SAW PALMETTO BERRY EXTRACT INHIBITS CELL GROWTH AND COX-2 EXPRESSION IN PROSTATIC CANCER CELLS
The cytotoxicity of a commonly used material to alleviate the symptoms of benign prostatic hyperplasia (BPH), Saw Palmetto Berry Extract (SPBE), was examined as neat oil using a set of prostatic cell lines; 267B-1, BRFF-41T and LNCaP. Proliferation of these prostatic derived cell lines is inhibited...
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Veröffentlicht in: | Cell biology international 2001-11, Vol.25 (11), p.1117-1124 |
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description | The cytotoxicity of a commonly used material to alleviate the symptoms of benign prostatic hyperplasia (BPH), Saw Palmetto Berry Extract (SPBE), was examined as neat oil using a set of prostatic cell lines; 267B-1, BRFF-41T and LNCaP. Proliferation of these prostatic derived cell lines is inhibited to different degrees when dosed for 3 days with SPBE. The amount of SPBE required to inhibit 50% growth (IC50) of these cell lines was 20–30nl equivalents of SPBE per ml of medium for cell lines 267B-1 and BRFF-41T and approximately 10-fold more for the LNCaP cell line. The effect of SPBE dosing on these cell lines is not irreversible, since a 30min treatment with SPBE at an IC50concentration does not inhibit their growth. Normal prostate cells were inhibited by 20–25% when grown in the presence of 200nl SPBE equivalent per ml media. Growth of other non-prostatic cancer cell lines, i.e. Jurkat and HT-29, was affected by approx. 50% and 40%, respectively. When LNCaP cells were grown in the presence of dihydrotestosterone and SPBE, the IC50concentration decreased significantly compared to LNCaP cells grown in the presence of serum and SPBE. Reduced cellular growth after SPBE treatment of these cell lines may relate to decreased expression of Cox-2 and may be due to changes observed in the expression of Bcl-2. Expression of Cox-1 under similar conditions is not affected because of its constitutive expression. Since increased Cox-2 expression is associated with an increased incidence of prostate cancer, and decrease in its expression by SPBE would provide a basis for further investigation of its use against BPH and in prostatic cancer chemoprevention. |
doi_str_mv | 10.1006/cbir.2001.0779 |
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Proliferation of these prostatic derived cell lines is inhibited to different degrees when dosed for 3 days with SPBE. The amount of SPBE required to inhibit 50% growth (IC50) of these cell lines was 20–30nl equivalents of SPBE per ml of medium for cell lines 267B-1 and BRFF-41T and approximately 10-fold more for the LNCaP cell line. The effect of SPBE dosing on these cell lines is not irreversible, since a 30min treatment with SPBE at an IC50concentration does not inhibit their growth. Normal prostate cells were inhibited by 20–25% when grown in the presence of 200nl SPBE equivalent per ml media. Growth of other non-prostatic cancer cell lines, i.e. Jurkat and HT-29, was affected by approx. 50% and 40%, respectively. When LNCaP cells were grown in the presence of dihydrotestosterone and SPBE, the IC50concentration decreased significantly compared to LNCaP cells grown in the presence of serum and SPBE. Reduced cellular growth after SPBE treatment of these cell lines may relate to decreased expression of Cox-2 and may be due to changes observed in the expression of Bcl-2. Expression of Cox-1 under similar conditions is not affected because of its constitutive expression. Since increased Cox-2 expression is associated with an increased incidence of prostate cancer, and decrease in its expression by SPBE would provide a basis for further investigation of its use against BPH and in prostatic cancer chemoprevention.</description><identifier>ISSN: 1065-6995</identifier><identifier>EISSN: 1095-8355</identifier><identifier>DOI: 10.1006/cbir.2001.0779</identifier><identifier>PMID: 11913955</identifier><language>eng</language><publisher>Oxford, UK: Elsevier Ltd</publisher><subject>Androgen Antagonists - pharmacology ; Bcl-2 ; cell growth inhibition ; Cox-1 ; Cox-2 ; Cyclooxygenase 2 ; Dose-Response Relationship, Drug ; Gene Expression Regulation, Neoplastic - drug effects ; Genes, bcl-2 - physiology ; Growth Inhibitors - pharmacology ; Humans ; Isoenzymes - biosynthesis ; Isoenzymes - genetics ; Male ; Membrane Proteins ; MTT and SRB assays ; Plant Extracts - pharmacology ; Prostaglandin-Endoperoxide Synthases - biosynthesis ; Prostaglandin-Endoperoxide Synthases - genetics ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; Saw Palmetto berry extract ; Serenoa ; Tumor Cells, Cultured</subject><ispartof>Cell biology international, 2001-11, Vol.25 (11), p.1117-1124</ispartof><rights>2001 Academic Press</rights><rights>The Author(s) Journal compilation © 2001 International Federation for Cell Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5293-35e987dc927bc7a3542b7f60170ec6d9445dc7b6ceb5bc66423e9c106940e7133</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1006%2Fcbir.2001.0779$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1006%2Fcbir.2001.0779$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11913955$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goldmann, Wolfgang H.</creatorcontrib><creatorcontrib>Sharma, Amita L.</creatorcontrib><creatorcontrib>Currier, Steve J.</creatorcontrib><creatorcontrib>Johnston, Paul D.</creatorcontrib><creatorcontrib>Rana, Ajay</creatorcontrib><creatorcontrib>Pal Sharma, C.</creatorcontrib><title>SAW PALMETTO BERRY EXTRACT INHIBITS CELL GROWTH AND COX-2 EXPRESSION IN PROSTATIC CANCER CELLS</title><title>Cell biology international</title><addtitle>Cell Biol Int</addtitle><description>The cytotoxicity of a commonly used material to alleviate the symptoms of benign prostatic hyperplasia (BPH), Saw Palmetto Berry Extract (SPBE), was examined as neat oil using a set of prostatic cell lines; 267B-1, BRFF-41T and LNCaP. Proliferation of these prostatic derived cell lines is inhibited to different degrees when dosed for 3 days with SPBE. The amount of SPBE required to inhibit 50% growth (IC50) of these cell lines was 20–30nl equivalents of SPBE per ml of medium for cell lines 267B-1 and BRFF-41T and approximately 10-fold more for the LNCaP cell line. The effect of SPBE dosing on these cell lines is not irreversible, since a 30min treatment with SPBE at an IC50concentration does not inhibit their growth. Normal prostate cells were inhibited by 20–25% when grown in the presence of 200nl SPBE equivalent per ml media. Growth of other non-prostatic cancer cell lines, i.e. Jurkat and HT-29, was affected by approx. 50% and 40%, respectively. When LNCaP cells were grown in the presence of dihydrotestosterone and SPBE, the IC50concentration decreased significantly compared to LNCaP cells grown in the presence of serum and SPBE. Reduced cellular growth after SPBE treatment of these cell lines may relate to decreased expression of Cox-2 and may be due to changes observed in the expression of Bcl-2. Expression of Cox-1 under similar conditions is not affected because of its constitutive expression. Since increased Cox-2 expression is associated with an increased incidence of prostate cancer, and decrease in its expression by SPBE would provide a basis for further investigation of its use against BPH and in prostatic cancer chemoprevention.</description><subject>Androgen Antagonists - pharmacology</subject><subject>Bcl-2</subject><subject>cell growth inhibition</subject><subject>Cox-1</subject><subject>Cox-2</subject><subject>Cyclooxygenase 2</subject><subject>Dose-Response Relationship, Drug</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Genes, bcl-2 - physiology</subject><subject>Growth Inhibitors - pharmacology</subject><subject>Humans</subject><subject>Isoenzymes - biosynthesis</subject><subject>Isoenzymes - genetics</subject><subject>Male</subject><subject>Membrane Proteins</subject><subject>MTT and SRB assays</subject><subject>Plant Extracts - pharmacology</subject><subject>Prostaglandin-Endoperoxide Synthases - biosynthesis</subject><subject>Prostaglandin-Endoperoxide Synthases - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Saw Palmetto berry extract</subject><subject>Serenoa</subject><subject>Tumor Cells, Cultured</subject><issn>1065-6995</issn><issn>1095-8355</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE2P0zAQhiMEYpeFK0fkE7cUf8R2fUyzaRspJFUS6HLBSpypFGi3i90C--9xSAUnxGnm8LyvZp4geE3wjGAs3plusDOKMZlhKdWT4JpgxcM54_zpuAseCqX4VfDCuS-eItFcPA-uCFGEKc6vg891vEWbOH-fNk2JFmlVfULpXVPFSYOyYp0tsqZGSZrnaFWV22aN4uIWJeVdSD22qdK6zsrCk2hTlXUTN1mCkrhI0up3qH4ZPNu1ewevLvMm-LBMm2Qd5uUqS-I8NJwqFjIOai57o6jsjGwZj2gndwITicGIXkUR743shIGOd0aIiDJQxr-nIgySMHYTvJ16H-zx2xncSR8GZ2C_b-_heHbaM5RGhHpwNoHGHp2zsNMPdji09lETrEejejSqR6N6NOoDby7N5-4A_V_8otAD0QT8GPbw-J86nSyygmA-XhxOscGd4OefWGu_aiGZ5HpbrPTHTb1aULXUS8_PJx68xu8DWO3MAPcG-sGCOen-OPzrhV-3UJq-</recordid><startdate>200111</startdate><enddate>200111</enddate><creator>Goldmann, Wolfgang H.</creator><creator>Sharma, Amita L.</creator><creator>Currier, Steve J.</creator><creator>Johnston, Paul D.</creator><creator>Rana, Ajay</creator><creator>Pal Sharma, C.</creator><general>Elsevier Ltd</general><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>200111</creationdate><title>SAW PALMETTO BERRY EXTRACT INHIBITS CELL GROWTH AND COX-2 EXPRESSION IN PROSTATIC CANCER CELLS</title><author>Goldmann, Wolfgang H. ; Sharma, Amita L. ; Currier, Steve J. ; Johnston, Paul D. ; Rana, Ajay ; Pal Sharma, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5293-35e987dc927bc7a3542b7f60170ec6d9445dc7b6ceb5bc66423e9c106940e7133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Androgen Antagonists - pharmacology</topic><topic>Bcl-2</topic><topic>cell growth inhibition</topic><topic>Cox-1</topic><topic>Cox-2</topic><topic>Cyclooxygenase 2</topic><topic>Dose-Response Relationship, Drug</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Genes, bcl-2 - physiology</topic><topic>Growth Inhibitors - pharmacology</topic><topic>Humans</topic><topic>Isoenzymes - biosynthesis</topic><topic>Isoenzymes - genetics</topic><topic>Male</topic><topic>Membrane Proteins</topic><topic>MTT and SRB assays</topic><topic>Plant Extracts - pharmacology</topic><topic>Prostaglandin-Endoperoxide Synthases - biosynthesis</topic><topic>Prostaglandin-Endoperoxide Synthases - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Saw Palmetto berry extract</topic><topic>Serenoa</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goldmann, Wolfgang H.</creatorcontrib><creatorcontrib>Sharma, Amita L.</creatorcontrib><creatorcontrib>Currier, Steve J.</creatorcontrib><creatorcontrib>Johnston, Paul D.</creatorcontrib><creatorcontrib>Rana, Ajay</creatorcontrib><creatorcontrib>Pal Sharma, C.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cell biology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goldmann, Wolfgang H.</au><au>Sharma, Amita L.</au><au>Currier, Steve J.</au><au>Johnston, Paul D.</au><au>Rana, Ajay</au><au>Pal Sharma, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SAW PALMETTO BERRY EXTRACT INHIBITS CELL GROWTH AND COX-2 EXPRESSION IN PROSTATIC CANCER CELLS</atitle><jtitle>Cell biology international</jtitle><addtitle>Cell Biol Int</addtitle><date>2001-11</date><risdate>2001</risdate><volume>25</volume><issue>11</issue><spage>1117</spage><epage>1124</epage><pages>1117-1124</pages><issn>1065-6995</issn><eissn>1095-8355</eissn><abstract>The cytotoxicity of a commonly used material to alleviate the symptoms of benign prostatic hyperplasia (BPH), Saw Palmetto Berry Extract (SPBE), was examined as neat oil using a set of prostatic cell lines; 267B-1, BRFF-41T and LNCaP. Proliferation of these prostatic derived cell lines is inhibited to different degrees when dosed for 3 days with SPBE. The amount of SPBE required to inhibit 50% growth (IC50) of these cell lines was 20–30nl equivalents of SPBE per ml of medium for cell lines 267B-1 and BRFF-41T and approximately 10-fold more for the LNCaP cell line. The effect of SPBE dosing on these cell lines is not irreversible, since a 30min treatment with SPBE at an IC50concentration does not inhibit their growth. Normal prostate cells were inhibited by 20–25% when grown in the presence of 200nl SPBE equivalent per ml media. Growth of other non-prostatic cancer cell lines, i.e. Jurkat and HT-29, was affected by approx. 50% and 40%, respectively. When LNCaP cells were grown in the presence of dihydrotestosterone and SPBE, the IC50concentration decreased significantly compared to LNCaP cells grown in the presence of serum and SPBE. Reduced cellular growth after SPBE treatment of these cell lines may relate to decreased expression of Cox-2 and may be due to changes observed in the expression of Bcl-2. Expression of Cox-1 under similar conditions is not affected because of its constitutive expression. Since increased Cox-2 expression is associated with an increased incidence of prostate cancer, and decrease in its expression by SPBE would provide a basis for further investigation of its use against BPH and in prostatic cancer chemoprevention.</abstract><cop>Oxford, UK</cop><pub>Elsevier Ltd</pub><pmid>11913955</pmid><doi>10.1006/cbir.2001.0779</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Androgen Antagonists - pharmacology Bcl-2 cell growth inhibition Cox-1 Cox-2 Cyclooxygenase 2 Dose-Response Relationship, Drug Gene Expression Regulation, Neoplastic - drug effects Genes, bcl-2 - physiology Growth Inhibitors - pharmacology Humans Isoenzymes - biosynthesis Isoenzymes - genetics Male Membrane Proteins MTT and SRB assays Plant Extracts - pharmacology Prostaglandin-Endoperoxide Synthases - biosynthesis Prostaglandin-Endoperoxide Synthases - genetics Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology Saw Palmetto berry extract Serenoa Tumor Cells, Cultured |
title | SAW PALMETTO BERRY EXTRACT INHIBITS CELL GROWTH AND COX-2 EXPRESSION IN PROSTATIC CANCER CELLS |
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