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Detection of Alkaline Sphingomyelinase Activity in Human Stool: Proposed Role as a New Diagnostic and Prognostic Marker of Colorectal Cancer
Objectives: Intestinal alkaline sphingomyelinase, by exerting a major role in dietary sphingomyelin digestion, is responsible for the generation of messengers able to trigger the rapid turnover and apoptosis in intestinal epithelial cells. Markedly reduced mucosal alkaline sphingomyelinase activity...
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Published in: | Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2005-04, Vol.14 (4), p.856-862 |
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creator | DI MARZIO, Luisa DI LEO, Alfredo CIFONE, Maria Grazia CINQUE, Benedetta FANINI, Donatella AGNIFILI, Alessio BERLOCO, Pasquale LINSALATA, Michele LORUSSO, Dionigi BARONE, Michele DE SIMONE, Claudio |
description | Objectives: Intestinal alkaline sphingomyelinase, by exerting a major role in dietary sphingomyelin digestion, is responsible
for the generation of messengers able to trigger the rapid turnover and apoptosis in intestinal epithelial cells. Markedly
reduced mucosal alkaline sphingomyelinase activity has been associated with human colorectal neoplasms. The aim of this study
was to analyze the alkaline sphingomyelinase activity in feces from healthy subjects and colorectal adenocarcinoma patients
and to correlate it with the enzyme activity in intestinal tissues.
Materials and Methods: The enzyme activity was measured both in the intestinal samples from 12 healthy controls and 51 patients
with colorectal adenocarcinoma (tumoral and paratumoral tissue) and in the fecal samples of 34 healthy subjects and 29 patients
with adenocarcinoma. The relation between sphingomyelinase activity and Dukes' stage, cell differentiation degree, age, and
gender was also analyzed.
Results: Alkaline sphingomyelinase was significantly decreased ( P < 0.001; mean reduction >90%) in tumoral intestinal mucosa of patients compared with controls independently of Dukes' stage
and tumor differentiation grade. Interestingly, the enzyme activity in histologically normal paratumoral tissues was statistically
lower than control samples ( P < 0.001). As occurs in neoplastic tissues, a relevant mean reduction ( P < 0.0001; almost 90%) of alkaline sphingomyelinase was revealed in stool samples from tumor patients when compared with controls.
Conclusion: These findings may have implications for cancer biology and perhaps also for the design of clinical test, thus
suggesting that the fecal sphingomyelinase activity could really reflect the human intestinal mucosa enzyme level and could
represent a new marker for human colorectal adenocarcinoma, mainly taking into account its early appearance in intestinal
neoplasms. |
doi_str_mv | 10.1158/1055-9965.EPI-04-0434 |
format | article |
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for the generation of messengers able to trigger the rapid turnover and apoptosis in intestinal epithelial cells. Markedly
reduced mucosal alkaline sphingomyelinase activity has been associated with human colorectal neoplasms. The aim of this study
was to analyze the alkaline sphingomyelinase activity in feces from healthy subjects and colorectal adenocarcinoma patients
and to correlate it with the enzyme activity in intestinal tissues.
Materials and Methods: The enzyme activity was measured both in the intestinal samples from 12 healthy controls and 51 patients
with colorectal adenocarcinoma (tumoral and paratumoral tissue) and in the fecal samples of 34 healthy subjects and 29 patients
with adenocarcinoma. The relation between sphingomyelinase activity and Dukes' stage, cell differentiation degree, age, and
gender was also analyzed.
Results: Alkaline sphingomyelinase was significantly decreased ( P < 0.001; mean reduction >90%) in tumoral intestinal mucosa of patients compared with controls independently of Dukes' stage
and tumor differentiation grade. Interestingly, the enzyme activity in histologically normal paratumoral tissues was statistically
lower than control samples ( P < 0.001). As occurs in neoplastic tissues, a relevant mean reduction ( P < 0.0001; almost 90%) of alkaline sphingomyelinase was revealed in stool samples from tumor patients when compared with controls.
Conclusion: These findings may have implications for cancer biology and perhaps also for the design of clinical test, thus
suggesting that the fecal sphingomyelinase activity could really reflect the human intestinal mucosa enzyme level and could
represent a new marker for human colorectal adenocarcinoma, mainly taking into account its early appearance in intestinal
neoplasms.</description><identifier>ISSN: 1055-9965</identifier><identifier>EISSN: 1538-7755</identifier><identifier>DOI: 10.1158/1055-9965.EPI-04-0434</identifier><identifier>PMID: 15824156</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adenocarcinoma - diagnosis ; Adenocarcinoma - enzymology ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; alkaline sphingomyelinase ; Biological and medical sciences ; Case-Control Studies ; Colorectal Neoplasms - diagnosis ; Colorectal Neoplasms - enzymology ; Colorectal Neoplasms - pathology ; feces ; Feces - enzymology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; intestinal cancer ; Male ; Medical sciences ; Middle Aged ; Sphingomyelin Phosphodiesterase - isolation & purification ; Sphingomyelin Phosphodiesterase - metabolism ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Cancer epidemiology, biomarkers & prevention, 2005-04, Vol.14 (4), p.856-862</ispartof><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-90ff0c80afbeb361dafabeb5c1aa0531c3167df61a4d6de704a7f7b8a17d47e93</citedby><cites>FETCH-LOGICAL-c482t-90ff0c80afbeb361dafabeb5c1aa0531c3167df61a4d6de704a7f7b8a17d47e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16697868$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15824156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DI MARZIO, Luisa</creatorcontrib><creatorcontrib>DI LEO, Alfredo</creatorcontrib><creatorcontrib>CIFONE, Maria Grazia</creatorcontrib><creatorcontrib>CINQUE, Benedetta</creatorcontrib><creatorcontrib>FANINI, Donatella</creatorcontrib><creatorcontrib>AGNIFILI, Alessio</creatorcontrib><creatorcontrib>BERLOCO, Pasquale</creatorcontrib><creatorcontrib>LINSALATA, Michele</creatorcontrib><creatorcontrib>LORUSSO, Dionigi</creatorcontrib><creatorcontrib>BARONE, Michele</creatorcontrib><creatorcontrib>DE SIMONE, Claudio</creatorcontrib><title>Detection of Alkaline Sphingomyelinase Activity in Human Stool: Proposed Role as a New Diagnostic and Prognostic Marker of Colorectal Cancer</title><title>Cancer epidemiology, biomarkers & prevention</title><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><description>Objectives: Intestinal alkaline sphingomyelinase, by exerting a major role in dietary sphingomyelin digestion, is responsible
for the generation of messengers able to trigger the rapid turnover and apoptosis in intestinal epithelial cells. Markedly
reduced mucosal alkaline sphingomyelinase activity has been associated with human colorectal neoplasms. The aim of this study
was to analyze the alkaline sphingomyelinase activity in feces from healthy subjects and colorectal adenocarcinoma patients
and to correlate it with the enzyme activity in intestinal tissues.
Materials and Methods: The enzyme activity was measured both in the intestinal samples from 12 healthy controls and 51 patients
with colorectal adenocarcinoma (tumoral and paratumoral tissue) and in the fecal samples of 34 healthy subjects and 29 patients
with adenocarcinoma. The relation between sphingomyelinase activity and Dukes' stage, cell differentiation degree, age, and
gender was also analyzed.
Results: Alkaline sphingomyelinase was significantly decreased ( P < 0.001; mean reduction >90%) in tumoral intestinal mucosa of patients compared with controls independently of Dukes' stage
and tumor differentiation grade. Interestingly, the enzyme activity in histologically normal paratumoral tissues was statistically
lower than control samples ( P < 0.001). As occurs in neoplastic tissues, a relevant mean reduction ( P < 0.0001; almost 90%) of alkaline sphingomyelinase was revealed in stool samples from tumor patients when compared with controls.
Conclusion: These findings may have implications for cancer biology and perhaps also for the design of clinical test, thus
suggesting that the fecal sphingomyelinase activity could really reflect the human intestinal mucosa enzyme level and could
represent a new marker for human colorectal adenocarcinoma, mainly taking into account its early appearance in intestinal
neoplasms.</description><subject>Adenocarcinoma - diagnosis</subject><subject>Adenocarcinoma - enzymology</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>alkaline sphingomyelinase</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Colorectal Neoplasms - diagnosis</subject><subject>Colorectal Neoplasms - enzymology</subject><subject>Colorectal Neoplasms - pathology</subject><subject>feces</subject><subject>Feces - enzymology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>intestinal cancer</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Sphingomyelin Phosphodiesterase - isolation & purification</subject><subject>Sphingomyelin Phosphodiesterase - metabolism</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>1055-9965</issn><issn>1538-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpFkd1uEzEQhVcIRH_gEUC-Aa622Fn_7HIXpS2tVKCicG1NvOPE1GsHe0OVd-Ch8ZJUlSx5RvpmjuacqnrD6Bljov3IqBB110lxdnF7XVNeXsOfVcdMNG2tlBDPS_3IHFUnOf-ilKpOiJfVUVkw40zI4-rvOY5oRhcDiZbM_T14F5DcbdYurOKww9JCRjIvzB837ogL5Go7QCB3Y4z-E7lNcRMz9uR79EggEyBf8YGcO1iFmEdnCIR-oh7bL5DuMU1qi-hjKuLgyQKCwfSqemHBZ3x9-E-rn5cXPxZX9c23z9eL-U1teDsb645aS01LwS5x2UjWg4VSCcMAqGiYaZhUvZUMeC97VJSDsmrZAlM9V9g1p9X7_d5Nir-3mEc9uGzQewgYt1lLpZpmJlgBxR40Keac0OpNcgOknWZUTzHoyWI9WaxLDJpyPcVQ5t4eBLbLAfunqYPvBXh3ACAb8DaV-11-4qTsVCvbwn3Yc2u3Wj-4hNr8dyphRkhmrRnXXLdl4z9EsKD8</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>DI MARZIO, Luisa</creator><creator>DI LEO, Alfredo</creator><creator>CIFONE, Maria Grazia</creator><creator>CINQUE, Benedetta</creator><creator>FANINI, Donatella</creator><creator>AGNIFILI, Alessio</creator><creator>BERLOCO, Pasquale</creator><creator>LINSALATA, Michele</creator><creator>LORUSSO, Dionigi</creator><creator>BARONE, Michele</creator><creator>DE SIMONE, Claudio</creator><general>American Association for Cancer Research</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>20050401</creationdate><title>Detection of Alkaline Sphingomyelinase Activity in Human Stool: Proposed Role as a New Diagnostic and Prognostic Marker of Colorectal Cancer</title><author>DI MARZIO, Luisa ; DI LEO, Alfredo ; CIFONE, Maria Grazia ; CINQUE, Benedetta ; FANINI, Donatella ; AGNIFILI, Alessio ; BERLOCO, Pasquale ; LINSALATA, Michele ; LORUSSO, Dionigi ; BARONE, Michele ; DE SIMONE, Claudio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-90ff0c80afbeb361dafabeb5c1aa0531c3167df61a4d6de704a7f7b8a17d47e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adenocarcinoma - diagnosis</topic><topic>Adenocarcinoma - enzymology</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>alkaline sphingomyelinase</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Colorectal Neoplasms - diagnosis</topic><topic>Colorectal Neoplasms - enzymology</topic><topic>Colorectal Neoplasms - pathology</topic><topic>feces</topic><topic>Feces - enzymology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>intestinal cancer</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Sphingomyelin Phosphodiesterase - isolation & purification</topic><topic>Sphingomyelin Phosphodiesterase - metabolism</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DI MARZIO, Luisa</creatorcontrib><creatorcontrib>DI LEO, Alfredo</creatorcontrib><creatorcontrib>CIFONE, Maria Grazia</creatorcontrib><creatorcontrib>CINQUE, Benedetta</creatorcontrib><creatorcontrib>FANINI, Donatella</creatorcontrib><creatorcontrib>AGNIFILI, Alessio</creatorcontrib><creatorcontrib>BERLOCO, Pasquale</creatorcontrib><creatorcontrib>LINSALATA, Michele</creatorcontrib><creatorcontrib>LORUSSO, Dionigi</creatorcontrib><creatorcontrib>BARONE, Michele</creatorcontrib><creatorcontrib>DE SIMONE, Claudio</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>Cancer epidemiology, biomarkers & prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DI MARZIO, Luisa</au><au>DI LEO, Alfredo</au><au>CIFONE, Maria Grazia</au><au>CINQUE, Benedetta</au><au>FANINI, Donatella</au><au>AGNIFILI, Alessio</au><au>BERLOCO, Pasquale</au><au>LINSALATA, Michele</au><au>LORUSSO, Dionigi</au><au>BARONE, Michele</au><au>DE SIMONE, Claudio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Alkaline Sphingomyelinase Activity in Human Stool: Proposed Role as a New Diagnostic and Prognostic Marker of Colorectal Cancer</atitle><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><date>2005-04-01</date><risdate>2005</risdate><volume>14</volume><issue>4</issue><spage>856</spage><epage>862</epage><pages>856-862</pages><issn>1055-9965</issn><eissn>1538-7755</eissn><abstract>Objectives: Intestinal alkaline sphingomyelinase, by exerting a major role in dietary sphingomyelin digestion, is responsible
for the generation of messengers able to trigger the rapid turnover and apoptosis in intestinal epithelial cells. Markedly
reduced mucosal alkaline sphingomyelinase activity has been associated with human colorectal neoplasms. The aim of this study
was to analyze the alkaline sphingomyelinase activity in feces from healthy subjects and colorectal adenocarcinoma patients
and to correlate it with the enzyme activity in intestinal tissues.
Materials and Methods: The enzyme activity was measured both in the intestinal samples from 12 healthy controls and 51 patients
with colorectal adenocarcinoma (tumoral and paratumoral tissue) and in the fecal samples of 34 healthy subjects and 29 patients
with adenocarcinoma. The relation between sphingomyelinase activity and Dukes' stage, cell differentiation degree, age, and
gender was also analyzed.
Results: Alkaline sphingomyelinase was significantly decreased ( P < 0.001; mean reduction >90%) in tumoral intestinal mucosa of patients compared with controls independently of Dukes' stage
and tumor differentiation grade. Interestingly, the enzyme activity in histologically normal paratumoral tissues was statistically
lower than control samples ( P < 0.001). As occurs in neoplastic tissues, a relevant mean reduction ( P < 0.0001; almost 90%) of alkaline sphingomyelinase was revealed in stool samples from tumor patients when compared with controls.
Conclusion: These findings may have implications for cancer biology and perhaps also for the design of clinical test, thus
suggesting that the fecal sphingomyelinase activity could really reflect the human intestinal mucosa enzyme level and could
represent a new marker for human colorectal adenocarcinoma, mainly taking into account its early appearance in intestinal
neoplasms.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>15824156</pmid><doi>10.1158/1055-9965.EPI-04-0434</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | EZB Electronic Journals Library |
subjects | Adenocarcinoma - diagnosis Adenocarcinoma - enzymology Adenocarcinoma - pathology Adult Aged Aged, 80 and over alkaline sphingomyelinase Biological and medical sciences Case-Control Studies Colorectal Neoplasms - diagnosis Colorectal Neoplasms - enzymology Colorectal Neoplasms - pathology feces Feces - enzymology Female Gastroenterology. Liver. Pancreas. Abdomen Humans intestinal cancer Male Medical sciences Middle Aged Sphingomyelin Phosphodiesterase - isolation & purification Sphingomyelin Phosphodiesterase - metabolism Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Detection of Alkaline Sphingomyelinase Activity in Human Stool: Proposed Role as a New Diagnostic and Prognostic Marker of Colorectal Cancer |
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