Guidelines and considerations for conducting experiments using tissue microarrays

Tissue microarrays (TMAs) represent a powerful method for undertaking large‐scale tissue‐based biomarker studies. While TMAs offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA‐based research...

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Veröffentlicht in:Histopathology Jg. 62; H. 6; S. 827 - 839
Hauptverfasser: Ilyas, Mohammad, Grabsch, Heike, Ellis, Ian O, Womack, Chris, Brown, Robert, Berney, Dan, Fennell, Dean, Salto-Tellez, Manuel, Jenkins, Martin, Landberg, Goran, Byers, Richard, Treanor, Darren, Harrison, David, Green, Andrew R, Ball, Graham, Hamilton, Peter
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England Blackwell Publishing Ltd 01.05.2013
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ISSN:0309-0167, 1365-2559, 1365-2559
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Abstract Tissue microarrays (TMAs) represent a powerful method for undertaking large‐scale tissue‐based biomarker studies. While TMAs offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA‐based research, guidance on design and execution of experiments will be of benefit and should help researchers new to TMA‐based studies to avoid known pitfalls. Furthermore, a consensus on quality standards for TMA‐based experiments should improve the robustness and reproducibility of studies, thereby increasing the likelihood of identifying clinically useful biomarkers. In order to address these issues, the National Cancer Research Institute Biomarker and Imaging Clinical Studies Group organized a 1‐day TMA workshop held in Nottingham in May 2012. The document herein summarizes the conclusions from the workshop. It includes guidance and considerations on all aspects of TMA‐based research, including the pre‐analytical stages of experimental design, the analytical stages of data acquisition, and the postanalytical stages of data analysis. A checklist is presented which can be used both for planning a TMA experiment and interpreting the results of such an experiment. For studies of cancer biomarkers, this checklist could be used as a supplement to the REMARK guidelines.
AbstractList Tissue microarrays (TMAs) represent a powerful method for undertaking large‐scale tissue‐based biomarker studies. While TMAs offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA‐based research, guidance on design and execution of experiments will be of benefit and should help researchers new to TMA‐based studies to avoid known pitfalls. Furthermore, a consensus on quality standards for TMA‐based experiments should improve the robustness and reproducibility of studies, thereby increasing the likelihood of identifying clinically useful biomarkers. In order to address these issues, the National Cancer Research Institute Biomarker and Imaging Clinical Studies Group organized a 1‐day TMA workshop held in Nottingham in May 2012. The document herein summarizes the conclusions from the workshop. It includes guidance and considerations on all aspects of TMA‐based research, including the pre‐analytical stages of experimental design, the analytical stages of data acquisition, and the postanalytical stages of data analysis. A checklist is presented which can be used both for planning a TMA experiment and interpreting the results of such an experiment. For studies of cancer biomarkers, this checklist could be used as a supplement to the REMARK guidelines.
Tissue microarrays (TMAs) represent a powerful method for undertaking large-scale tissue-based biomarker studies. While TMAs offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA-based research, guidance on design and execution of experiments will be of benefit and should help researchers new to TMA-based studies to avoid known pitfalls. Furthermore, a consensus on quality standards for TMA-based experiments should improve the robustness and reproducibility of studies, thereby increasing the likelihood of identifying clinically useful biomarkers. In order to address these issues, the National Cancer Research Institute Biomarker and Imaging Clinical Studies Group organized a 1-day TMA workshop held in Nottingham in May 2012. The document herein summarizes the conclusions from the workshop. It includes guidance and considerations on all aspects of TMA-based research, including the pre-analytical stages of experimental design, the analytical stages of data acquisition, and the postanalytical stages of data analysis. A checklist is presented which can be used both for planning a TMA experiment and interpreting the results of such an experiment. For studies of cancer biomarkers, this checklist could be used as a supplement to the REMARK guidelines. [PUBLICATION ABSTRACT]
Tissue microarrays ( TMA s) represent a powerful method for undertaking large‐scale tissue‐based biomarker studies. While TMA s offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA ‐based research, guidance on design and execution of experiments will be of benefit and should help researchers new to TMA ‐based studies to avoid known pitfalls. Furthermore, a consensus on quality standards for TMA ‐based experiments should improve the robustness and reproducibility of studies, thereby increasing the likelihood of identifying clinically useful biomarkers. In order to address these issues, the N ational C ancer R esearch I nstitute B iomarker and I maging C linical S tudies G roup organized a 1‐day TMA workshop held in N ottingham in M ay 2012. The document herein summarizes the conclusions from the workshop. It includes guidance and considerations on all aspects of TMA ‐based research, including the pre‐analytical stages of experimental design, the analytical stages of data acquisition, and the postanalytical stages of data analysis. A checklist is presented which can be used both for planning a TMA experiment and interpreting the results of such an experiment. For studies of cancer biomarkers, this checklist could be used as a supplement to the REMARK guidelines.
Tissue microarrays (TMAs) represent a powerful method for undertaking large-scale tissue-based biomarker studies. While TMAs offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA-based research, guidance on design and execution of experiments will be of benefit and should help researchers new to TMA-based studies to avoid known pitfalls. Furthermore, a consensus on quality standards for TMA-based experiments should improve the robustness and reproducibility of studies, thereby increasing the likelihood of identifying clinically useful biomarkers. In order to address these issues, the National Cancer Research Institute Biomarker and Imaging Clinical Studies Group organized a 1-day TMA workshop held in Nottingham in May 2012. The document herein summarizes the conclusions from the workshop. It includes guidance and considerations on all aspects of TMA-based research, including the pre-analytical stages of experimental design, the analytical stages of data acquisition, and the postanalytical stages of data analysis. A checklist is presented which can be used both for planning a TMA experiment and interpreting the results of such an experiment. For studies of cancer biomarkers, this checklist could be used as a supplement to the REMARK guidelines.Tissue microarrays (TMAs) represent a powerful method for undertaking large-scale tissue-based biomarker studies. While TMAs offer several advantages, there are a number of issues specific to their use which need to be considered when employing this method. Given the investment in TMA-based research, guidance on design and execution of experiments will be of benefit and should help researchers new to TMA-based studies to avoid known pitfalls. Furthermore, a consensus on quality standards for TMA-based experiments should improve the robustness and reproducibility of studies, thereby increasing the likelihood of identifying clinically useful biomarkers. In order to address these issues, the National Cancer Research Institute Biomarker and Imaging Clinical Studies Group organized a 1-day TMA workshop held in Nottingham in May 2012. The document herein summarizes the conclusions from the workshop. It includes guidance and considerations on all aspects of TMA-based research, including the pre-analytical stages of experimental design, the analytical stages of data acquisition, and the postanalytical stages of data analysis. A checklist is presented which can be used both for planning a TMA experiment and interpreting the results of such an experiment. For studies of cancer biomarkers, this checklist could be used as a supplement to the REMARK guidelines.
Author Ilyas, Mohammad
Landberg, Goran
Jenkins, Martin
Brown, Robert
Hamilton, Peter
Womack, Chris
Salto-Tellez, Manuel
Ellis, Ian O
Byers, Richard
Ball, Graham
Treanor, Darren
Green, Andrew R
Harrison, David
Grabsch, Heike
Fennell, Dean
Berney, Dan
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  surname: Ilyas
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  email: mohammad.ilyas@nottingham.ac.uk
  organization: School of Molecular Medical Sciences, Queen's Medical Centre, Nottingham University, Nottingham, UK
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  surname: Grabsch
  fullname: Grabsch, Heike
  organization: Section of Pathology and Tumour Biology, Leeds Institute of Molecular Medicine, St James's University Hospital, Leeds, UK
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  givenname: Ian O
  surname: Ellis
  fullname: Ellis, Ian O
  organization: School of Molecular Medical Sciences, Queen's Medical Centre, Nottingham University, Nottingham, UK
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  givenname: Chris
  surname: Womack
  fullname: Womack, Chris
  organization: Department of Histopathology, Manchester Royal Infirmary, Manchester, UK
– sequence: 5
  givenname: Robert
  surname: Brown
  fullname: Brown, Robert
  organization: Hammersmith Hospital, Epigenetics Unit, 4th Floor IRDB, London, UK
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  surname: Berney
  fullname: Berney, Dan
  organization: Department of Pathology, Barts and The London School of Medicine and Dentistry, London, UK
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  givenname: Dean
  surname: Fennell
  fullname: Fennell, Dean
  organization: University of Leicester and Leicester University Hospitals, Leicester, UK
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  surname: Salto-Tellez
  fullname: Salto-Tellez, Manuel
  organization: Centre for Cancer Research and Cell Biology, University Road, Belfast, UK
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  givenname: Martin
  surname: Jenkins
  fullname: Jenkins, Martin
  organization: AstraZeneca Oncology Innovative Medicines, Cheshire, Macclesfield, UK
– sequence: 10
  givenname: Goran
  surname: Landberg
  fullname: Landberg, Goran
  organization: Department of Histopathology, Manchester Royal Infirmary, Manchester, UK
– sequence: 11
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  surname: Byers
  fullname: Byers, Richard
  organization: Department of Histopathology, Manchester Royal Infirmary, Manchester, UK
– sequence: 12
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  surname: Treanor
  fullname: Treanor, Darren
  organization: St James University Hospital, Leeds Institute of Molecular Medicine, Leeds, UK
– sequence: 13
  givenname: David
  surname: Harrison
  fullname: Harrison, David
  organization: School of Medicine, University of St Andrews, St Andrews, Fife, UK
– sequence: 14
  givenname: Andrew R
  surname: Green
  fullname: Green, Andrew R
  organization: Department of Histopathology, Manchester Royal Infirmary, Manchester, UK
– sequence: 15
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  surname: Ball
  fullname: Ball, Graham
  organization: John Van Geest Cancer Research Centre, School of Science and Technology, Nottingham Trent University, Nottingham, UK
– sequence: 16
  givenname: Peter
  surname: Hamilton
  fullname: Hamilton, Peter
  organization: PathXL Ltd, Northern Ireland Science Park, Belfast, UK
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23672312$$D View this record in MEDLINE/PubMed
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2013 Blackwell Publishing Ltd.
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References Elsheikh SE, Green AR, Rakha EA et al. Global histone modifications in breast cancer correlate with tumor phenotypes, prognostic factors, and patient outcome. Cancer Res. 2009; 69; 3802-3809.
McCabe A, Dolled-Filhart M, Camp RL et al. Automated quantitative analysis (AQUA) of in situ protein expression, antibody concentration, and prognosis. J. Natl Cancer Inst. 2005; 97; 1808-1815.
Jenkins M, Flynn A, Smart T et al. A statistician's perspective on biomarkers in drug development. Pharm. Stat. 2011; 10; 494-507.
Zhang D, Salto-Tellez M, Putti TC et al. Reliability of tissue microarrays in detecting protein expression and gene amplification in breast cancer. Mod. Pathol. 2003; 16; 79-84.
Walker RA. Quantification of immunohistochemistry - issues concerning methods, utility and semiquantitative assessment I. Histopathology 2006; 49; 406-410.
Wan WH, Fortuna MB, Furmanski P. A rapid and efficient method for testing immunohistochemical reactivity of monoclonal antibodies against multiple tissue samples simultaneously. J. Immunol. Methods 1987; 103; 121-129.
Dennis J, Westra J, Bell A et al. The type and quality of paraffin wax is important when constructing tissue microarrays. Mol. Pathol. 2003; 56; 306.
Okunieff P, Hoeckel M, Dunphy EP et al. Oxygen tension distributions are sufficient to explain the local response of human breast tumors treated with radiation alone. Int. J. Radiat. Oncol. Biol. Phys. 1993; 26; 631-636.
Hoos A, Cordon-Cardo C. Tissue microarray profiling of cancer specimens and cell lines: opportunities and limitations. Lab. Invest. 2001; 81; 1331-1338.
Schmidt LH, Biesterfeld S, Kummel A et al. Tissue microarrays are reliable tools for the clinicopathological characterization of lung cancer tissue. Anticancer Res. 2009; 29; 201-209.
Schlomm T, Nakel E, Lubke A et al. Marked gene transcript level alterations occur early during radical prostatectomy. Eur. Urol. 2008; 53; 333-344.
Ong CW, Kim LG, Kong HH et al. Computer-assisted pathological immunohistochemistry scoring is more time-effective than conventional scoring, but provides no analytical advantage. Histopathology 2010; 56; 523-529.
Bubendorf L, Kononen J, Koivisto P et al. Survey of gene amplifications during prostate cancer progression by high-throughout fluorescence in situ hybridization on tissue microarrays. Cancer Res. 1999; 59; 803-806.
Kononen J, Bubendorf L, Kallioniemi A et al. Tissue microarrays for high-throughput molecular profiling of tumor specimens. Nat. Med. 1998; 4; 844-847.
Das K, Mohd Omar MF, Ong CW et al. TRARESA: a tissue microarray-based hospital system for biomarker validation and discovery. Pathology 2008; 40; 441-449.
Jubb AM, Pham TQ, Hanby AM et al. Expression of vascular endothelial growth factor, hypoxia inducible factor 1alpha, and carbonic anhydrase IX in human tumours. J. Clin. Pathol. 2004; 57; 504-512.
Goethals L, Perneel C, Debucquoy A et al. A new approach to the validation of tissue microarrays. J. Pathol. 2006; 208; 607-614.
Rubin MA, Dunn R, Strawderman M et al. Tissue microarray sampling strategy for prostate cancer biomarker analysis. Am. J. Surg. Pathol. 2002; 26; 312-319.
Montgomery K, Zhao S, van de Rijn M et al. A novel method for making 'tissue' microarrays from small numbers of suspension cells. Appl. Immunohistochem. Mol. Morphol. 2005; 13; 80-84.
Catchpoole D, Mackie N, McIver S et al. Tape transfer sectioning of tissue microarrays introduces nonspecific immunohistochemical staining artifacts. Biotech. Histochem. 2010; 86; 421-428.
Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986; 1; 307-310.
Wampfler JA, Aubry MC, Riehle DL et al. Determining the optimal numbers of cores based on tissue microarray antibody assessment in non-small cell lung cancer. J. Cancer Sci. Ther. 2011; 3; 120-124.
Camp RL, Charette LA, Rimm DL. Validation of tissue microarray technology in breast carcinoma. Lab. Invest. 2000; 80; 1943-1949.
Altman DG, McShane LM, Sauerbrei W et al. Reporting recommendations for tumor marker prognostic studies (REMARK): explanation and elaboration. BMC Med. 2012; 10; 51.
Battifora H. The multitumor (sausage) tissue block: novel method for immunohistochemical antibody testing. Lab. Invest. 1986; 55; 244-248.
Berman JJ, Datta M, Kajdacsy-Balla A et al. The tissue microarray data exchange specification: implementation by the Cooperative Prostate Cancer Tissue Resource. BMC Bioinformatics 2004; 5; 19.
Anagnostou VK, Lowery FJ, Syrigos KN et al. Quantitative evaluation of protein expression as a function of tissue microarray core diameter: is a large (1.5 mm) core better than a small (0.6 mm) core? Arch. Pathol. Lab. Med. 2010; 134; 613-619.
Goranova TE, Ohue M, Shimoharu Y et al. Dynamics of cancer cell subpopulations in primary and metastatic colorectal tumors. Clin. Exp. Metastasis 2011; 28; 427-435.
Li H, Sun Y, Kong QY et al. Combination of nucleic acid and protein isolation with tissue array construction: using defined histologic regions in single frozen tissue blocks for multiple research purposes. Int. J. Mol. Med. 2003; 12; 299-304.
McShane LM, Altman DG, Sauerbrei W et al. REporting recommendations for tumour MARKer prognostic studies (REMARK). Br. J. Cancer 2005; 93; 387-391.
Bortoletto G, Campagnolo D, Mirandola S et al. Comparable performance of TMA and real-time PCR in detecting minimal residual hepatitis C viraemia at the end of antiviral therapy. J. Clin. Virol. 2011; 50; 217-220.
Yan P, Seelentag W, Bachmann A et al. An agarose matrix facilitates sectioning of tissue microarray blocks. J. Histochem. Cytochem. 2007; 55; 21-24.
Waterworth A, Hanby A, Speirs V. A novel cell array technique for high-throughput, cell-based analysis. In Vitro Cell. Dev. Biol. Anim. 2005; 41; 185-187.
LeBaron MJ, Crismon HR, Utama FE et al. Ultrahigh density microarrays of solid samples. Nat. Methods 2005; 2; 511-513.
Betsou F, Barnes R, Burke T et al. Human biospecimen research: experimental protocol and quality control tools. Cancer Epidemiol. Biomark. Prev. 2009; 18; 1017-1025.
Wright A, Lyttleton O, Lewis P et al. The tissue microarray data exchange specification: extending TMA DES to provide flexible scoring and incorporate virtual slides. J. Pathol. Inform. 2011; 2; 15.
DiVito KA, Charette LA, Rimm DL et al. Long-term preservation of antigenicity on tissue microarrays. Lab. Invest. 2004; 84; 1071-1078.
Anagnostou VK, Welsh AW, Giltnane JM et al. Analytic variability in immunohistochemistry biomarker studies. Cancer Epidemiol. Biomark. Prev. 2010; 19; 982-991.
Fadhil W, Ilyas M. Immunostaining for mismatch repair (MMR) protein expression in colorectal cancer is better and easier to interpret when performed on diagnostic biopsies. Histopathology 2012; 60; 653-655.
Pintilie M, Iakovlev V, Fyles A et al. Heterogeneity and power in clinical biomarker studies. J. Clin. Oncol. 2009; 27; 1517-1521.
Bova GS, Parmigiani G, Epstein JI et al. Web-based tissue microarray image data analysis: initial validation testing through prostate cancer Gleason grading. Hum. Pathol. 2001; 32; 417-427.
Berman JJ, Edgerton ME, Friedman BA. The tissue microarray data exchange specification: a community-based, open source tool for sharing tissue microarray data. BMC Med. Inform. Decis. Mak. 2003; 3; 5.
Nocito A, Kononen J, Kallioniemi OP et al. Tissue microarrays (TMAs) for high-throughput molecular pathology research. Int. J. Cancer 2001; 94; 1-5.
Sharma-Oates A, Quirke P, Westhead DR. TmaDB: a repository for tissue microarray data. BMC Bioinformatics 2005; 6; 218.
Datta MW, Kahler A, Macias V et al. A simple inexpensive method for the production of tissue microarrays from needle biopsy specimens: examples with prostate cancer. Appl. Immunohistochem. Mol. Morphol. 2005; 13; 96-103.
Abd El-Rehim DM, Ball G, Pinder SE et al. High-throughput protein expression analysis using tissue microarray technology of a large well-characterised series identifies biologically distinct classes of breast cancer confirming recent cDNA expression analyses. Int. J. Cancer 2005; 116; 340-350.
Bentzen SM, Buffa FM, Wilson GD. Multiple biomarker tissue microarrays: bioinformatics and practical approaches. Cancer Metastasis Rev. 2008; 27; 481-494.
Taylor CR, Levenson RM. Quantification of immunohistochemistry - issues concerning methods, utility and semiquantitative assessment II. Histopathology 2006; 49; 411-424.
Huang J, Qi R, Quackenbush J et al. Effects of ischemia on gene expression. J. Surg. Res. 2001; 99; 222-227.
1993; 26
2010; 56
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2001; 94
2004; 84
2011; 2
2010; 19
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1986; 55
2005; 116
2005; 41
2011; 10
2003; 16
2004; 5
2008; 53
2011; 3
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2009; 27
2012; 10
2009; 29
2003; 12
2003; 56
2001; 81
1986; 1
2002; 26
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2006; 208
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1999; 59
2008; 27
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2011; 50
2003; 3
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References_xml – reference: Catchpoole D, Mackie N, McIver S et al. Tape transfer sectioning of tissue microarrays introduces nonspecific immunohistochemical staining artifacts. Biotech. Histochem. 2010; 86; 421-428.
– reference: Walker RA. Quantification of immunohistochemistry - issues concerning methods, utility and semiquantitative assessment I. Histopathology 2006; 49; 406-410.
– reference: Das K, Mohd Omar MF, Ong CW et al. TRARESA: a tissue microarray-based hospital system for biomarker validation and discovery. Pathology 2008; 40; 441-449.
– reference: Yan P, Seelentag W, Bachmann A et al. An agarose matrix facilitates sectioning of tissue microarray blocks. J. Histochem. Cytochem. 2007; 55; 21-24.
– reference: Abd El-Rehim DM, Ball G, Pinder SE et al. High-throughput protein expression analysis using tissue microarray technology of a large well-characterised series identifies biologically distinct classes of breast cancer confirming recent cDNA expression analyses. Int. J. Cancer 2005; 116; 340-350.
– reference: Schlomm T, Nakel E, Lubke A et al. Marked gene transcript level alterations occur early during radical prostatectomy. Eur. Urol. 2008; 53; 333-344.
– reference: Goethals L, Perneel C, Debucquoy A et al. A new approach to the validation of tissue microarrays. J. Pathol. 2006; 208; 607-614.
– reference: Jubb AM, Pham TQ, Hanby AM et al. Expression of vascular endothelial growth factor, hypoxia inducible factor 1alpha, and carbonic anhydrase IX in human tumours. J. Clin. Pathol. 2004; 57; 504-512.
– reference: Nocito A, Kononen J, Kallioniemi OP et al. Tissue microarrays (TMAs) for high-throughput molecular pathology research. Int. J. Cancer 2001; 94; 1-5.
– reference: Dennis J, Westra J, Bell A et al. The type and quality of paraffin wax is important when constructing tissue microarrays. Mol. Pathol. 2003; 56; 306.
– reference: Waterworth A, Hanby A, Speirs V. A novel cell array technique for high-throughput, cell-based analysis. In Vitro Cell. Dev. Biol. Anim. 2005; 41; 185-187.
– reference: Bubendorf L, Kononen J, Koivisto P et al. Survey of gene amplifications during prostate cancer progression by high-throughout fluorescence in situ hybridization on tissue microarrays. Cancer Res. 1999; 59; 803-806.
– reference: Jenkins M, Flynn A, Smart T et al. A statistician's perspective on biomarkers in drug development. Pharm. Stat. 2011; 10; 494-507.
– reference: Huang J, Qi R, Quackenbush J et al. Effects of ischemia on gene expression. J. Surg. Res. 2001; 99; 222-227.
– reference: Camp RL, Charette LA, Rimm DL. Validation of tissue microarray technology in breast carcinoma. Lab. Invest. 2000; 80; 1943-1949.
– reference: Goranova TE, Ohue M, Shimoharu Y et al. Dynamics of cancer cell subpopulations in primary and metastatic colorectal tumors. Clin. Exp. Metastasis 2011; 28; 427-435.
– reference: Wright A, Lyttleton O, Lewis P et al. The tissue microarray data exchange specification: extending TMA DES to provide flexible scoring and incorporate virtual slides. J. Pathol. Inform. 2011; 2; 15.
– reference: Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986; 1; 307-310.
– reference: Altman DG, McShane LM, Sauerbrei W et al. Reporting recommendations for tumor marker prognostic studies (REMARK): explanation and elaboration. BMC Med. 2012; 10; 51.
– reference: Bortoletto G, Campagnolo D, Mirandola S et al. Comparable performance of TMA and real-time PCR in detecting minimal residual hepatitis C viraemia at the end of antiviral therapy. J. Clin. Virol. 2011; 50; 217-220.
– reference: Wampfler JA, Aubry MC, Riehle DL et al. Determining the optimal numbers of cores based on tissue microarray antibody assessment in non-small cell lung cancer. J. Cancer Sci. Ther. 2011; 3; 120-124.
– reference: Kononen J, Bubendorf L, Kallioniemi A et al. Tissue microarrays for high-throughput molecular profiling of tumor specimens. Nat. Med. 1998; 4; 844-847.
– reference: Hoos A, Cordon-Cardo C. Tissue microarray profiling of cancer specimens and cell lines: opportunities and limitations. Lab. Invest. 2001; 81; 1331-1338.
– reference: Ong CW, Kim LG, Kong HH et al. Computer-assisted pathological immunohistochemistry scoring is more time-effective than conventional scoring, but provides no analytical advantage. Histopathology 2010; 56; 523-529.
– reference: Zhang D, Salto-Tellez M, Putti TC et al. Reliability of tissue microarrays in detecting protein expression and gene amplification in breast cancer. Mod. Pathol. 2003; 16; 79-84.
– reference: Bentzen SM, Buffa FM, Wilson GD. Multiple biomarker tissue microarrays: bioinformatics and practical approaches. Cancer Metastasis Rev. 2008; 27; 481-494.
– reference: Battifora H. The multitumor (sausage) tissue block: novel method for immunohistochemical antibody testing. Lab. Invest. 1986; 55; 244-248.
– reference: Sharma-Oates A, Quirke P, Westhead DR. TmaDB: a repository for tissue microarray data. BMC Bioinformatics 2005; 6; 218.
– reference: Berman JJ, Datta M, Kajdacsy-Balla A et al. The tissue microarray data exchange specification: implementation by the Cooperative Prostate Cancer Tissue Resource. BMC Bioinformatics 2004; 5; 19.
– reference: Montgomery K, Zhao S, van de Rijn M et al. A novel method for making 'tissue' microarrays from small numbers of suspension cells. Appl. Immunohistochem. Mol. Morphol. 2005; 13; 80-84.
– reference: Anagnostou VK, Welsh AW, Giltnane JM et al. Analytic variability in immunohistochemistry biomarker studies. Cancer Epidemiol. Biomark. Prev. 2010; 19; 982-991.
– reference: Anagnostou VK, Lowery FJ, Syrigos KN et al. Quantitative evaluation of protein expression as a function of tissue microarray core diameter: is a large (1.5 mm) core better than a small (0.6 mm) core? Arch. Pathol. Lab. Med. 2010; 134; 613-619.
– reference: Taylor CR, Levenson RM. Quantification of immunohistochemistry - issues concerning methods, utility and semiquantitative assessment II. Histopathology 2006; 49; 411-424.
– reference: Elsheikh SE, Green AR, Rakha EA et al. Global histone modifications in breast cancer correlate with tumor phenotypes, prognostic factors, and patient outcome. Cancer Res. 2009; 69; 3802-3809.
– reference: Datta MW, Kahler A, Macias V et al. A simple inexpensive method for the production of tissue microarrays from needle biopsy specimens: examples with prostate cancer. Appl. Immunohistochem. Mol. Morphol. 2005; 13; 96-103.
– reference: Fadhil W, Ilyas M. Immunostaining for mismatch repair (MMR) protein expression in colorectal cancer is better and easier to interpret when performed on diagnostic biopsies. Histopathology 2012; 60; 653-655.
– reference: McShane LM, Altman DG, Sauerbrei W et al. REporting recommendations for tumour MARKer prognostic studies (REMARK). Br. J. Cancer 2005; 93; 387-391.
– reference: Berman JJ, Edgerton ME, Friedman BA. The tissue microarray data exchange specification: a community-based, open source tool for sharing tissue microarray data. BMC Med. Inform. Decis. Mak. 2003; 3; 5.
– reference: McCabe A, Dolled-Filhart M, Camp RL et al. Automated quantitative analysis (AQUA) of in situ protein expression, antibody concentration, and prognosis. J. Natl Cancer Inst. 2005; 97; 1808-1815.
– reference: Okunieff P, Hoeckel M, Dunphy EP et al. Oxygen tension distributions are sufficient to explain the local response of human breast tumors treated with radiation alone. Int. J. Radiat. Oncol. Biol. Phys. 1993; 26; 631-636.
– reference: DiVito KA, Charette LA, Rimm DL et al. Long-term preservation of antigenicity on tissue microarrays. Lab. Invest. 2004; 84; 1071-1078.
– reference: Schmidt LH, Biesterfeld S, Kummel A et al. Tissue microarrays are reliable tools for the clinicopathological characterization of lung cancer tissue. Anticancer Res. 2009; 29; 201-209.
– reference: Li H, Sun Y, Kong QY et al. Combination of nucleic acid and protein isolation with tissue array construction: using defined histologic regions in single frozen tissue blocks for multiple research purposes. Int. J. Mol. Med. 2003; 12; 299-304.
– reference: LeBaron MJ, Crismon HR, Utama FE et al. Ultrahigh density microarrays of solid samples. Nat. Methods 2005; 2; 511-513.
– reference: Bova GS, Parmigiani G, Epstein JI et al. Web-based tissue microarray image data analysis: initial validation testing through prostate cancer Gleason grading. Hum. Pathol. 2001; 32; 417-427.
– reference: Pintilie M, Iakovlev V, Fyles A et al. Heterogeneity and power in clinical biomarker studies. J. Clin. Oncol. 2009; 27; 1517-1521.
– reference: Wan WH, Fortuna MB, Furmanski P. A rapid and efficient method for testing immunohistochemical reactivity of monoclonal antibodies against multiple tissue samples simultaneously. J. Immunol. Methods 1987; 103; 121-129.
– reference: Rubin MA, Dunn R, Strawderman M et al. Tissue microarray sampling strategy for prostate cancer biomarker analysis. Am. J. Surg. Pathol. 2002; 26; 312-319.
– reference: Betsou F, Barnes R, Burke T et al. Human biospecimen research: experimental protocol and quality control tools. Cancer Epidemiol. Biomark. Prev. 2009; 18; 1017-1025.
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  year: 2004
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  publication-title: BMC Bioinformatics
– volume: 4
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  article-title: Tissue microarrays for high‐throughput molecular profiling of tumor specimens
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  year: 2011
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  article-title: Comparable performance of TMA and real‐time PCR in detecting minimal residual hepatitis C viraemia at the end of antiviral therapy
  publication-title: J. Clin. Virol.
– volume: 29
  start-page: 201
  year: 2009
  end-page: 209
  article-title: Tissue microarrays are reliable tools for the clinicopathological characterization of lung cancer tissue
  publication-title: Anticancer Res.
– volume: 116
  start-page: 340
  year: 2005
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  article-title: High‐throughput protein expression analysis using tissue microarray technology of a large well‐characterised series identifies biologically distinct classes of breast cancer confirming recent cDNA expression analyses
  publication-title: Int. J. Cancer
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  article-title: Validation of tissue microarray technology in breast carcinoma
  publication-title: Lab. Invest.
– volume: 55
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  end-page: 248
  article-title: The multitumor (sausage) tissue block: novel method for immunohistochemical antibody testing
  publication-title: Lab. Invest.
– volume: 6
  start-page: 218
  year: 2005
  article-title: TmaDB: a repository for tissue microarray data
  publication-title: BMC Bioinformatics
– volume: 26
  start-page: 312
  year: 2002
  end-page: 319
  article-title: Tissue microarray sampling strategy for prostate cancer biomarker analysis
  publication-title: Am. J. Surg. Pathol.
– volume: 93
  start-page: 387
  year: 2005
  end-page: 391
  article-title: REporting recommendations for tumour MARKer prognostic studies (REMARK)
  publication-title: Br. J. Cancer
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  article-title: A rapid and efficient method for testing immunohistochemical reactivity of monoclonal antibodies against multiple tissue samples simultaneously
  publication-title: J. Immunol. Methods
– volume: 10
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  year: 2011
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  article-title: A statistician's perspective on biomarkers in drug development
  publication-title: Pharm. Stat.
– volume: 28
  start-page: 427
  year: 2011
  end-page: 435
  article-title: Dynamics of cancer cell subpopulations in primary and metastatic colorectal tumors
  publication-title: Clin. Exp. Metastasis
– volume: 19
  start-page: 982
  year: 2010
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  article-title: Analytic variability in immunohistochemistry biomarker studies
  publication-title: Cancer Epidemiol. Biomark. Prev.
– volume: 27
  start-page: 1517
  year: 2009
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  article-title: Heterogeneity and power in clinical biomarker studies
  publication-title: J. Clin. Oncol.
– volume: 84
  start-page: 1071
  year: 2004
  end-page: 1078
  article-title: Long‐term preservation of antigenicity on tissue microarrays
  publication-title: Lab. Invest.
– volume: 134
  start-page: 613
  year: 2010
  end-page: 619
  article-title: Quantitative evaluation of protein expression as a function of tissue microarray core diameter: is a large (1.5 mm) core better than a small (0.6 mm) core?
  publication-title: Arch. Pathol. Lab. Med.
– volume: 53
  start-page: 333
  year: 2008
  end-page: 344
  article-title: Marked gene transcript level alterations occur early during radical prostatectomy
  publication-title: Eur. Urol.
– volume: 57
  start-page: 504
  year: 2004
  end-page: 512
  article-title: Expression of vascular endothelial growth factor, hypoxia inducible factor 1alpha, and carbonic anhydrase IX in human tumours
  publication-title: J. Clin. Pathol.
– volume: 2
  start-page: 15
  year: 2011
  article-title: The tissue microarray data exchange specification: extending TMA DES to provide flexible scoring and incorporate virtual slides
  publication-title: J. Pathol. Inform.
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  publication-title: Biotech. Histochem.
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  year: 2006
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  article-title: A new approach to the validation of tissue microarrays
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– volume: 27
  start-page: 481
  year: 2008
  end-page: 494
  article-title: Multiple biomarker tissue microarrays: bioinformatics and practical approaches
  publication-title: Cancer Metastasis Rev.
– volume: 60
  start-page: 653
  year: 2012
  end-page: 655
  article-title: Immunostaining for mismatch repair (MMR) protein expression in colorectal cancer is better and easier to interpret when performed on diagnostic biopsies
  publication-title: Histopathology
– volume: 10
  start-page: 51
  year: 2012
  article-title: Reporting recommendations for tumor marker prognostic studies (REMARK): explanation and elaboration
  publication-title: BMC Med.
– volume: 49
  start-page: 406
  year: 2006
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  article-title: Quantification of immunohistochemistry – issues concerning methods, utility and semiquantitative assessment I
  publication-title: Histopathology
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  year: 2003
  end-page: 304
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  publication-title: Int. J. Mol. Med.
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  article-title: Effects of ischemia on gene expression
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Snippet Tissue microarrays (TMAs) represent a powerful method for undertaking large‐scale tissue‐based biomarker studies. While TMAs offer several advantages, there...
Tissue microarrays ( TMA s) represent a powerful method for undertaking large‐scale tissue‐based biomarker studies. While TMA s offer several advantages, there...
Tissue microarrays (TMAs) represent a powerful method for undertaking large-scale tissue-based biomarker studies. While TMAs offer several advantages, there...
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SubjectTerms Academies and Institutes
Biomarkers
Biomarkers - metabolism
data interpretation
Data Interpretation, Statistical
experimental design
Experiments
guidance
Humans
Immunohistochemistry
Medical research
Quality Control
Studies
Tissue Array Analysis - methods
Tissue Array Analysis - standards
Tissue Array Analysis - statistics & numerical data
tissue microarray
United Kingdom
Title Guidelines and considerations for conducting experiments using tissue microarrays
URI https://api.istex.fr/ark:/67375/WNG-71BSPRQB-D/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fhis.12118
https://www.ncbi.nlm.nih.gov/pubmed/23672312
https://www.proquest.com/docview/1338444975
https://www.proquest.com/docview/1352280497
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