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Genomic and oncoproteomic advances in detection and treatment of colorectal cancer

AIMS: We will examine the latest advances in genomic and proteomic laboratory technology. Through an extensive literature review we aim to critically appraise those studies which have utilized these latest technologies and ascertain their potential to identify clinically useful biomarkers. METHODS:...

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Autores principales: McHugh, Seamus M, O'Donnell, Jill, Gillen, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667518/
https://www.ncbi.nlm.nih.gov/pubmed/19338662
http://dx.doi.org/10.1186/1477-7819-7-36
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author McHugh, Seamus M
O'Donnell, Jill
Gillen, Peter
author_facet McHugh, Seamus M
O'Donnell, Jill
Gillen, Peter
author_sort McHugh, Seamus M
collection PubMed
description AIMS: We will examine the latest advances in genomic and proteomic laboratory technology. Through an extensive literature review we aim to critically appraise those studies which have utilized these latest technologies and ascertain their potential to identify clinically useful biomarkers. METHODS: An extensive review of the literature was carried out in both online medical journals and through the Royal College of Surgeons in Ireland library. RESULTS: Laboratory technology has advanced in the fields of genomics and oncoproteomics. Gene expression profiling with DNA microarray technology has allowed us to begin genetic profiling of colorectal cancer tissue. The response to chemotherapy can differ amongst individual tumors. For the first time researchers have begun to isolate and identify the genes responsible. New laboratory techniques allow us to isolate proteins preferentially expressed in colorectal cancer tissue. This could potentially lead to identification of a clinically useful protein biomarker in colorectal cancer screening and treatment. CONCLUSION: If a set of discriminating genes could be used for characterization and prediction of chemotherapeutic response, an individualized tailored therapeutic regime could become the standard of care for those undergoing systemic treatment for colorectal cancer. New laboratory techniques of protein identification may eventually allow identification of a clinically useful biomarker that could be used for screening and treatment. At present however, both expression of different gene signatures and isolation of various protein peaks has been limited by study size. Independent multi-centre correlation of results with larger sample sizes is needed to allow translation into clinical practice.
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spelling pubmed-26675182009-04-10 Genomic and oncoproteomic advances in detection and treatment of colorectal cancer McHugh, Seamus M O'Donnell, Jill Gillen, Peter World J Surg Oncol Review AIMS: We will examine the latest advances in genomic and proteomic laboratory technology. Through an extensive literature review we aim to critically appraise those studies which have utilized these latest technologies and ascertain their potential to identify clinically useful biomarkers. METHODS: An extensive review of the literature was carried out in both online medical journals and through the Royal College of Surgeons in Ireland library. RESULTS: Laboratory technology has advanced in the fields of genomics and oncoproteomics. Gene expression profiling with DNA microarray technology has allowed us to begin genetic profiling of colorectal cancer tissue. The response to chemotherapy can differ amongst individual tumors. For the first time researchers have begun to isolate and identify the genes responsible. New laboratory techniques allow us to isolate proteins preferentially expressed in colorectal cancer tissue. This could potentially lead to identification of a clinically useful protein biomarker in colorectal cancer screening and treatment. CONCLUSION: If a set of discriminating genes could be used for characterization and prediction of chemotherapeutic response, an individualized tailored therapeutic regime could become the standard of care for those undergoing systemic treatment for colorectal cancer. New laboratory techniques of protein identification may eventually allow identification of a clinically useful biomarker that could be used for screening and treatment. At present however, both expression of different gene signatures and isolation of various protein peaks has been limited by study size. Independent multi-centre correlation of results with larger sample sizes is needed to allow translation into clinical practice. BioMed Central 2009-04-01 /pmc/articles/PMC2667518/ /pubmed/19338662 http://dx.doi.org/10.1186/1477-7819-7-36 Text en Copyright © 2009 McHugh et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
McHugh, Seamus M
O'Donnell, Jill
Gillen, Peter
Genomic and oncoproteomic advances in detection and treatment of colorectal cancer
title Genomic and oncoproteomic advances in detection and treatment of colorectal cancer
title_full Genomic and oncoproteomic advances in detection and treatment of colorectal cancer
title_fullStr Genomic and oncoproteomic advances in detection and treatment of colorectal cancer
title_full_unstemmed Genomic and oncoproteomic advances in detection and treatment of colorectal cancer
title_short Genomic and oncoproteomic advances in detection and treatment of colorectal cancer
title_sort genomic and oncoproteomic advances in detection and treatment of colorectal cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667518/
https://www.ncbi.nlm.nih.gov/pubmed/19338662
http://dx.doi.org/10.1186/1477-7819-7-36
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