Inositol Hexaphosphate (IP6) Inhibits Cellular Proliferation In Melanoma
Inositol Hexaphosphate (IP6) is a naturally occurring polyphosphorylated carbohydrate found in food sources high in fiber content. We have previously reported IP6 to have significant inhibitory effects against pancreatic cancer in vitro. We hypothesized that the IP6 would significantly inhibit cell...
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description | Inositol Hexaphosphate (IP6) is a naturally occurring polyphosphorylated carbohydrate found in food sources high in fiber content. We have previously reported IP6 to have significant inhibitory effects against pancreatic cancer
in vitro. We hypothesized that the IP6 would significantly inhibit cell growth of cutaneous melanoma
in vitro.
The melanoma line HTB68 was cultured using standard techniques and treated with IP6 at doses ranging from 0.2 to 1.0 m
m/well. Cell viability was measured by MTT at 72 h. VEGF production was measured in the cell supernatants by ELISA. Apoptosis was evaluated by Annexin V-FITC and results calculated using FACS analysis. Statistical analysis was performed by ANOVA.
Significant reductions (
P < 0.001) in cellular proliferation were observed with IP6. Overall, IP6 exhibited a mean inhibition of cell growth of 52.1 ± 11.5% (range, 1.6–83.0%) at 72 h of incubation. VEGF production was significantly reduced (
P < 0.001) by the addition of IP6 (7.5 pg/ml) compared to control (40.9 pg/ml). IP6 significantly increased (
P = 0.029) late apoptosis from 5.3 to 7.0% gated events. No changes in necrosis or early apoptosis were observed.
Adjuvant treatment of melanoma continues to challenge clinicians and patients. Our findings that IP6 significantly decreased cellular growth, VEGF production and increased late apoptosis in melanoma suggest its potential therapeutic value. Further
in vivo studies are planned to evaluate safety and clinical utility of this agent. |
doi_str_mv | 10.1016/j.jss.2006.02.023 |
format | Article |
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in vitro. We hypothesized that the IP6 would significantly inhibit cell growth of cutaneous melanoma
in vitro.
The melanoma line HTB68 was cultured using standard techniques and treated with IP6 at doses ranging from 0.2 to 1.0 m
m/well. Cell viability was measured by MTT at 72 h. VEGF production was measured in the cell supernatants by ELISA. Apoptosis was evaluated by Annexin V-FITC and results calculated using FACS analysis. Statistical analysis was performed by ANOVA.
Significant reductions (
P < 0.001) in cellular proliferation were observed with IP6. Overall, IP6 exhibited a mean inhibition of cell growth of 52.1 ± 11.5% (range, 1.6–83.0%) at 72 h of incubation. VEGF production was significantly reduced (
P < 0.001) by the addition of IP6 (7.5 pg/ml) compared to control (40.9 pg/ml). IP6 significantly increased (
P = 0.029) late apoptosis from 5.3 to 7.0% gated events. No changes in necrosis or early apoptosis were observed.
Adjuvant treatment of melanoma continues to challenge clinicians and patients. Our findings that IP6 significantly decreased cellular growth, VEGF production and increased late apoptosis in melanoma suggest its potential therapeutic value. Further
in vivo studies are planned to evaluate safety and clinical utility of this agent.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2006.02.023</identifier><identifier>PMID: 16563438</identifier><identifier>CODEN: JSGRA2</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>apoptosis ; Apoptosis - drug effects ; Biological and medical sciences ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Dermatology ; General aspects ; Humans ; inositol hexaphosphate ; Medical sciences ; melanoma ; Melanoma - drug therapy ; Melanoma - metabolism ; Melanoma - pathology ; Phytic Acid - pharmacology ; Phytic Acid - therapeutic use ; Tumors of the skin and soft tissue. Premalignant lesions ; Vascular Endothelial Growth Factor A - metabolism ; VEGF</subject><ispartof>The Journal of surgical research, 2006-06, Vol.133 (1), p.3-6</ispartof><rights>2006 Elsevier Inc.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-253dc5447cbc63ad3d35640c85c0637c84b3e740845bac7e88a22b36fe22fe523</citedby><cites>FETCH-LOGICAL-c381t-253dc5447cbc63ad3d35640c85c0637c84b3e740845bac7e88a22b36fe22fe523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022480406000710$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,23911,23912,25120,27903,27904,65308</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17884680$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16563438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rizvi, Irfan</creatorcontrib><creatorcontrib>Riggs, Dale R.</creatorcontrib><creatorcontrib>Jackson, Barbara J.</creatorcontrib><creatorcontrib>Ng, Alex</creatorcontrib><creatorcontrib>Cunningham, Cynthia</creatorcontrib><creatorcontrib>Mcfadden, David W.</creatorcontrib><title>Inositol Hexaphosphate (IP6) Inhibits Cellular Proliferation In Melanoma</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Inositol Hexaphosphate (IP6) is a naturally occurring polyphosphorylated carbohydrate found in food sources high in fiber content. We have previously reported IP6 to have significant inhibitory effects against pancreatic cancer
in vitro. We hypothesized that the IP6 would significantly inhibit cell growth of cutaneous melanoma
in vitro.
The melanoma line HTB68 was cultured using standard techniques and treated with IP6 at doses ranging from 0.2 to 1.0 m
m/well. Cell viability was measured by MTT at 72 h. VEGF production was measured in the cell supernatants by ELISA. Apoptosis was evaluated by Annexin V-FITC and results calculated using FACS analysis. Statistical analysis was performed by ANOVA.
Significant reductions (
P < 0.001) in cellular proliferation were observed with IP6. Overall, IP6 exhibited a mean inhibition of cell growth of 52.1 ± 11.5% (range, 1.6–83.0%) at 72 h of incubation. VEGF production was significantly reduced (
P < 0.001) by the addition of IP6 (7.5 pg/ml) compared to control (40.9 pg/ml). IP6 significantly increased (
P = 0.029) late apoptosis from 5.3 to 7.0% gated events. No changes in necrosis or early apoptosis were observed.
Adjuvant treatment of melanoma continues to challenge clinicians and patients. Our findings that IP6 significantly decreased cellular growth, VEGF production and increased late apoptosis in melanoma suggest its potential therapeutic value. Further
in vivo studies are planned to evaluate safety and clinical utility of this agent.</description><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Biological and medical sciences</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Dermatology</subject><subject>General aspects</subject><subject>Humans</subject><subject>inositol hexaphosphate</subject><subject>Medical sciences</subject><subject>melanoma</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>Phytic Acid - pharmacology</subject><subject>Phytic Acid - therapeutic use</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>VEGF</subject><issn>0022-4804</issn><issn>1095-8673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMotn78AC-yF0UPW7P5Lp6kqC1U7EHPIZudpSnbTU12Rf-9KS30JgwMwzwzvDwIXRV4VOBCPKxGqxhHBGMxwiQVPULDAo95roSkx2iIMSE5U5gN0FmMK5zmsaSnaFAILiijaoims9ZH1_kmm8KP2Sx93CxNB9ndbCHus1m7dKXrYjaBpukbE7JF8I2rIZjO-TbtszdoTOvX5gKd1KaJcLnv5-jz5fljMs3n76-zydM8t1QVXU44rSxnTNrSCmoqWlEuGLaKWyyotIqVFCTDivHSWAlKGUJKKmogpAZO6Dm63f3dBP_VQ-z02kWb4pkWfB-1kGMuGZcJLHagDT7GALXeBLc24VcXWG_16ZVO-vRWn8YkFU031_vnfbmG6nCx95WAmz1gojVNHUxrXTxwUikmFE7c446DpOLbQdDROmgtVC6A7XTl3T8x_gDwiowP</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>Rizvi, Irfan</creator><creator>Riggs, Dale R.</creator><creator>Jackson, Barbara J.</creator><creator>Ng, Alex</creator><creator>Cunningham, Cynthia</creator><creator>Mcfadden, David W.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>20060601</creationdate><title>Inositol Hexaphosphate (IP6) Inhibits Cellular Proliferation In Melanoma</title><author>Rizvi, Irfan ; Riggs, Dale R. ; Jackson, Barbara J. ; Ng, Alex ; Cunningham, Cynthia ; Mcfadden, David W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-253dc5447cbc63ad3d35640c85c0637c84b3e740845bac7e88a22b36fe22fe523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biological and medical sciences</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Dermatology</topic><topic>General aspects</topic><topic>Humans</topic><topic>inositol hexaphosphate</topic><topic>Medical sciences</topic><topic>melanoma</topic><topic>Melanoma - drug therapy</topic><topic>Melanoma - metabolism</topic><topic>Melanoma - pathology</topic><topic>Phytic Acid - pharmacology</topic><topic>Phytic Acid - therapeutic use</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>VEGF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rizvi, Irfan</creatorcontrib><creatorcontrib>Riggs, Dale R.</creatorcontrib><creatorcontrib>Jackson, Barbara J.</creatorcontrib><creatorcontrib>Ng, Alex</creatorcontrib><creatorcontrib>Cunningham, Cynthia</creatorcontrib><creatorcontrib>Mcfadden, David W.</creatorcontrib><collection>Pascal-Francis</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>The Journal of surgical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rizvi, Irfan</au><au>Riggs, Dale R.</au><au>Jackson, Barbara J.</au><au>Ng, Alex</au><au>Cunningham, Cynthia</au><au>Mcfadden, David W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inositol Hexaphosphate (IP6) Inhibits Cellular Proliferation In Melanoma</atitle><jtitle>The Journal of surgical research</jtitle><addtitle>J Surg Res</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>133</volume><issue>1</issue><spage>3</spage><epage>6</epage><pages>3-6</pages><issn>0022-4804</issn><eissn>1095-8673</eissn><coden>JSGRA2</coden><abstract>Inositol Hexaphosphate (IP6) is a naturally occurring polyphosphorylated carbohydrate found in food sources high in fiber content. We have previously reported IP6 to have significant inhibitory effects against pancreatic cancer
in vitro. We hypothesized that the IP6 would significantly inhibit cell growth of cutaneous melanoma
in vitro.
The melanoma line HTB68 was cultured using standard techniques and treated with IP6 at doses ranging from 0.2 to 1.0 m
m/well. Cell viability was measured by MTT at 72 h. VEGF production was measured in the cell supernatants by ELISA. Apoptosis was evaluated by Annexin V-FITC and results calculated using FACS analysis. Statistical analysis was performed by ANOVA.
Significant reductions (
P < 0.001) in cellular proliferation were observed with IP6. Overall, IP6 exhibited a mean inhibition of cell growth of 52.1 ± 11.5% (range, 1.6–83.0%) at 72 h of incubation. VEGF production was significantly reduced (
P < 0.001) by the addition of IP6 (7.5 pg/ml) compared to control (40.9 pg/ml). IP6 significantly increased (
P = 0.029) late apoptosis from 5.3 to 7.0% gated events. No changes in necrosis or early apoptosis were observed.
Adjuvant treatment of melanoma continues to challenge clinicians and patients. Our findings that IP6 significantly decreased cellular growth, VEGF production and increased late apoptosis in melanoma suggest its potential therapeutic value. Further
in vivo studies are planned to evaluate safety and clinical utility of this agent.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>16563438</pmid><doi>10.1016/j.jss.2006.02.023</doi><tpages>4</tpages></addata></record> |
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subjects | apoptosis Apoptosis - drug effects Biological and medical sciences Cell Line, Tumor Cell Proliferation - drug effects Dermatology General aspects Humans inositol hexaphosphate Medical sciences melanoma Melanoma - drug therapy Melanoma - metabolism Melanoma - pathology Phytic Acid - pharmacology Phytic Acid - therapeutic use Tumors of the skin and soft tissue. Premalignant lesions Vascular Endothelial Growth Factor A - metabolism VEGF |
title | Inositol Hexaphosphate (IP6) Inhibits Cellular Proliferation In Melanoma |
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