also evaluated the effect of β-elemene on the infiltration of M2 macrophages and explored its underlying molecular mechanism by a series of in vitro and in vivo experiments.
Irradiated or hypoxia lung cancer cells recruit macrophages, and the recruitment is MCP-1 dependent. We also found that radiation and hypoxia-induced MCP-1 secretion follows upregulation of Prx-1, which leads to nuclear accumulation of NF-κB and HIF-1α expression. In addition, β-elemene could effectively suppress this recruitment phenomenon through Prx-1/NF-κB/HIF-1α signaling.
Our study showed that radiation and hypoxia significantly promoted the macrophages recruitment. β-elemene could effectively suppress this recruitment phenomenon and MCP-1 expression via inhibiting Prx-1/NF-κB/HIF-1α pathways. |
doi_str_mv | 10.2147/OTT.S196910 |
format | Article |
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In this study, we investigated the relevance of macrophage recruitment with radiation and hypoxia by transwell. We also evaluated the effect of β-elemene on the infiltration of M2 macrophages and explored its underlying molecular mechanism by a series of in vitro and in vivo experiments.
Irradiated or hypoxia lung cancer cells recruit macrophages, and the recruitment is MCP-1 dependent. We also found that radiation and hypoxia-induced MCP-1 secretion follows upregulation of Prx-1, which leads to nuclear accumulation of NF-κB and HIF-1α expression. In addition, β-elemene could effectively suppress this recruitment phenomenon through Prx-1/NF-κB/HIF-1α signaling.
Our study showed that radiation and hypoxia significantly promoted the macrophages recruitment. β-elemene could effectively suppress this recruitment phenomenon and MCP-1 expression via inhibiting Prx-1/NF-κB/HIF-1α pathways.</description><identifier>ISSN: 1178-6930</identifier><identifier>EISSN: 1178-6930</identifier><identifier>DOI: 10.2147/OTT.S196910</identifier><identifier>PMID: 31213838</identifier><language>eng</language><publisher>New Zealand: Dove</publisher><subject>Original Research</subject><ispartof>OncoTargets and therapy, 2019-01, Vol.12, p.4203-4211</ispartof><rights>2019 Yu et al. 2019 Yu et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-4301f337e8fbad70e24d02ec79402394ddec13b0c0ec030b3b219681654d68ef3</citedby><orcidid>0000-0001-6331-5323</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/PMC6549424/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549424/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3848,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31213838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Xiaomu</creatorcontrib><creatorcontrib>Li, Zongjuan</creatorcontrib><creatorcontrib>Zhang, Yang</creatorcontrib><creatorcontrib>Xu, Maoyi</creatorcontrib><creatorcontrib>Che, Yilin</creatorcontrib><creatorcontrib>Tian, Xiaoyuan</creatorcontrib><creatorcontrib>Wang, Ruonan</creatorcontrib><creatorcontrib>Zou, Kun</creatorcontrib><creatorcontrib>Zou, Lijuan</creatorcontrib><title>β-elemene inhibits radiation and hypoxia-induced macrophages infiltration via Prx-1/NF-κB/HIF-1α signaling pathway</title><title>OncoTargets and therapy</title><addtitle>Onco Targets Ther</addtitle><description>: In cancers, tumor-associated macrophages (TAMs) play an important role in the progression, evasion of immunity and sensitivity to therapy. Unfortunately, radiation and hypoxia could induce the M2 macrophages infiltration and polarization.
In this study, we investigated the relevance of macrophage recruitment with radiation and hypoxia by transwell. We also evaluated the effect of β-elemene on the infiltration of M2 macrophages and explored its underlying molecular mechanism by a series of in vitro and in vivo experiments.
Irradiated or hypoxia lung cancer cells recruit macrophages, and the recruitment is MCP-1 dependent. We also found that radiation and hypoxia-induced MCP-1 secretion follows upregulation of Prx-1, which leads to nuclear accumulation of NF-κB and HIF-1α expression. In addition, β-elemene could effectively suppress this recruitment phenomenon through Prx-1/NF-κB/HIF-1α signaling.
Our study showed that radiation and hypoxia significantly promoted the macrophages recruitment. β-elemene could effectively suppress this recruitment phenomenon and MCP-1 expression via inhibiting Prx-1/NF-κB/HIF-1α pathways.</description><subject>Original Research</subject><issn>1178-6930</issn><issn>1178-6930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkU1LxDAQhoMofp-8S4-CxM2X_bgIKq4KooLrOaTJdBtp09q06v4sPfoj9jcZ2VX0NAPzzDsv8yK0R8kRoyIZ3U0mRw80izNKVtAmpUmK44yT1T_9Btry_omQOE6ZWEcbnDLKU55uomH-gaGCGhxE1pU2t72POmWs6m3jIuVMVM7a5s0qbJ0ZNJioVrpr2lJNwYeVwlZ9t4BfrIruuzdMR7djPP88G11djzGdv0feTp2qrJtGrerLVzXbQWuFqjzsLus2ehxfTM6v8M3d5fX56Q3WgvEeC05owXkCaZErkxBgwhAGOskEYTwTxoCmPCeagCac5Dxn4Q8pjY-FiVMo-DY6Wei2Q16D0eCC10q2na1VN5ONsvL_xNlSTpsXGRQywUQQOFgKdM3zAL6XtfUaqko5aAYvWWBEGsf8Gz1coOE73ndQ_J6hRH4HJUNQchlUoPf_Ovtlf5LhX_vEkiM</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Yu, Xiaomu</creator><creator>Li, Zongjuan</creator><creator>Zhang, Yang</creator><creator>Xu, Maoyi</creator><creator>Che, Yilin</creator><creator>Tian, Xiaoyuan</creator><creator>Wang, Ruonan</creator><creator>Zou, Kun</creator><creator>Zou, Lijuan</creator><general>Dove</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6331-5323</orcidid></search><sort><creationdate>20190101</creationdate><title>β-elemene inhibits radiation and hypoxia-induced macrophages infiltration via Prx-1/NF-κB/HIF-1α signaling pathway</title><author>Yu, Xiaomu ; Li, Zongjuan ; Zhang, Yang ; Xu, Maoyi ; Che, Yilin ; Tian, Xiaoyuan ; Wang, Ruonan ; Zou, Kun ; Zou, Lijuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-4301f337e8fbad70e24d02ec79402394ddec13b0c0ec030b3b219681654d68ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Original Research</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Xiaomu</creatorcontrib><creatorcontrib>Li, Zongjuan</creatorcontrib><creatorcontrib>Zhang, Yang</creatorcontrib><creatorcontrib>Xu, Maoyi</creatorcontrib><creatorcontrib>Che, Yilin</creatorcontrib><creatorcontrib>Tian, Xiaoyuan</creatorcontrib><creatorcontrib>Wang, Ruonan</creatorcontrib><creatorcontrib>Zou, Kun</creatorcontrib><creatorcontrib>Zou, Lijuan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>OncoTargets and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Xiaomu</au><au>Li, Zongjuan</au><au>Zhang, Yang</au><au>Xu, Maoyi</au><au>Che, Yilin</au><au>Tian, Xiaoyuan</au><au>Wang, Ruonan</au><au>Zou, Kun</au><au>Zou, Lijuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β-elemene inhibits radiation and hypoxia-induced macrophages infiltration via Prx-1/NF-κB/HIF-1α signaling pathway</atitle><jtitle>OncoTargets and therapy</jtitle><addtitle>Onco Targets Ther</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>12</volume><spage>4203</spage><epage>4211</epage><pages>4203-4211</pages><issn>1178-6930</issn><eissn>1178-6930</eissn><abstract>: In cancers, tumor-associated macrophages (TAMs) play an important role in the progression, evasion of immunity and sensitivity to therapy. Unfortunately, radiation and hypoxia could induce the M2 macrophages infiltration and polarization.
In this study, we investigated the relevance of macrophage recruitment with radiation and hypoxia by transwell. We also evaluated the effect of β-elemene on the infiltration of M2 macrophages and explored its underlying molecular mechanism by a series of in vitro and in vivo experiments.
Irradiated or hypoxia lung cancer cells recruit macrophages, and the recruitment is MCP-1 dependent. We also found that radiation and hypoxia-induced MCP-1 secretion follows upregulation of Prx-1, which leads to nuclear accumulation of NF-κB and HIF-1α expression. In addition, β-elemene could effectively suppress this recruitment phenomenon through Prx-1/NF-κB/HIF-1α signaling.
Our study showed that radiation and hypoxia significantly promoted the macrophages recruitment. β-elemene could effectively suppress this recruitment phenomenon and MCP-1 expression via inhibiting Prx-1/NF-κB/HIF-1α pathways.</abstract><cop>New Zealand</cop><pub>Dove</pub><pmid>31213838</pmid><doi>10.2147/OTT.S196910</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6331-5323</orcidid><oa>free_for_read</oa></addata></record> |
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source | Taylor & Francis Open Access; DOVE Medical Press Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; PubMed Central |
subjects | Original Research |
title | β-elemene inhibits radiation and hypoxia-induced macrophages infiltration via Prx-1/NF-κB/HIF-1α signaling pathway |
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