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High-density tissue microarrays from prostate needle biopsies

BACKGROUND: Formalin-fixed prostate biopsies are frequently the only tissue collected at the time of prostate cancer diagnosis. There is therefore a requirement for techniques that allow the use of these prostate biopsy specimens in a high-throughput analysis of immunohistochemical and fluorescence-...

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Detalles Bibliográficos
Autores principales: McCarthy, F, Dennis, N, Flohr, P, Jhavar, S, Parker, C, Cooper, C S
Formato: Texto
Lenguaje:English
Publicado: BMJ Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002837/
https://www.ncbi.nlm.nih.gov/pubmed/21081515
http://dx.doi.org/10.1136/jcp.2010.082339
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author McCarthy, F
Dennis, N
Flohr, P
Jhavar, S
Parker, C
Cooper, C S
author_facet McCarthy, F
Dennis, N
Flohr, P
Jhavar, S
Parker, C
Cooper, C S
author_sort McCarthy, F
collection PubMed
description BACKGROUND: Formalin-fixed prostate biopsies are frequently the only tissue collected at the time of prostate cancer diagnosis. There is therefore a requirement for techniques that allow the use of these prostate biopsy specimens in a high-throughput analysis of immunohistochemical and fluorescence-in-situ-hybridisation-detected biomarkers. METHODS: The authors have previously described methods that allow tissue microarray (TMA) construction from prostate biopsies. Here, we describe significant technical innovations that provide an easier and more robust system of biopsy–TMA construction. RESULTS AND DISCUSSION: The TMAs produced are of a high density (up to 104 cores each, 8×13) and allow a multiplex analysis of biomarkers in the context of clinical trials.
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spelling pubmed-30028372010-12-23 High-density tissue microarrays from prostate needle biopsies McCarthy, F Dennis, N Flohr, P Jhavar, S Parker, C Cooper, C S J Clin Pathol Short Report BACKGROUND: Formalin-fixed prostate biopsies are frequently the only tissue collected at the time of prostate cancer diagnosis. There is therefore a requirement for techniques that allow the use of these prostate biopsy specimens in a high-throughput analysis of immunohistochemical and fluorescence-in-situ-hybridisation-detected biomarkers. METHODS: The authors have previously described methods that allow tissue microarray (TMA) construction from prostate biopsies. Here, we describe significant technical innovations that provide an easier and more robust system of biopsy–TMA construction. RESULTS AND DISCUSSION: The TMAs produced are of a high density (up to 104 cores each, 8×13) and allow a multiplex analysis of biomarkers in the context of clinical trials. BMJ Group 2010-11-15 2011-01 /pmc/articles/PMC3002837/ /pubmed/21081515 http://dx.doi.org/10.1136/jcp.2010.082339 Text en © 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Short Report
McCarthy, F
Dennis, N
Flohr, P
Jhavar, S
Parker, C
Cooper, C S
High-density tissue microarrays from prostate needle biopsies
title High-density tissue microarrays from prostate needle biopsies
title_full High-density tissue microarrays from prostate needle biopsies
title_fullStr High-density tissue microarrays from prostate needle biopsies
title_full_unstemmed High-density tissue microarrays from prostate needle biopsies
title_short High-density tissue microarrays from prostate needle biopsies
title_sort high-density tissue microarrays from prostate needle biopsies
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002837/
https://www.ncbi.nlm.nih.gov/pubmed/21081515
http://dx.doi.org/10.1136/jcp.2010.082339
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