Berberine, a natural compound, suppresses Hedgehog signaling pathway activity and cancer growth
Berberine (BBR), a natural alkaloid compound, is used as a non-prescription drug in China for treating diarrhea and gastroenteritis. Many studies have revealed that BBR possesses anticancer effect. However, the molecular mechanisms underlying its anticancer action is far from being fully elucidated....
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description | Berberine (BBR), a natural alkaloid compound, is used as a non-prescription drug in China for treating diarrhea and gastroenteritis. Many studies have revealed that BBR possesses anticancer effect. However, the molecular mechanisms underlying its anticancer action is far from being fully elucidated. This study is aimed to determine the effect of BBR on the hedgehog (Hh) activity and the growth of cancers addiction to Hh activity.
The Hh activity was determined by dual luciferase assays and quantitative RT-PCR analyses. The growth inhibition of BBR on medulloblastoma which was obtained from ptch+/-;p53-/- mice was analyzed by 5-bromo-2-deoxyuridine (Brdu) assays and by allografting the medulloblastoma into nude mice. The data were statistically analyzed by one-way analysis of variance (ANOVA), and multiple comparison between the groups was performed using Dunnett's method.
In this study, we found that BBR significantly inhibited the Hh pathway activity. Meanwhile, we observed that BBR failed to affect the transcriptional factors activities provoked by tumor necrosis factor-α (TNF-α) and Prostaglandin E2 (PGE2), thus suggesting its unique property against Hh pathway activity. Further studies revealed that BBR inhibited the Hh pathway activity by potentially targeting the critical component Smoothened (Smo) and most likely shared the same binding site on Smo with cyclopamine, a classical Smo inhibitor. Finally, we demonstrated that BBR obviously suppressed the Hh-dependent medulloblastoma growth in vitro and in vivo.
Collectively, our study uncovered a novel molecular mechanism responsible for the anticancer action of BBR, thus opening the way for the usage of BBR for therapeutics of cancers addiction to aberrant Hh pathway activity. |
doi_str_mv | 10.1186/s12885-015-1596-z |
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The Hh activity was determined by dual luciferase assays and quantitative RT-PCR analyses. The growth inhibition of BBR on medulloblastoma which was obtained from ptch+/-;p53-/- mice was analyzed by 5-bromo-2-deoxyuridine (Brdu) assays and by allografting the medulloblastoma into nude mice. The data were statistically analyzed by one-way analysis of variance (ANOVA), and multiple comparison between the groups was performed using Dunnett's method.
In this study, we found that BBR significantly inhibited the Hh pathway activity. Meanwhile, we observed that BBR failed to affect the transcriptional factors activities provoked by tumor necrosis factor-α (TNF-α) and Prostaglandin E2 (PGE2), thus suggesting its unique property against Hh pathway activity. Further studies revealed that BBR inhibited the Hh pathway activity by potentially targeting the critical component Smoothened (Smo) and most likely shared the same binding site on Smo with cyclopamine, a classical Smo inhibitor. Finally, we demonstrated that BBR obviously suppressed the Hh-dependent medulloblastoma growth in vitro and in vivo.
Collectively, our study uncovered a novel molecular mechanism responsible for the anticancer action of BBR, thus opening the way for the usage of BBR for therapeutics of cancers addiction to aberrant Hh pathway activity.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-015-1596-z</identifier><identifier>PMID: 26296751</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Animals ; Antineoplastic Agents - pharmacology ; Apoptosis ; Berberine - pharmacology ; Breast cancer ; Cancer ; Care and treatment ; Cell cycle ; Cell Proliferation - drug effects ; Dosage and administration ; Genetic aspects ; Growth ; Hedgehog Proteins - metabolism ; HEK293 Cells ; Humans ; Kinases ; Luciferase ; Medulloblastoma - metabolism ; Medulloblastoma - pathology ; Mice ; Mice, Nude ; Mutation ; Natural products ; NIH 3T3 Cells ; Nonprescription drugs ; Prostaglandins E ; Receptors, G-Protein-Coupled - metabolism ; Signal Transduction - drug effects ; Smoothened Receptor ; Trends</subject><ispartof>BMC cancer, 2015-08, Vol.15 (1), p.595-595, Article 595</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Wang et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c559t-b9b001df279c319cf9ae8d01073c32a9c69b9ae214ecac5187477d4eb2d6c7873</citedby><cites>FETCH-LOGICAL-c559t-b9b001df279c319cf9ae8d01073c32a9c69b9ae214ecac5187477d4eb2d6c7873</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/PMC4546096/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546096/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26296751$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Juan</creatorcontrib><creatorcontrib>Peng, Yuanqiu</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Yang, Jun</creatorcontrib><creatorcontrib>Ding, Ning</creatorcontrib><creatorcontrib>Tan, Wenfu</creatorcontrib><title>Berberine, a natural compound, suppresses Hedgehog signaling pathway activity and cancer growth</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>Berberine (BBR), a natural alkaloid compound, is used as a non-prescription drug in China for treating diarrhea and gastroenteritis. Many studies have revealed that BBR possesses anticancer effect. However, the molecular mechanisms underlying its anticancer action is far from being fully elucidated. This study is aimed to determine the effect of BBR on the hedgehog (Hh) activity and the growth of cancers addiction to Hh activity.
The Hh activity was determined by dual luciferase assays and quantitative RT-PCR analyses. The growth inhibition of BBR on medulloblastoma which was obtained from ptch+/-;p53-/- mice was analyzed by 5-bromo-2-deoxyuridine (Brdu) assays and by allografting the medulloblastoma into nude mice. The data were statistically analyzed by one-way analysis of variance (ANOVA), and multiple comparison between the groups was performed using Dunnett's method.
In this study, we found that BBR significantly inhibited the Hh pathway activity. Meanwhile, we observed that BBR failed to affect the transcriptional factors activities provoked by tumor necrosis factor-α (TNF-α) and Prostaglandin E2 (PGE2), thus suggesting its unique property against Hh pathway activity. Further studies revealed that BBR inhibited the Hh pathway activity by potentially targeting the critical component Smoothened (Smo) and most likely shared the same binding site on Smo with cyclopamine, a classical Smo inhibitor. Finally, we demonstrated that BBR obviously suppressed the Hh-dependent medulloblastoma growth in vitro and in vivo.
Collectively, our study uncovered a novel molecular mechanism responsible for the anticancer action of BBR, thus opening the way for the usage of BBR for therapeutics of cancers addiction to aberrant Hh pathway activity.</description><subject>Analysis</subject><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis</subject><subject>Berberine - pharmacology</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Cell cycle</subject><subject>Cell Proliferation - drug effects</subject><subject>Dosage and administration</subject><subject>Genetic aspects</subject><subject>Growth</subject><subject>Hedgehog Proteins - metabolism</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Kinases</subject><subject>Luciferase</subject><subject>Medulloblastoma - metabolism</subject><subject>Medulloblastoma - pathology</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Mutation</subject><subject>Natural products</subject><subject>NIH 3T3 Cells</subject><subject>Nonprescription drugs</subject><subject>Prostaglandins E</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Signal Transduction - drug effects</subject><subject>Smoothened Receptor</subject><subject>Trends</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkl1r1jAUx4so7kU_gDcSEGTCOpM2aZobYQ51g4Hgy3VI09M2o026JN3cPr15eOZ8KpKLHE5-55-ck3-WvSL4hJC6eh9IUdcsx4TlhIkqv3-S7RPKSV5QzJ_uxHvZQQhXGBNe4_p5tldUhag4I_uZ_Ai-AW8sHCOFrIqLVyPSbprdYttjFJZ59hACBHQObQ-D61EwvVWjsT2aVRxu1R1SOpobE1NgW6SV1eBR791tHF5kzzo1Bnj5sB9mPz9_-nF2nl9-_XJxdnqZa8ZEzBvRpNe1XcGFLonQnVBQt5hgXuqyUEJXokmpglDQSjNSc8p5S6Ep2krzmpeH2Yet7rw0E7QabEyNyNmbSfk76ZSR6xNrBtm7G0kZrbCoksDRg4B31wuEKCcTNIyjsuCWIAnHFeMcM5HQN_-gV27xaSQbqsbpa2hF_lK9GkEa27l0r96IylNGCcWp1zJRJ_-h0mphMtpZ6EzKrwrerQoSE-FX7NUSgrz4_m3Nvt1hB1BjHIIbl2icDWuQbEHtXQgeusfBESw3VpNbq8lkNbmxmrxPNa93J_5Y8cdb5W9j1s3M</recordid><startdate>20150822</startdate><enddate>20150822</enddate><creator>Wang, Juan</creator><creator>Peng, Yuanqiu</creator><creator>Liu, Yuan</creator><creator>Yang, Jun</creator><creator>Ding, Ning</creator><creator>Tan, Wenfu</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150822</creationdate><title>Berberine, a natural compound, suppresses Hedgehog signaling pathway activity and cancer growth</title><author>Wang, Juan ; Peng, Yuanqiu ; Liu, Yuan ; Yang, Jun ; Ding, Ning ; Tan, Wenfu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c559t-b9b001df279c319cf9ae8d01073c32a9c69b9ae214ecac5187477d4eb2d6c7873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Apoptosis</topic><topic>Berberine - pharmacology</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Cell cycle</topic><topic>Cell Proliferation - drug effects</topic><topic>Dosage and administration</topic><topic>Genetic aspects</topic><topic>Growth</topic><topic>Hedgehog Proteins - metabolism</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Kinases</topic><topic>Luciferase</topic><topic>Medulloblastoma - metabolism</topic><topic>Medulloblastoma - pathology</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Mutation</topic><topic>Natural products</topic><topic>NIH 3T3 Cells</topic><topic>Nonprescription drugs</topic><topic>Prostaglandins E</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Signal Transduction - drug effects</topic><topic>Smoothened Receptor</topic><topic>Trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Juan</creatorcontrib><creatorcontrib>Peng, Yuanqiu</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Yang, Jun</creatorcontrib><creatorcontrib>Ding, Ning</creatorcontrib><creatorcontrib>Tan, Wenfu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Juan</au><au>Peng, Yuanqiu</au><au>Liu, Yuan</au><au>Yang, Jun</au><au>Ding, Ning</au><au>Tan, Wenfu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Berberine, a natural compound, suppresses Hedgehog signaling pathway activity and cancer growth</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2015-08-22</date><risdate>2015</risdate><volume>15</volume><issue>1</issue><spage>595</spage><epage>595</epage><pages>595-595</pages><artnum>595</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>Berberine (BBR), a natural alkaloid compound, is used as a non-prescription drug in China for treating diarrhea and gastroenteritis. Many studies have revealed that BBR possesses anticancer effect. However, the molecular mechanisms underlying its anticancer action is far from being fully elucidated. This study is aimed to determine the effect of BBR on the hedgehog (Hh) activity and the growth of cancers addiction to Hh activity.
The Hh activity was determined by dual luciferase assays and quantitative RT-PCR analyses. The growth inhibition of BBR on medulloblastoma which was obtained from ptch+/-;p53-/- mice was analyzed by 5-bromo-2-deoxyuridine (Brdu) assays and by allografting the medulloblastoma into nude mice. The data were statistically analyzed by one-way analysis of variance (ANOVA), and multiple comparison between the groups was performed using Dunnett's method.
In this study, we found that BBR significantly inhibited the Hh pathway activity. Meanwhile, we observed that BBR failed to affect the transcriptional factors activities provoked by tumor necrosis factor-α (TNF-α) and Prostaglandin E2 (PGE2), thus suggesting its unique property against Hh pathway activity. Further studies revealed that BBR inhibited the Hh pathway activity by potentially targeting the critical component Smoothened (Smo) and most likely shared the same binding site on Smo with cyclopamine, a classical Smo inhibitor. Finally, we demonstrated that BBR obviously suppressed the Hh-dependent medulloblastoma growth in vitro and in vivo.
Collectively, our study uncovered a novel molecular mechanism responsible for the anticancer action of BBR, thus opening the way for the usage of BBR for therapeutics of cancers addiction to aberrant Hh pathway activity.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26296751</pmid><doi>10.1186/s12885-015-1596-z</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Antineoplastic Agents - pharmacology Apoptosis Berberine - pharmacology Breast cancer Cancer Care and treatment Cell cycle Cell Proliferation - drug effects Dosage and administration Genetic aspects Growth Hedgehog Proteins - metabolism HEK293 Cells Humans Kinases Luciferase Medulloblastoma - metabolism Medulloblastoma - pathology Mice Mice, Nude Mutation Natural products NIH 3T3 Cells Nonprescription drugs Prostaglandins E Receptors, G-Protein-Coupled - metabolism Signal Transduction - drug effects Smoothened Receptor Trends |
title | Berberine, a natural compound, suppresses Hedgehog signaling pathway activity and cancer growth |
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