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Astragalus Polysaccharides Inhibits Tumorigenesis and Lipid Metabolism Through miR-138-5p/SIRT1/SREBP1 Pathway in Prostate Cancer
polysaccharides (APS) is a traditional Chinese medicine and have been proved to involve in multiple biological processes, including inflammation, metabolism, and carcinogenics. However, the specific mechanisms by which APS on prostate cancer (PCa) remains largely unknown. In the current study, we fo...
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Published in: | Frontiers in pharmacology 2020-05, Vol.11, p.598-598 |
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description | polysaccharides (APS) is a traditional Chinese medicine and have been proved to involve in multiple biological processes, including inflammation, metabolism, and carcinogenics. However, the specific mechanisms by which APS on prostate cancer (PCa) remains largely unknown. In the current study, we found APS greatly inhibited the proliferation and invasion of PCa cells in a dose-dependent and time-dependent manner
and
. In addition, cellular triglyceride and cholesterol levels were also decreased significantly under APS treatment. Microarray data revealed the SIRT1 expression was markably suppressed under APS exposure. Mechanistic studies demonstrated that over-expression of SIRT1 inhibits the expression and nuclear translocation of SREBP1
activating AMPK phosphorylation to suppress lipid metabolism. Otherwise, knockdown of SIRT1 significantly promotes AMPK/SREBP1 signaling and its associated target genes. Besides, we also found miR-138-5p was greatly inhibited the SIRT1 expression to regulating cell metabolism by targeting its 3'UTR region. To summarize, our findings suggested that APS inhibits tumorigenesis and lipid metabolism through miR-138-5p/SIRT1/SREBP1 pathways in PCa. |
doi_str_mv | 10.3389/fphar.2020.00598 |
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and
. In addition, cellular triglyceride and cholesterol levels were also decreased significantly under APS treatment. Microarray data revealed the SIRT1 expression was markably suppressed under APS exposure. Mechanistic studies demonstrated that over-expression of SIRT1 inhibits the expression and nuclear translocation of SREBP1
activating AMPK phosphorylation to suppress lipid metabolism. Otherwise, knockdown of SIRT1 significantly promotes AMPK/SREBP1 signaling and its associated target genes. Besides, we also found miR-138-5p was greatly inhibited the SIRT1 expression to regulating cell metabolism by targeting its 3'UTR region. To summarize, our findings suggested that APS inhibits tumorigenesis and lipid metabolism through miR-138-5p/SIRT1/SREBP1 pathways in PCa.</description><identifier>ISSN: 1663-9812</identifier><identifier>EISSN: 1663-9812</identifier><identifier>DOI: 10.3389/fphar.2020.00598</identifier><identifier>PMID: 32431616</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Astragalus polysaccharides ; miRNA-138-5p ; Pharmacology ; prostate cancer ; SIRT1 ; SREBP1</subject><ispartof>Frontiers in pharmacology, 2020-05, Vol.11, p.598-598</ispartof><rights>Copyright © 2020 Guo, Ma, Jiang, Li and Jia.</rights><rights>Copyright © 2020 Guo, Ma, Jiang, Li and Jia 2020 Guo, Ma, Jiang, Li and Jia</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-9cc20dc9a76f27fa9338914e4b24010ece35bb51581df4dd1b1bbe6aa4bddad33</citedby><cites>FETCH-LOGICAL-c462t-9cc20dc9a76f27fa9338914e4b24010ece35bb51581df4dd1b1bbe6aa4bddad33</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/PMC7214922/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214922/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32431616$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Shanqi</creatorcontrib><creatorcontrib>Ma, Baojie</creatorcontrib><creatorcontrib>Jiang, Xingkang</creatorcontrib><creatorcontrib>Li, Xiaojiang</creatorcontrib><creatorcontrib>Jia, Yingjie</creatorcontrib><title>Astragalus Polysaccharides Inhibits Tumorigenesis and Lipid Metabolism Through miR-138-5p/SIRT1/SREBP1 Pathway in Prostate Cancer</title><title>Frontiers in pharmacology</title><addtitle>Front Pharmacol</addtitle><description>polysaccharides (APS) is a traditional Chinese medicine and have been proved to involve in multiple biological processes, including inflammation, metabolism, and carcinogenics. However, the specific mechanisms by which APS on prostate cancer (PCa) remains largely unknown. In the current study, we found APS greatly inhibited the proliferation and invasion of PCa cells in a dose-dependent and time-dependent manner
and
. In addition, cellular triglyceride and cholesterol levels were also decreased significantly under APS treatment. Microarray data revealed the SIRT1 expression was markably suppressed under APS exposure. Mechanistic studies demonstrated that over-expression of SIRT1 inhibits the expression and nuclear translocation of SREBP1
activating AMPK phosphorylation to suppress lipid metabolism. Otherwise, knockdown of SIRT1 significantly promotes AMPK/SREBP1 signaling and its associated target genes. Besides, we also found miR-138-5p was greatly inhibited the SIRT1 expression to regulating cell metabolism by targeting its 3'UTR region. To summarize, our findings suggested that APS inhibits tumorigenesis and lipid metabolism through miR-138-5p/SIRT1/SREBP1 pathways in PCa.</description><subject>Astragalus polysaccharides</subject><subject>miRNA-138-5p</subject><subject>Pharmacology</subject><subject>prostate cancer</subject><subject>SIRT1</subject><subject>SREBP1</subject><issn>1663-9812</issn><issn>1663-9812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkj1v2zAQhoWiRROk2TsVHLvI5pdkaSmQGmlqwEUNx52JI3mSGEiiS0otPPafR7bTIOFCgnf3HO_lmyQfGZ0JUZTzat9AmHHK6YzSrCzeJJcsz0VaFoy_fXG-SK5jfKDTEmUpcvk-uRBcCpaz_DL5dxOHADW0YyQb3x4iGDNhncVIVn3jtBsi2Y2dD67GHqOLBHpL1m7vLPmBA2jfutiRXRP8WDekc9uUiSLN9vP71XbH5vfb268bRjYwNH_hQFxPNsHHAQYkS-gNhg_JuwraiNdP-1Xy69vtbvk9Xf-8Wy1v1qmROR_S0hhOrSlhkVd8UUF51IBJlJpLyigaFJnWGcsKZitpLdNMa8wBpLYWrBBXyerMtR4e1D64DsJBeXDqdOFDrSAMzrSomGCaa8swx0JSyossyzkHRjNtBfLFxPpyZu1H3aE12E8itq-gryO9a1Tt_6gFZ7LkfAJ8fgIE_3vEOKjORYNtCz36MapppkxQObWaUuk51Uy6xYDVcxtG1VEEdTKCOhpBnYwwlXx6-bzngv_fLh4BXvCwjA</recordid><startdate>20200505</startdate><enddate>20200505</enddate><creator>Guo, Shanqi</creator><creator>Ma, Baojie</creator><creator>Jiang, Xingkang</creator><creator>Li, Xiaojiang</creator><creator>Jia, Yingjie</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20200505</creationdate><title>Astragalus Polysaccharides Inhibits Tumorigenesis and Lipid Metabolism Through miR-138-5p/SIRT1/SREBP1 Pathway in Prostate Cancer</title><author>Guo, Shanqi ; Ma, Baojie ; Jiang, Xingkang ; Li, Xiaojiang ; Jia, Yingjie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-9cc20dc9a76f27fa9338914e4b24010ece35bb51581df4dd1b1bbe6aa4bddad33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Astragalus polysaccharides</topic><topic>miRNA-138-5p</topic><topic>Pharmacology</topic><topic>prostate cancer</topic><topic>SIRT1</topic><topic>SREBP1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Shanqi</creatorcontrib><creatorcontrib>Ma, Baojie</creatorcontrib><creatorcontrib>Jiang, Xingkang</creatorcontrib><creatorcontrib>Li, Xiaojiang</creatorcontrib><creatorcontrib>Jia, Yingjie</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Shanqi</au><au>Ma, Baojie</au><au>Jiang, Xingkang</au><au>Li, Xiaojiang</au><au>Jia, Yingjie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Astragalus Polysaccharides Inhibits Tumorigenesis and Lipid Metabolism Through miR-138-5p/SIRT1/SREBP1 Pathway in Prostate Cancer</atitle><jtitle>Frontiers in pharmacology</jtitle><addtitle>Front Pharmacol</addtitle><date>2020-05-05</date><risdate>2020</risdate><volume>11</volume><spage>598</spage><epage>598</epage><pages>598-598</pages><issn>1663-9812</issn><eissn>1663-9812</eissn><abstract>polysaccharides (APS) is a traditional Chinese medicine and have been proved to involve in multiple biological processes, including inflammation, metabolism, and carcinogenics. However, the specific mechanisms by which APS on prostate cancer (PCa) remains largely unknown. In the current study, we found APS greatly inhibited the proliferation and invasion of PCa cells in a dose-dependent and time-dependent manner
and
. In addition, cellular triglyceride and cholesterol levels were also decreased significantly under APS treatment. Microarray data revealed the SIRT1 expression was markably suppressed under APS exposure. Mechanistic studies demonstrated that over-expression of SIRT1 inhibits the expression and nuclear translocation of SREBP1
activating AMPK phosphorylation to suppress lipid metabolism. Otherwise, knockdown of SIRT1 significantly promotes AMPK/SREBP1 signaling and its associated target genes. Besides, we also found miR-138-5p was greatly inhibited the SIRT1 expression to regulating cell metabolism by targeting its 3'UTR region. To summarize, our findings suggested that APS inhibits tumorigenesis and lipid metabolism through miR-138-5p/SIRT1/SREBP1 pathways in PCa.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>32431616</pmid><doi>10.3389/fphar.2020.00598</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Astragalus polysaccharides miRNA-138-5p Pharmacology prostate cancer SIRT1 SREBP1 |
title | Astragalus Polysaccharides Inhibits Tumorigenesis and Lipid Metabolism Through miR-138-5p/SIRT1/SREBP1 Pathway in Prostate Cancer |
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