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Combination of Lipitor and Celebrex inhibits prostate cancer VCaP cells in vitro and in vivo
Lipitor is a cholesterol-lowering drug and Celebrex is a Cyclooxygenase-2 inhibitor. We investigated the effects of Lipitor and Celebrex on human prostate cancer VCaP cells cultured in vitro and grown as orthotopic xenograft tumors in SCID mice. Apoptosis was measured by morphological assessment and...
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Published in: | Anticancer research 2014-07, Vol.34 (7), p.3357-3363 |
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creator | Huang, Huarong Cui, Xiao-Xing Chen, Shaohua Goodin, Susan Liu, Yue He, Yan Li, Dongli Wang, Hong Van Doren, Jeremiah Dipaola, Robert S Conney, Allan H Zheng, Xi |
description | Lipitor is a cholesterol-lowering drug and Celebrex is a Cyclooxygenase-2 inhibitor. We investigated the effects of Lipitor and Celebrex on human prostate cancer VCaP cells cultured in vitro and grown as orthotopic xenograft tumors in SCID mice.
Apoptosis was measured by morphological assessment and caspase-3 assay. Nuclear factor-kappa B (NF-κB) activation was determined by luciferase reporter assay. B-cell lymphoma-2 (Bcl2) was measured by western blotting and immunohistochemistry. Orthotopic prostate tumors were monitored by the IVIS imaging system.
the combination of Lipitor and Celebrex had stronger effects on the growth and apoptosis of VCaP cells than did either drug alone. The combination more potently inhibited activation of NFκB and expression of Bcl2 than either drug alone. The growth of orthotopic VCaP prostate tumors was strongly inhibited by treatment with the drug combination.
Administration of Lipitor and Celebrex in combination may be an effective strategy for inhibiting the growth of prostate cancer. |
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Apoptosis was measured by morphological assessment and caspase-3 assay. Nuclear factor-kappa B (NF-κB) activation was determined by luciferase reporter assay. B-cell lymphoma-2 (Bcl2) was measured by western blotting and immunohistochemistry. Orthotopic prostate tumors were monitored by the IVIS imaging system.
the combination of Lipitor and Celebrex had stronger effects on the growth and apoptosis of VCaP cells than did either drug alone. The combination more potently inhibited activation of NFκB and expression of Bcl2 than either drug alone. The growth of orthotopic VCaP prostate tumors was strongly inhibited by treatment with the drug combination.
Administration of Lipitor and Celebrex in combination may be an effective strategy for inhibiting the growth of prostate cancer.</description><identifier>ISSN: 0250-7005</identifier><identifier>EISSN: 1791-7530</identifier><identifier>PMID: 24982340</identifier><language>eng</language><publisher>Greece</publisher><subject><![CDATA[Animals ; Anticholesteremic Agents - administration & dosage ; Anticholesteremic Agents - pharmacology ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Apoptosis - drug effects ; Atorvastatin Calcium ; Celecoxib ; Cell Growth Processes - drug effects ; Cell Line, Tumor ; Cyclooxygenase 2 Inhibitors - administration & dosage ; Cyclooxygenase 2 Inhibitors - pharmacology ; Heptanoic Acids - administration & dosage ; Heptanoic Acids - pharmacology ; Humans ; Male ; Mice ; Mice, SCID ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - pathology ; Pyrazoles - administration & dosage ; Pyrazoles - pharmacology ; Pyrroles - administration & dosage ; Pyrroles - pharmacology ; Sulfonamides - administration & dosage ; Sulfonamides - pharmacology ; Xenograft Model Antitumor Assays]]></subject><ispartof>Anticancer research, 2014-07, Vol.34 (7), p.3357-3363</ispartof><rights>Copyright© 2014 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24982340$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Huarong</creatorcontrib><creatorcontrib>Cui, Xiao-Xing</creatorcontrib><creatorcontrib>Chen, Shaohua</creatorcontrib><creatorcontrib>Goodin, Susan</creatorcontrib><creatorcontrib>Liu, Yue</creatorcontrib><creatorcontrib>He, Yan</creatorcontrib><creatorcontrib>Li, Dongli</creatorcontrib><creatorcontrib>Wang, Hong</creatorcontrib><creatorcontrib>Van Doren, Jeremiah</creatorcontrib><creatorcontrib>Dipaola, Robert S</creatorcontrib><creatorcontrib>Conney, Allan H</creatorcontrib><creatorcontrib>Zheng, Xi</creatorcontrib><title>Combination of Lipitor and Celebrex inhibits prostate cancer VCaP cells in vitro and in vivo</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>Lipitor is a cholesterol-lowering drug and Celebrex is a Cyclooxygenase-2 inhibitor. We investigated the effects of Lipitor and Celebrex on human prostate cancer VCaP cells cultured in vitro and grown as orthotopic xenograft tumors in SCID mice.
Apoptosis was measured by morphological assessment and caspase-3 assay. Nuclear factor-kappa B (NF-κB) activation was determined by luciferase reporter assay. B-cell lymphoma-2 (Bcl2) was measured by western blotting and immunohistochemistry. Orthotopic prostate tumors were monitored by the IVIS imaging system.
the combination of Lipitor and Celebrex had stronger effects on the growth and apoptosis of VCaP cells than did either drug alone. The combination more potently inhibited activation of NFκB and expression of Bcl2 than either drug alone. The growth of orthotopic VCaP prostate tumors was strongly inhibited by treatment with the drug combination.
Administration of Lipitor and Celebrex in combination may be an effective strategy for inhibiting the growth of prostate cancer.</description><subject>Animals</subject><subject>Anticholesteremic Agents - administration & dosage</subject><subject>Anticholesteremic Agents - pharmacology</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Apoptosis - drug effects</subject><subject>Atorvastatin Calcium</subject><subject>Celecoxib</subject><subject>Cell Growth Processes - drug effects</subject><subject>Cell Line, Tumor</subject><subject>Cyclooxygenase 2 Inhibitors - administration & dosage</subject><subject>Cyclooxygenase 2 Inhibitors - pharmacology</subject><subject>Heptanoic Acids - administration & dosage</subject><subject>Heptanoic Acids - pharmacology</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Pyrazoles - administration & dosage</subject><subject>Pyrazoles - pharmacology</subject><subject>Pyrroles - administration & dosage</subject><subject>Pyrroles - pharmacology</subject><subject>Sulfonamides - administration & dosage</subject><subject>Sulfonamides - pharmacology</subject><subject>Xenograft Model Antitumor Assays</subject><issn>0250-7005</issn><issn>1791-7530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpVUE1LxDAUDKK46-pfkBy9FJK0SduLIMUvWNCDehJCmr64kTapSXbRf29dV9HTMLx5M8zsoTkta5qVPCf7aE4YJ1lJCJ-hoxhfCRGirvJDNGNFXbG8IHP03PihtU4l6x32Bi_taJMPWLkON9BDG-AdW7eyrU0Rj8HHpBJgrZyGgJ8adY819H2cNHhjU_Dbzy3Z-GN0YFQf4WSHC_R4dfnQ3GTLu-vb5mKZjUyIlPFKEEV4WZcTaKq1oZQLXRjg3LQcdFFQRXXdlV1rtDKmpUCogIqJiXc6X6Dzb99x3Q7QaXApqF6OwQ4qfEivrPx_cXYlX_xG8mkIxvPJ4GxnEPzbGmKSg41fvZQDv46S8oKxui65mKSnf7N-Q34mzT8Bps52JQ</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Huang, Huarong</creator><creator>Cui, Xiao-Xing</creator><creator>Chen, Shaohua</creator><creator>Goodin, Susan</creator><creator>Liu, Yue</creator><creator>He, Yan</creator><creator>Li, Dongli</creator><creator>Wang, Hong</creator><creator>Van Doren, Jeremiah</creator><creator>Dipaola, Robert S</creator><creator>Conney, Allan H</creator><creator>Zheng, Xi</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201407</creationdate><title>Combination of Lipitor and Celebrex inhibits prostate cancer VCaP cells in vitro and in vivo</title><author>Huang, Huarong ; Cui, Xiao-Xing ; Chen, Shaohua ; Goodin, Susan ; Liu, Yue ; He, Yan ; Li, Dongli ; Wang, Hong ; Van Doren, Jeremiah ; Dipaola, Robert S ; Conney, Allan H ; Zheng, Xi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-5860a057970a0c1ccf1156c4fe55fb5ec441a1c9d7dbfcaffb1e016e826bfcdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Anticholesteremic Agents - administration & dosage</topic><topic>Anticholesteremic Agents - pharmacology</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Apoptosis - drug effects</topic><topic>Atorvastatin Calcium</topic><topic>Celecoxib</topic><topic>Cell Growth Processes - drug effects</topic><topic>Cell Line, Tumor</topic><topic>Cyclooxygenase 2 Inhibitors - administration & dosage</topic><topic>Cyclooxygenase 2 Inhibitors - pharmacology</topic><topic>Heptanoic Acids - administration & dosage</topic><topic>Heptanoic Acids - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, SCID</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Pyrazoles - administration & dosage</topic><topic>Pyrazoles - pharmacology</topic><topic>Pyrroles - administration & dosage</topic><topic>Pyrroles - pharmacology</topic><topic>Sulfonamides - administration & dosage</topic><topic>Sulfonamides - pharmacology</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Huarong</creatorcontrib><creatorcontrib>Cui, Xiao-Xing</creatorcontrib><creatorcontrib>Chen, Shaohua</creatorcontrib><creatorcontrib>Goodin, Susan</creatorcontrib><creatorcontrib>Liu, Yue</creatorcontrib><creatorcontrib>He, Yan</creatorcontrib><creatorcontrib>Li, Dongli</creatorcontrib><creatorcontrib>Wang, Hong</creatorcontrib><creatorcontrib>Van Doren, Jeremiah</creatorcontrib><creatorcontrib>Dipaola, Robert S</creatorcontrib><creatorcontrib>Conney, Allan H</creatorcontrib><creatorcontrib>Zheng, Xi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Huarong</au><au>Cui, Xiao-Xing</au><au>Chen, Shaohua</au><au>Goodin, Susan</au><au>Liu, Yue</au><au>He, Yan</au><au>Li, Dongli</au><au>Wang, Hong</au><au>Van Doren, Jeremiah</au><au>Dipaola, Robert S</au><au>Conney, Allan H</au><au>Zheng, Xi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combination of Lipitor and Celebrex inhibits prostate cancer VCaP cells in vitro and in vivo</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2014-07</date><risdate>2014</risdate><volume>34</volume><issue>7</issue><spage>3357</spage><epage>3363</epage><pages>3357-3363</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>Lipitor is a cholesterol-lowering drug and Celebrex is a Cyclooxygenase-2 inhibitor. We investigated the effects of Lipitor and Celebrex on human prostate cancer VCaP cells cultured in vitro and grown as orthotopic xenograft tumors in SCID mice.
Apoptosis was measured by morphological assessment and caspase-3 assay. Nuclear factor-kappa B (NF-κB) activation was determined by luciferase reporter assay. B-cell lymphoma-2 (Bcl2) was measured by western blotting and immunohistochemistry. Orthotopic prostate tumors were monitored by the IVIS imaging system.
the combination of Lipitor and Celebrex had stronger effects on the growth and apoptosis of VCaP cells than did either drug alone. The combination more potently inhibited activation of NFκB and expression of Bcl2 than either drug alone. The growth of orthotopic VCaP prostate tumors was strongly inhibited by treatment with the drug combination.
Administration of Lipitor and Celebrex in combination may be an effective strategy for inhibiting the growth of prostate cancer.</abstract><cop>Greece</cop><pmid>24982340</pmid><tpages>7</tpages></addata></record> |
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subjects | Animals Anticholesteremic Agents - administration & dosage Anticholesteremic Agents - pharmacology Antineoplastic Combined Chemotherapy Protocols - pharmacology Apoptosis - drug effects Atorvastatin Calcium Celecoxib Cell Growth Processes - drug effects Cell Line, Tumor Cyclooxygenase 2 Inhibitors - administration & dosage Cyclooxygenase 2 Inhibitors - pharmacology Heptanoic Acids - administration & dosage Heptanoic Acids - pharmacology Humans Male Mice Mice, SCID Prostatic Neoplasms - drug therapy Prostatic Neoplasms - pathology Pyrazoles - administration & dosage Pyrazoles - pharmacology Pyrroles - administration & dosage Pyrroles - pharmacology Sulfonamides - administration & dosage Sulfonamides - pharmacology Xenograft Model Antitumor Assays |
title | Combination of Lipitor and Celebrex inhibits prostate cancer VCaP cells in vitro and in vivo |
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