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Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer
The exact molecular background and the connection between protein and mRNA expression in colorectal cancer (CRC) development and progression are not completely elucidated. Our purposes were the identification of protein markers of colorectal carcinogenesis and progression using protein arrays and va...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833602/ https://www.ncbi.nlm.nih.gov/pubmed/20164542 http://dx.doi.org/10.3233/DMA-2010-0677 |
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author | Spisák, Sándor Galamb, Barnabás Sipos, Ferenc Galamb, Orsolya Wichmann, Barnabás Solymosi, Norbert Nemes, Balázs Molnár, Jeannette Tulassay, Zsolt Molnár, Béla |
author_facet | Spisák, Sándor Galamb, Barnabás Sipos, Ferenc Galamb, Orsolya Wichmann, Barnabás Solymosi, Norbert Nemes, Balázs Molnár, Jeannette Tulassay, Zsolt Molnár, Béla |
author_sort | Spisák, Sándor |
collection | PubMed |
description | The exact molecular background and the connection between protein and mRNA expression in colorectal cancer (CRC) development and progression are not completely elucidated. Our purposes were the identification of protein markers of colorectal carcinogenesis and progression using protein arrays and validation on tissue microarrays. The connection between antibody and mRNA expression array results was also examined. Using cancerous and adjacent normal samples from 10 patients with early and 6 with advanced CRC, 67 differentially expressed genes were identified between normal and cancerous samples. A marker set containing 6 proteins (CCNA1, AR, TOP1, TGFB, HSP60, ERK1) was developed which could differentiate normal specimen, early and late stage CRC with high sensitivity and specificity. Dukes D stage samples were analyzed on HGU133plus2.0 microarrays. In these samples, mRNA and protein expression of 143 genes showed strong positive correlations (R(2) > 0.8), while a negative correlation (R(2) > 0.9) was found in case of 95 genes. Based on our results a correlation could be established between transcriptome and antibody array results, hence the former may be used as a high-capacity screening method before applying antibody arrays containing already planned targets. Antibody microarrays may have a fundamental importance in testing of marker combinations and future application in diagnostics of tumorous diseases. |
format | Online Article Text |
id | pubmed-3833602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38336022013-12-17 Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer Spisák, Sándor Galamb, Barnabás Sipos, Ferenc Galamb, Orsolya Wichmann, Barnabás Solymosi, Norbert Nemes, Balázs Molnár, Jeannette Tulassay, Zsolt Molnár, Béla Dis Markers Other The exact molecular background and the connection between protein and mRNA expression in colorectal cancer (CRC) development and progression are not completely elucidated. Our purposes were the identification of protein markers of colorectal carcinogenesis and progression using protein arrays and validation on tissue microarrays. The connection between antibody and mRNA expression array results was also examined. Using cancerous and adjacent normal samples from 10 patients with early and 6 with advanced CRC, 67 differentially expressed genes were identified between normal and cancerous samples. A marker set containing 6 proteins (CCNA1, AR, TOP1, TGFB, HSP60, ERK1) was developed which could differentiate normal specimen, early and late stage CRC with high sensitivity and specificity. Dukes D stage samples were analyzed on HGU133plus2.0 microarrays. In these samples, mRNA and protein expression of 143 genes showed strong positive correlations (R(2) > 0.8), while a negative correlation (R(2) > 0.9) was found in case of 95 genes. Based on our results a correlation could be established between transcriptome and antibody array results, hence the former may be used as a high-capacity screening method before applying antibody arrays containing already planned targets. Antibody microarrays may have a fundamental importance in testing of marker combinations and future application in diagnostics of tumorous diseases. IOS Press 2010 2010-02-17 /pmc/articles/PMC3833602/ /pubmed/20164542 http://dx.doi.org/10.3233/DMA-2010-0677 Text en Copyright © 2010 Hindawi Publishing Corporation. |
spellingShingle | Other Spisák, Sándor Galamb, Barnabás Sipos, Ferenc Galamb, Orsolya Wichmann, Barnabás Solymosi, Norbert Nemes, Balázs Molnár, Jeannette Tulassay, Zsolt Molnár, Béla Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer |
title | Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer |
title_full | Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer |
title_fullStr | Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer |
title_full_unstemmed | Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer |
title_short | Applicability of Antibody and mRNA Expression Microarrays for Identifying Diagnostic and Progression Markers of Early and Late Stage Colorectal Cancer |
title_sort | applicability of antibody and mrna expression microarrays for identifying diagnostic and progression markers of early and late stage colorectal cancer |
topic | Other |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833602/ https://www.ncbi.nlm.nih.gov/pubmed/20164542 http://dx.doi.org/10.3233/DMA-2010-0677 |
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