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Identification of Apo-A1 as a biomarker for early diagnosis of bladder transitional cell carcinoma
Bladder transitional cell carcinoma (BTCC) is the fourth most frequent neoplasia in men, clinically characterized by high recurrent rates and poor prognosis. Availability of urinary tumor biomarkers represents a convenient alternative for early detection and disease surveillance because of its direc...
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Published in: | Proteome science 2011-04, Vol.9 (1), p.21-21, Article 21 |
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description | Bladder transitional cell carcinoma (BTCC) is the fourth most frequent neoplasia in men, clinically characterized by high recurrent rates and poor prognosis. Availability of urinary tumor biomarkers represents a convenient alternative for early detection and disease surveillance because of its direct contact with the tumor and sample accessibility.
We tested urine samples from healthy volunteers and patients with low malignant or aggressive BTCC to identify potential biomarkers for early detection of BTCC by two-dimensional electrophoresis (2-DE) coupled with mass spectrometry (MS) and bioinformatics analysis. We observed increased expression of five proteins, including fibrinogen (Fb), lactate dehydrogenase B (LDHB), apolipoprotein-A1 (Apo-A1), clusterin (CLU) and haptoglobin (Hp), which were increased in urine samples of patients with low malignant or aggressive bladder cancer. Further analysis of urine samples of aggressive BTCC showed significant increase in Apo-A1 expression compared to low malignant BTCC. Apo-A1 level was measured quantitatively using enzyme-linked immunosorbent assay (ELISA) and was suggested to provide diagnostic utility to distinguish patients with bladder cancer from controls at 18.22 ng/ml, and distinguish patients with low malignant BTCC from patients with aggressive BTCC in two-tie grading system at 29.86 ng/ml respectively. Further validation assay showed that Apo-A1 could be used as a biomarker to diagnosis BTCC with a sensitivity and specificity of 91.6% and 85.7% respectively, and classify BTCC in two-tie grading system with a sensitivity and specificity of 83.7% and 89.7% respectively.
Taken together, our findings suggest Apo-A1 could be a potential biomarker related with early diagnosis and classification in two-tie grading system for bladder cancer. |
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We tested urine samples from healthy volunteers and patients with low malignant or aggressive BTCC to identify potential biomarkers for early detection of BTCC by two-dimensional electrophoresis (2-DE) coupled with mass spectrometry (MS) and bioinformatics analysis. We observed increased expression of five proteins, including fibrinogen (Fb), lactate dehydrogenase B (LDHB), apolipoprotein-A1 (Apo-A1), clusterin (CLU) and haptoglobin (Hp), which were increased in urine samples of patients with low malignant or aggressive bladder cancer. Further analysis of urine samples of aggressive BTCC showed significant increase in Apo-A1 expression compared to low malignant BTCC. Apo-A1 level was measured quantitatively using enzyme-linked immunosorbent assay (ELISA) and was suggested to provide diagnostic utility to distinguish patients with bladder cancer from controls at 18.22 ng/ml, and distinguish patients with low malignant BTCC from patients with aggressive BTCC in two-tie grading system at 29.86 ng/ml respectively. Further validation assay showed that Apo-A1 could be used as a biomarker to diagnosis BTCC with a sensitivity and specificity of 91.6% and 85.7% respectively, and classify BTCC in two-tie grading system with a sensitivity and specificity of 83.7% and 89.7% respectively.
Taken together, our findings suggest Apo-A1 could be a potential biomarker related with early diagnosis and classification in two-tie grading system for bladder cancer.</description><identifier>ISSN: 1477-5956</identifier><identifier>EISSN: 1477-5956</identifier><identifier>DOI: 10.1186/1477-5956-9-21</identifier><identifier>PMID: 21496341</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Bladder cancer ; Care and treatment ; Diagnosis ; Enzyme-linked immunosorbent assay ; Genetic aspects ; Lipoprotein A ; Risk factors</subject><ispartof>Proteome science, 2011-04, Vol.9 (1), p.21-21, Article 21</ispartof><rights>COPYRIGHT 2011 BioMed Central Ltd.</rights><rights>Copyright ©2011 Li et al; licensee BioMed Central Ltd. 2011 Li et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b614t-b7dcf8f9e73fbb7d89b301b8d5e7717fc1db7be44345224eca6a7aee3f1a03373</citedby><cites>FETCH-LOGICAL-b614t-b7dcf8f9e73fbb7d89b301b8d5e7717fc1db7be44345224eca6a7aee3f1a03373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089778/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089778/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21496341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Hongjie</creatorcontrib><creatorcontrib>Li, Changying</creatorcontrib><creatorcontrib>Wu, Huili</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Wang, Jin</creatorcontrib><creatorcontrib>Wang, Shixin</creatorcontrib><creatorcontrib>Chang, Jiwu</creatorcontrib><title>Identification of Apo-A1 as a biomarker for early diagnosis of bladder transitional cell carcinoma</title><title>Proteome science</title><addtitle>Proteome Sci</addtitle><description>Bladder transitional cell carcinoma (BTCC) is the fourth most frequent neoplasia in men, clinically characterized by high recurrent rates and poor prognosis. Availability of urinary tumor biomarkers represents a convenient alternative for early detection and disease surveillance because of its direct contact with the tumor and sample accessibility.
We tested urine samples from healthy volunteers and patients with low malignant or aggressive BTCC to identify potential biomarkers for early detection of BTCC by two-dimensional electrophoresis (2-DE) coupled with mass spectrometry (MS) and bioinformatics analysis. We observed increased expression of five proteins, including fibrinogen (Fb), lactate dehydrogenase B (LDHB), apolipoprotein-A1 (Apo-A1), clusterin (CLU) and haptoglobin (Hp), which were increased in urine samples of patients with low malignant or aggressive bladder cancer. Further analysis of urine samples of aggressive BTCC showed significant increase in Apo-A1 expression compared to low malignant BTCC. Apo-A1 level was measured quantitatively using enzyme-linked immunosorbent assay (ELISA) and was suggested to provide diagnostic utility to distinguish patients with bladder cancer from controls at 18.22 ng/ml, and distinguish patients with low malignant BTCC from patients with aggressive BTCC in two-tie grading system at 29.86 ng/ml respectively. Further validation assay showed that Apo-A1 could be used as a biomarker to diagnosis BTCC with a sensitivity and specificity of 91.6% and 85.7% respectively, and classify BTCC in two-tie grading system with a sensitivity and specificity of 83.7% and 89.7% respectively.
Taken together, our findings suggest Apo-A1 could be a potential biomarker related with early diagnosis and classification in two-tie grading system for bladder cancer.</description><subject>Bladder cancer</subject><subject>Care and treatment</subject><subject>Diagnosis</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Genetic aspects</subject><subject>Lipoprotein A</subject><subject>Risk factors</subject><issn>1477-5956</issn><issn>1477-5956</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptkttrFDEUhwdRbK2--igDPkgfpk7uyYuwFKsLBcHLczi5ramzkzWZLfa_N9OtSxeXQC7n_M7HuaRpXqP-AiHJ3yMqRMcU453qMHrSnO4NTx_dT5oXpdz0PcYK8-fNCUZUcULRaWOWzo9TDNHCFNPYptAuNqlboBZKC62JaQ35l89tSLn1kIe71kVYjanEMovNAM5V95RhLHFGwNBaP9QNso1jDX_ZPAswFP_q4Txrflx9_H75ubv-8ml5ubjuDEd06oxwNsigvCDB1IdUhvTISMe8EEgEi5wRxlNKKMOYegscBHhPAoKeEEHOmuWO6xLc6E2ONfM7nSDqe0PKKw15inbwuhcUCadcCBxT5ShwZiRhUlgUiOllZX3YsTZbs_bO1h5lGA6gh54x_tSrdKtJL5UQM2CxA8wdPA449Ni01vO89DwvrTRGlfHuIYmcfm99mfQ6lrm3MPq0LVpyxqWSjFfl251yBbW6OIZUmXZW6wVmTEiG73O6OKKqy_l1tGn0IVb7QcD5QUDVTP7PtIJtKXr57etRuM2plOzDvlbU6_mr_l_dm8ct3sv__U3yF5G45Ag</recordid><startdate>20110417</startdate><enddate>20110417</enddate><creator>Li, Hongjie</creator><creator>Li, Changying</creator><creator>Wu, Huili</creator><creator>Zhang, Ting</creator><creator>Wang, Jin</creator><creator>Wang, Shixin</creator><creator>Chang, Jiwu</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110417</creationdate><title>Identification of Apo-A1 as a biomarker for early diagnosis of bladder transitional cell carcinoma</title><author>Li, Hongjie ; Li, Changying ; Wu, Huili ; Zhang, Ting ; Wang, Jin ; Wang, Shixin ; Chang, Jiwu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b614t-b7dcf8f9e73fbb7d89b301b8d5e7717fc1db7be44345224eca6a7aee3f1a03373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Bladder cancer</topic><topic>Care and treatment</topic><topic>Diagnosis</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Genetic aspects</topic><topic>Lipoprotein A</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Hongjie</creatorcontrib><creatorcontrib>Li, Changying</creatorcontrib><creatorcontrib>Wu, Huili</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Wang, Jin</creatorcontrib><creatorcontrib>Wang, Shixin</creatorcontrib><creatorcontrib>Chang, Jiwu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Proteome science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Hongjie</au><au>Li, Changying</au><au>Wu, Huili</au><au>Zhang, Ting</au><au>Wang, Jin</au><au>Wang, Shixin</au><au>Chang, Jiwu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Apo-A1 as a biomarker for early diagnosis of bladder transitional cell carcinoma</atitle><jtitle>Proteome science</jtitle><addtitle>Proteome Sci</addtitle><date>2011-04-17</date><risdate>2011</risdate><volume>9</volume><issue>1</issue><spage>21</spage><epage>21</epage><pages>21-21</pages><artnum>21</artnum><issn>1477-5956</issn><eissn>1477-5956</eissn><abstract>Bladder transitional cell carcinoma (BTCC) is the fourth most frequent neoplasia in men, clinically characterized by high recurrent rates and poor prognosis. Availability of urinary tumor biomarkers represents a convenient alternative for early detection and disease surveillance because of its direct contact with the tumor and sample accessibility.
We tested urine samples from healthy volunteers and patients with low malignant or aggressive BTCC to identify potential biomarkers for early detection of BTCC by two-dimensional electrophoresis (2-DE) coupled with mass spectrometry (MS) and bioinformatics analysis. We observed increased expression of five proteins, including fibrinogen (Fb), lactate dehydrogenase B (LDHB), apolipoprotein-A1 (Apo-A1), clusterin (CLU) and haptoglobin (Hp), which were increased in urine samples of patients with low malignant or aggressive bladder cancer. Further analysis of urine samples of aggressive BTCC showed significant increase in Apo-A1 expression compared to low malignant BTCC. Apo-A1 level was measured quantitatively using enzyme-linked immunosorbent assay (ELISA) and was suggested to provide diagnostic utility to distinguish patients with bladder cancer from controls at 18.22 ng/ml, and distinguish patients with low malignant BTCC from patients with aggressive BTCC in two-tie grading system at 29.86 ng/ml respectively. Further validation assay showed that Apo-A1 could be used as a biomarker to diagnosis BTCC with a sensitivity and specificity of 91.6% and 85.7% respectively, and classify BTCC in two-tie grading system with a sensitivity and specificity of 83.7% and 89.7% respectively.
Taken together, our findings suggest Apo-A1 could be a potential biomarker related with early diagnosis and classification in two-tie grading system for bladder cancer.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>21496341</pmid><doi>10.1186/1477-5956-9-21</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bladder cancer Care and treatment Diagnosis Enzyme-linked immunosorbent assay Genetic aspects Lipoprotein A Risk factors |
title | Identification of Apo-A1 as a biomarker for early diagnosis of bladder transitional cell carcinoma |
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