Towards pancreatic cancer diagnosis using EIS biochips
Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers in Europe and the United States. It has a very low 5 years-survival rate and its diagnosis is often late and imprecise due to the lack of specificity of currently used markers for PDAC. As previously demonstrate...
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Veröffentlicht in: | Lab on a chip 2013-01, Vol.13 (4), p.73-734 |
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creator | Chiriacò, Maria Serena Primiceri, Elisabetta Monteduro, Anna Grazia Bove, Anna Leporatti, Stefano Capello, Michela Ferri-Borgogno, Sammy Rinaldi, Ross Novelli, Francesco Maruccio, Giuseppe |
description | Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers in Europe and the United States. It has a very low 5 years-survival rate and its diagnosis is often late and imprecise due to the lack of specificity of currently used markers for PDAC. As previously demonstrated PDAC patients' sera may contain autoantibodies towards phosphorylated α-enolase (ENOA), which in combination with other standard markers can increase specificity in diagnosis of PDAC. In this context we realized a microfluidic platform with integrated EIS biosensors. We achieved a specific antibodies detection by immobilizing onto electrodes peptides corresponding to a portion of ENOA. Phosphorylation of peptides was found to influence the recognition of antibodies in PDAC patients' sera detected by the developed biochip thus validating the EIS technique as a strong tool for quick, cost-saving and label-free analysis of serum samples. Biochip results are in agreement with those from traditional techniques, such as ELISA and western blot, but measurements are much more sensitive and specific, increasing the possibility of PDAC diagnosis. In addition this approach is faster and more reproducible compared to traditional techniques making the developed biochips ideal for a quick, cost-saving and label-free analysis of serum samples.
EIS biochips are reported for label-free detection in serum samples of natural antibodies against Ser-419 phosphorylated residue which are relevant for pancreatic ductal adenocarcinoma early diagnosis. |
doi_str_mv | 10.1039/c2lc41127j |
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EIS biochips are reported for label-free detection in serum samples of natural antibodies against Ser-419 phosphorylated residue which are relevant for pancreatic ductal adenocarcinoma early diagnosis.</description><identifier>ISSN: 1473-0197</identifier><identifier>EISSN: 1473-0189</identifier><identifier>DOI: 10.1039/c2lc41127j</identifier><identifier>PMID: 23287869</identifier><language>eng</language><publisher>England</publisher><subject>Biochips ; Biosensing Techniques - instrumentation ; Biosensing Techniques - methods ; Cancer ; Carcinoma, Pancreatic Ductal - blood ; Carcinoma, Pancreatic Ductal - diagnosis ; Cost analysis ; Diagnosis ; Dielectric Spectroscopy - instrumentation ; Dielectric Spectroscopy - methods ; Electrochemical impedance spectroscopy ; Enzyme-Linked Immunosorbent Assay ; Humans ; Markers ; Pancreatic Neoplasms - blood ; Pancreatic Neoplasms - diagnosis ; Patients ; Peptides</subject><ispartof>Lab on a chip, 2013-01, Vol.13 (4), p.73-734</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-72d821bba1ea067a2d68edf537cf7eb62e99343404093220af82db9a5c9e36c83</citedby><cites>FETCH-LOGICAL-c470t-72d821bba1ea067a2d68edf537cf7eb62e99343404093220af82db9a5c9e36c83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23287869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiriacò, Maria Serena</creatorcontrib><creatorcontrib>Primiceri, Elisabetta</creatorcontrib><creatorcontrib>Monteduro, Anna Grazia</creatorcontrib><creatorcontrib>Bove, Anna</creatorcontrib><creatorcontrib>Leporatti, Stefano</creatorcontrib><creatorcontrib>Capello, Michela</creatorcontrib><creatorcontrib>Ferri-Borgogno, Sammy</creatorcontrib><creatorcontrib>Rinaldi, Ross</creatorcontrib><creatorcontrib>Novelli, Francesco</creatorcontrib><creatorcontrib>Maruccio, Giuseppe</creatorcontrib><title>Towards pancreatic cancer diagnosis using EIS biochips</title><title>Lab on a chip</title><addtitle>Lab Chip</addtitle><description>Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers in Europe and the United States. It has a very low 5 years-survival rate and its diagnosis is often late and imprecise due to the lack of specificity of currently used markers for PDAC. As previously demonstrated PDAC patients' sera may contain autoantibodies towards phosphorylated α-enolase (ENOA), which in combination with other standard markers can increase specificity in diagnosis of PDAC. In this context we realized a microfluidic platform with integrated EIS biosensors. We achieved a specific antibodies detection by immobilizing onto electrodes peptides corresponding to a portion of ENOA. Phosphorylation of peptides was found to influence the recognition of antibodies in PDAC patients' sera detected by the developed biochip thus validating the EIS technique as a strong tool for quick, cost-saving and label-free analysis of serum samples. Biochip results are in agreement with those from traditional techniques, such as ELISA and western blot, but measurements are much more sensitive and specific, increasing the possibility of PDAC diagnosis. In addition this approach is faster and more reproducible compared to traditional techniques making the developed biochips ideal for a quick, cost-saving and label-free analysis of serum samples.
EIS biochips are reported for label-free detection in serum samples of natural antibodies against Ser-419 phosphorylated residue which are relevant for pancreatic ductal adenocarcinoma early diagnosis.</description><subject>Biochips</subject><subject>Biosensing Techniques - instrumentation</subject><subject>Biosensing Techniques - methods</subject><subject>Cancer</subject><subject>Carcinoma, Pancreatic Ductal - blood</subject><subject>Carcinoma, Pancreatic Ductal - diagnosis</subject><subject>Cost analysis</subject><subject>Diagnosis</subject><subject>Dielectric Spectroscopy - instrumentation</subject><subject>Dielectric Spectroscopy - methods</subject><subject>Electrochemical impedance spectroscopy</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Humans</subject><subject>Markers</subject><subject>Pancreatic Neoplasms - blood</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Patients</subject><subject>Peptides</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0EtLw0AUBeBBFFurG_dK3IkQnVfmsSylaqHgwroOk5lJnZImcW6D-O-NtFbc6OoeuB9ncRA6J_iWYKbvLK0sJ4TK1QEaEi5ZionSh_us5QCdAKwwJhkX6hgNKKNKKqGHSCyadxMdJK2pbfRmE2xi--hj4oJZ1g0ESDoI9TKZzp6TIjT2NbRwio5KU4E_290RermfLiaP6fzpYTYZz1PLJd6kkjpFSVEY4g0W0lAnlHdlxqQtpS8E9VozzjjmWDNKsSkVdYU2mdWeCavYCF1ve9vYvHUeNvk6gPVVZWrfdJATRjKREYbZ_5QqirnknPf0ZkttbACiL_M2hrWJHznB-dek-c-kPb7c9XbF2rs9_d6wBxdbEMHuv78Krv76560r2ScRHoUq</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Chiriacò, Maria Serena</creator><creator>Primiceri, Elisabetta</creator><creator>Monteduro, Anna Grazia</creator><creator>Bove, Anna</creator><creator>Leporatti, Stefano</creator><creator>Capello, Michela</creator><creator>Ferri-Borgogno, Sammy</creator><creator>Rinaldi, Ross</creator><creator>Novelli, Francesco</creator><creator>Maruccio, Giuseppe</creator><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><scope>7SP</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>L7M</scope></search><sort><creationdate>20130101</creationdate><title>Towards pancreatic cancer diagnosis using EIS biochips</title><author>Chiriacò, Maria Serena ; Primiceri, Elisabetta ; Monteduro, Anna Grazia ; Bove, Anna ; Leporatti, Stefano ; Capello, Michela ; Ferri-Borgogno, Sammy ; Rinaldi, Ross ; Novelli, Francesco ; Maruccio, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-72d821bba1ea067a2d68edf537cf7eb62e99343404093220af82db9a5c9e36c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biochips</topic><topic>Biosensing Techniques - instrumentation</topic><topic>Biosensing Techniques - methods</topic><topic>Cancer</topic><topic>Carcinoma, Pancreatic Ductal - blood</topic><topic>Carcinoma, Pancreatic Ductal - diagnosis</topic><topic>Cost analysis</topic><topic>Diagnosis</topic><topic>Dielectric Spectroscopy - instrumentation</topic><topic>Dielectric Spectroscopy - methods</topic><topic>Electrochemical impedance spectroscopy</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Humans</topic><topic>Markers</topic><topic>Pancreatic Neoplasms - blood</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Patients</topic><topic>Peptides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiriacò, Maria Serena</creatorcontrib><creatorcontrib>Primiceri, Elisabetta</creatorcontrib><creatorcontrib>Monteduro, Anna Grazia</creatorcontrib><creatorcontrib>Bove, Anna</creatorcontrib><creatorcontrib>Leporatti, Stefano</creatorcontrib><creatorcontrib>Capello, Michela</creatorcontrib><creatorcontrib>Ferri-Borgogno, Sammy</creatorcontrib><creatorcontrib>Rinaldi, Ross</creatorcontrib><creatorcontrib>Novelli, Francesco</creatorcontrib><creatorcontrib>Maruccio, Giuseppe</creatorcontrib><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><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Lab on a chip</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiriacò, Maria Serena</au><au>Primiceri, Elisabetta</au><au>Monteduro, Anna Grazia</au><au>Bove, Anna</au><au>Leporatti, Stefano</au><au>Capello, Michela</au><au>Ferri-Borgogno, Sammy</au><au>Rinaldi, Ross</au><au>Novelli, Francesco</au><au>Maruccio, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Towards pancreatic cancer diagnosis using EIS biochips</atitle><jtitle>Lab on a chip</jtitle><addtitle>Lab Chip</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>13</volume><issue>4</issue><spage>73</spage><epage>734</epage><pages>73-734</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers in Europe and the United States. It has a very low 5 years-survival rate and its diagnosis is often late and imprecise due to the lack of specificity of currently used markers for PDAC. As previously demonstrated PDAC patients' sera may contain autoantibodies towards phosphorylated α-enolase (ENOA), which in combination with other standard markers can increase specificity in diagnosis of PDAC. In this context we realized a microfluidic platform with integrated EIS biosensors. We achieved a specific antibodies detection by immobilizing onto electrodes peptides corresponding to a portion of ENOA. Phosphorylation of peptides was found to influence the recognition of antibodies in PDAC patients' sera detected by the developed biochip thus validating the EIS technique as a strong tool for quick, cost-saving and label-free analysis of serum samples. Biochip results are in agreement with those from traditional techniques, such as ELISA and western blot, but measurements are much more sensitive and specific, increasing the possibility of PDAC diagnosis. In addition this approach is faster and more reproducible compared to traditional techniques making the developed biochips ideal for a quick, cost-saving and label-free analysis of serum samples.
EIS biochips are reported for label-free detection in serum samples of natural antibodies against Ser-419 phosphorylated residue which are relevant for pancreatic ductal adenocarcinoma early diagnosis.</abstract><cop>England</cop><pmid>23287869</pmid><doi>10.1039/c2lc41127j</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biochips Biosensing Techniques - instrumentation Biosensing Techniques - methods Cancer Carcinoma, Pancreatic Ductal - blood Carcinoma, Pancreatic Ductal - diagnosis Cost analysis Diagnosis Dielectric Spectroscopy - instrumentation Dielectric Spectroscopy - methods Electrochemical impedance spectroscopy Enzyme-Linked Immunosorbent Assay Humans Markers Pancreatic Neoplasms - blood Pancreatic Neoplasms - diagnosis Patients Peptides |
title | Towards pancreatic cancer diagnosis using EIS biochips |
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