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Serum heat shock protein 27 levels in patients with hepatocellular carcinoma
Levels of serum heat shock protein 27 (sHsp27) have been studied in numerous cancer types, but their potential relevance in patients with hepatocellular carcinoma (HCC) is undetermined. Our aim was to compare sHsp27 levels in patients with HCC and HCC-free controls. Specifically, we recruited 71 pat...
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Published in: | Cell stress & chaperones 2013-03, Vol.18 (2), p.235-241 |
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creator | Gruden, Gabriella Carucci, Patrizia Lolli, Valentina Cosso, Loretta Dellavalle, Erika Rolle, Emanuela Cantamessa, Alessandro Pinach, Silvia Abate, Maria Lorena Campra, Donata Brunello, Franco Bruno, Graziella Rizzetto, Mario Perin, Paolo Cavallo |
description | Levels of serum heat shock protein 27 (sHsp27) have been studied in numerous cancer types, but their potential relevance in patients with hepatocellular carcinoma (HCC) is undetermined. Our aim was to compare sHsp27 levels in patients with HCC and HCC-free controls. Specifically, we recruited 71 patients with HCC (80 % with early tumour), 80 patients with chronic liver disease (59 with liver cirrhosis and 21 with chronic active hepatitis) and 42 healthy subjects. sHsp27 was measured by immunoenzymatic assay. Results showed that sHsp27 levels were significantly (p |
doi_str_mv | 10.1007/s12192-012-0377-8 |
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Our aim was to compare sHsp27 levels in patients with HCC and HCC-free controls. Specifically, we recruited 71 patients with HCC (80 % with early tumour), 80 patients with chronic liver disease (59 with liver cirrhosis and 21 with chronic active hepatitis) and 42 healthy subjects. sHsp27 was measured by immunoenzymatic assay. Results showed that sHsp27 levels were significantly (p<0.001) higher in patients with HCC than in the other groups, particularly in those with hepatitis C virus (HCV)-related disease. In HCC patients, sHsp27 levels were not associated with prognostic risk factors, such as size/multiplicity of nodules and stage. In logistic regression analysis, performed in patients with liver disease, log-sHsp27 was associated with a significant age-adjusted 2.5-fold increased odds ratio of HCC and with a significant 4.4-fold higher odds ratio of HCC in the subgroup with HCV-related liver disease. In receiver operating characteristic curve analysis, sensitivity and specificity of the best sHsp27 cut-off value (456.5 pg/ml) for differentiating patients with HCC from those with HCC-free chronic liver disease were 70 and 73 %, respectively. In conclusion, sHsp27 levels are enhanced in patients with HCC and may represent a candidate biomarker of HCC.</description><identifier>ISSN: 1355-8145</identifier><identifier>EISSN: 1466-1268</identifier><identifier>DOI: 10.1007/s12192-012-0377-8</identifier><identifier>PMID: 23073653</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Aged ; alpha-Fetoproteins - analysis ; Biochemistry ; Biological markers ; Biomedical and Life Sciences ; Biomedicine ; Cancer ; Cancer Research ; Carcinoma, Hepatocellular - blood ; Carcinoma, Hepatocellular - etiology ; Carcinoma, Hepatocellular - pathology ; Cell Biology ; Female ; Heat shock proteins ; Hepatitis ; Hepatitis C - blood ; Hepatitis C - complications ; Hepatitis C - pathology ; Hepatocellular carcinoma ; HSP27 Heat-Shock Proteins - blood ; Humans ; Immunology ; Liver ; Liver cirrhosis ; Liver Cirrhosis - blood ; Liver Cirrhosis - pathology ; Liver diseases ; Liver Diseases - blood ; Liver Diseases - pathology ; Liver Neoplasms - blood ; Liver Neoplasms - etiology ; Liver Neoplasms - pathology ; Male ; Middle Aged ; Neoplasia ; Neoplasm Staging ; Neurosciences ; Nodules ; Odds Ratio ; Original Paper ; Peptide Fragments - blood ; Prognosis ; Prothrombin ; Risk Factors ; ROC Curve ; Severity of Illness Index</subject><ispartof>Cell stress & chaperones, 2013-03, Vol.18 (2), p.235-241</ispartof><rights>Cell Stress Society International 2013</rights><rights>Cell Stress Society International 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c492t-110b1f4d5c13b2d269d9b5e4d52a254cab0e696d86d76de1708c4fe0ea7685dd3</citedby><cites>FETCH-LOGICAL-c492t-110b1f4d5c13b2d269d9b5e4d52a254cab0e696d86d76de1708c4fe0ea7685dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23610176$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23610176$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791,58236,58469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23073653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gruden, Gabriella</creatorcontrib><creatorcontrib>Carucci, Patrizia</creatorcontrib><creatorcontrib>Lolli, Valentina</creatorcontrib><creatorcontrib>Cosso, Loretta</creatorcontrib><creatorcontrib>Dellavalle, Erika</creatorcontrib><creatorcontrib>Rolle, Emanuela</creatorcontrib><creatorcontrib>Cantamessa, Alessandro</creatorcontrib><creatorcontrib>Pinach, Silvia</creatorcontrib><creatorcontrib>Abate, Maria Lorena</creatorcontrib><creatorcontrib>Campra, Donata</creatorcontrib><creatorcontrib>Brunello, Franco</creatorcontrib><creatorcontrib>Bruno, Graziella</creatorcontrib><creatorcontrib>Rizzetto, Mario</creatorcontrib><creatorcontrib>Perin, Paolo Cavallo</creatorcontrib><title>Serum heat shock protein 27 levels in patients with hepatocellular carcinoma</title><title>Cell stress & chaperones</title><addtitle>Cell Stress and Chaperones</addtitle><addtitle>Cell Stress Chaperones</addtitle><description>Levels of serum heat shock protein 27 (sHsp27) have been studied in numerous cancer types, but their potential relevance in patients with hepatocellular carcinoma (HCC) is undetermined. Our aim was to compare sHsp27 levels in patients with HCC and HCC-free controls. Specifically, we recruited 71 patients with HCC (80 % with early tumour), 80 patients with chronic liver disease (59 with liver cirrhosis and 21 with chronic active hepatitis) and 42 healthy subjects. sHsp27 was measured by immunoenzymatic assay. Results showed that sHsp27 levels were significantly (p<0.001) higher in patients with HCC than in the other groups, particularly in those with hepatitis C virus (HCV)-related disease. In HCC patients, sHsp27 levels were not associated with prognostic risk factors, such as size/multiplicity of nodules and stage. In logistic regression analysis, performed in patients with liver disease, log-sHsp27 was associated with a significant age-adjusted 2.5-fold increased odds ratio of HCC and with a significant 4.4-fold higher odds ratio of HCC in the subgroup with HCV-related liver disease. In receiver operating characteristic curve analysis, sensitivity and specificity of the best sHsp27 cut-off value (456.5 pg/ml) for differentiating patients with HCC from those with HCC-free chronic liver disease were 70 and 73 %, respectively. In conclusion, sHsp27 levels are enhanced in patients with HCC and may represent a candidate biomarker of HCC.</description><subject>Aged</subject><subject>alpha-Fetoproteins - analysis</subject><subject>Biochemistry</subject><subject>Biological markers</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Carcinoma, Hepatocellular - blood</subject><subject>Carcinoma, Hepatocellular - etiology</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Cell Biology</subject><subject>Female</subject><subject>Heat shock proteins</subject><subject>Hepatitis</subject><subject>Hepatitis C - blood</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - pathology</subject><subject>Hepatocellular carcinoma</subject><subject>HSP27 Heat-Shock Proteins - blood</subject><subject>Humans</subject><subject>Immunology</subject><subject>Liver</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - blood</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver diseases</subject><subject>Liver Diseases - blood</subject><subject>Liver Diseases - pathology</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - etiology</subject><subject>Liver Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasia</subject><subject>Neoplasm Staging</subject><subject>Neurosciences</subject><subject>Nodules</subject><subject>Odds Ratio</subject><subject>Original Paper</subject><subject>Peptide Fragments - blood</subject><subject>Prognosis</subject><subject>Prothrombin</subject><subject>Risk Factors</subject><subject>ROC Curve</subject><subject>Severity of Illness Index</subject><issn>1355-8145</issn><issn>1466-1268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kUtP3DAUha0KVCjtD2DRKhKbbgK-dvzIphJCfUkjsaBdW459h8mQxFM7GdR_Xw-haGDBwrKv_Z3je3UIOQV6DpSqiwQMalZSyIsrVeo35BgqKUtgUh_kMxei1FCJI_IupTXNGqXgLTlinCouBT8mixuMU1-s0I5FWgV3V2xiGLEdCqaKDrfYpSIXGzu2OIypuG_HVaZzHRx23dTZWDgbXTuE3r4nh0vbJfzwuJ-Q39--_rr6US6uv_-8ulyUrqrZWALQBpaVFw54wzyTta8bgfmCWSYqZxuKspZeS6-kR1BUu2qJFK2SWnjPT8iX2XczNT16lzuLtjOb2PY2_jXBtub5y9CuzG3YGi40SA7Z4POjQQx_Jkyj6du0m8cOGKZkgAPTXHPFMnr2Al2HKQ55vAeqolSyOlMwUy6GlCIun5oBanZZmTkrk7Myu6yMzppP-1M8Kf6HkwE2Ayk_DbcY975-xfXjLFqnMcQ9UwkUlOT_AIGgqSA</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>Gruden, Gabriella</creator><creator>Carucci, Patrizia</creator><creator>Lolli, Valentina</creator><creator>Cosso, Loretta</creator><creator>Dellavalle, Erika</creator><creator>Rolle, Emanuela</creator><creator>Cantamessa, Alessandro</creator><creator>Pinach, Silvia</creator><creator>Abate, Maria Lorena</creator><creator>Campra, Donata</creator><creator>Brunello, Franco</creator><creator>Bruno, Graziella</creator><creator>Rizzetto, Mario</creator><creator>Perin, Paolo Cavallo</creator><general>Springer</general><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130301</creationdate><title>Serum heat shock protein 27 levels in patients with hepatocellular carcinoma</title><author>Gruden, Gabriella ; Carucci, Patrizia ; Lolli, Valentina ; Cosso, Loretta ; Dellavalle, Erika ; Rolle, Emanuela ; Cantamessa, Alessandro ; Pinach, Silvia ; Abate, Maria Lorena ; Campra, Donata ; Brunello, Franco ; Bruno, Graziella ; Rizzetto, Mario ; Perin, Paolo Cavallo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c492t-110b1f4d5c13b2d269d9b5e4d52a254cab0e696d86d76de1708c4fe0ea7685dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>alpha-Fetoproteins - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell stress & chaperones</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gruden, Gabriella</au><au>Carucci, Patrizia</au><au>Lolli, Valentina</au><au>Cosso, Loretta</au><au>Dellavalle, Erika</au><au>Rolle, Emanuela</au><au>Cantamessa, Alessandro</au><au>Pinach, Silvia</au><au>Abate, Maria Lorena</au><au>Campra, Donata</au><au>Brunello, Franco</au><au>Bruno, Graziella</au><au>Rizzetto, Mario</au><au>Perin, Paolo Cavallo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum heat shock protein 27 levels in patients with hepatocellular carcinoma</atitle><jtitle>Cell stress & chaperones</jtitle><stitle>Cell Stress and Chaperones</stitle><addtitle>Cell Stress Chaperones</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>18</volume><issue>2</issue><spage>235</spage><epage>241</epage><pages>235-241</pages><issn>1355-8145</issn><eissn>1466-1268</eissn><abstract>Levels of serum heat shock protein 27 (sHsp27) have been studied in numerous cancer types, but their potential relevance in patients with hepatocellular carcinoma (HCC) is undetermined. Our aim was to compare sHsp27 levels in patients with HCC and HCC-free controls. Specifically, we recruited 71 patients with HCC (80 % with early tumour), 80 patients with chronic liver disease (59 with liver cirrhosis and 21 with chronic active hepatitis) and 42 healthy subjects. sHsp27 was measured by immunoenzymatic assay. Results showed that sHsp27 levels were significantly (p<0.001) higher in patients with HCC than in the other groups, particularly in those with hepatitis C virus (HCV)-related disease. In HCC patients, sHsp27 levels were not associated with prognostic risk factors, such as size/multiplicity of nodules and stage. In logistic regression analysis, performed in patients with liver disease, log-sHsp27 was associated with a significant age-adjusted 2.5-fold increased odds ratio of HCC and with a significant 4.4-fold higher odds ratio of HCC in the subgroup with HCV-related liver disease. In receiver operating characteristic curve analysis, sensitivity and specificity of the best sHsp27 cut-off value (456.5 pg/ml) for differentiating patients with HCC from those with HCC-free chronic liver disease were 70 and 73 %, respectively. In conclusion, sHsp27 levels are enhanced in patients with HCC and may represent a candidate biomarker of HCC.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>23073653</pmid><doi>10.1007/s12192-012-0377-8</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged alpha-Fetoproteins - analysis Biochemistry Biological markers Biomedical and Life Sciences Biomedicine Cancer Cancer Research Carcinoma, Hepatocellular - blood Carcinoma, Hepatocellular - etiology Carcinoma, Hepatocellular - pathology Cell Biology Female Heat shock proteins Hepatitis Hepatitis C - blood Hepatitis C - complications Hepatitis C - pathology Hepatocellular carcinoma HSP27 Heat-Shock Proteins - blood Humans Immunology Liver Liver cirrhosis Liver Cirrhosis - blood Liver Cirrhosis - pathology Liver diseases Liver Diseases - blood Liver Diseases - pathology Liver Neoplasms - blood Liver Neoplasms - etiology Liver Neoplasms - pathology Male Middle Aged Neoplasia Neoplasm Staging Neurosciences Nodules Odds Ratio Original Paper Peptide Fragments - blood Prognosis Prothrombin Risk Factors ROC Curve Severity of Illness Index |
title | Serum heat shock protein 27 levels in patients with hepatocellular carcinoma |
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