Quantitative Analysis of Seven New Prostate Cancer Biomarkers and the Potential Future of the "Biomarker Laboratory'

被引:8
作者
Cao, Kevin [1 ]
Arthurs, Callum [1 ]
Atta-ul, Ali [2 ]
Millar, Michael [3 ]
Beltran, Mariana [4 ]
Neuhaus, Jochen [5 ]
Horn, Lars-Christian [6 ]
Henrique, Rui [7 ,8 ]
Ahmed, Aamir [1 ,2 ]
Thrasivoulou, Christopher [9 ]
机构
[1] Kings Coll London, Ctr Stem Cells & Regenerat Med, Prostate Canc Res Ctr, London WC2R 2LS, England
[2] UCL, Prostate Canc Res Ctr, London WC1E 6BT, England
[3] Univ Edinburgh, Queens Med Res Inst, Edinburgh EH8 9YL, Midlothian, Scotland
[4] Nine Edinburgh BioQuarter, Aquila BioMed, 9 Little France Rd, Edinburgh EH16 4UX, Midlothian, Scotland
[5] Univ Leipzig, Dept Urol, Res Lab, Urol Res Labs, Liebigstr 19,Bldg C, D-04103 Leipzig, Germany
[6] Univ Hosp Leipzig, Div Gynecol Breast & Perinatal Pathol, Liebigstasse 24 D, D-04103 Leipzig, Germany
[7] Portuguese Oncol Inst Porto, Dept Pathol, P-4200072 Porto, Portugal
[8] Univ Porto, Abel Salazar Inst Biomed Sci, Dept Pathol & Mol Immunol, P-4099002 Porto, Portugal
[9] UCL, Ctr Cell & Mol Dynam, Res Dept Cell & Dev Biol, Rockefeller Bldg, London WC1E 6BT, England
关键词
biomarker discovery; tissue microarray; automated workflow; clinical management; morphology-guided analysis; COA-BINDING PROTEIN; TISSUE MICROARRAYS; PROTEOMIC TECHNOLOGIES; EXPRESSION; CELLS; IDENTIFICATION; TRANSLATION; DISCOVERY; BREAST; GENE;
D O I
10.3390/diagnostics8030049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prostate cancer is the third highest cause of male mortality in the developed world, with the burden of the disease increasing dramatically with demographic change. There are significant limitations to the current diagnostic regimens and no established effective screening modality. To this end, research has discovered hundreds of potential biomarkers' that may one day be of use in screening, diagnosis or prognostication. However, the barriers to bringing biomarkers to clinical evaluation and eventually into clinical usage have yet to be realised. This is an operational challenge that requires some new thinking and development of paradigms to increase the efficiency of the laboratory process and add value' to the clinician. Value comes in various forms, whether it be a process that is seamlessly integrated into the hospital laboratory environment or one that can provide additional information' for the clinical pathologist in terms of risk profiling. We describe, herein, an efficient and tissue-conserving pipeline that uses Tissue Microarrays in a semi-automated process that could, one day, be integrated into the hospital laboratory domain, using seven putative prostate cancer biomarkers for illustration.
引用
收藏
页数:15
相关论文
共 79 条
[1]  
[Anonymous], 5 10 YEAR CANC PREV
[2]   Expression of ribosomal proteins in normal and cancerous human prostate tissue [J].
Arthurs, Callum ;
Murtaza, Bibi Nazia ;
Thomson, Calum ;
Dickens, Kerry ;
Henrique, Rui ;
Patel, Hitendra R. H. ;
Beltran, Mariana ;
Millar, Michael ;
Thrasivoulou, Christopher ;
Ahmed, Aamir .
PLOS ONE, 2017, 12 (10)
[3]   The ITM2B (BRI2) gene is a target of BCL6 repression: Implications for lymphomas and neurodegenerative diseases [J].
Baron, Beverly W. ;
Baron, Rebecca M. ;
Baron, Joseph M. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2015, 1852 (05) :742-748
[4]   Global cancer transitions according to the Human Development Index (2008-2030): a population-based study [J].
Bray, Freddie ;
Jemal, Ahmedin ;
Grey, Nathan ;
Ferlay, Jacques ;
Forman, David .
LANCET ONCOLOGY, 2012, 13 (08) :790-801
[5]   Evaluation of ERG and SPINK1 by Immunohistochemical Staining and Clinicopathological Outcomes in a Multi-Institutional Radical Prostatectomy Cohort of 1067 Patients [J].
Brooks, James D. ;
Wei, Wei ;
Hawley, Sarah ;
Auman, Heidi ;
Newcomb, Lisa ;
Boyer, Hilary ;
Fazli, Ladan ;
Simko, Jeff ;
Hurtado-Coll, Antonio ;
Troyer, Dean A. ;
Carroll, Peter R. ;
Gleave, Martin ;
Lance, Raymond ;
Lin, Daniel W. ;
Nelson, Peter S. ;
Thompson, Ian M. ;
True, Lawrence D. ;
Feng, Ziding ;
McKenney, Jesse K. .
PLOS ONE, 2015, 10 (07)
[6]   Systematic Analysis of the Expression of the Mitochondrial ATP Synthase (Complex V) Subunits in Clear Cell Renal Cell Carcinoma [J].
Brueggemann, Maria ;
Gromes, Arabella ;
Poss, Mirjam ;
Schmidt, Doris ;
Kuelmper, Niklas ;
Tolkach, Yuri ;
Dietrich, Dimo ;
Kristiansen, Glen ;
Mueller, Stefan C. ;
Ellinger, Joerg .
TRANSLATIONAL ONCOLOGY, 2017, 10 (04) :661-668
[7]   Immunohistochemical Expression of Hsp60 Correlates With Tumor Progression and Hormone Resistance in Prostate Cancer [J].
Castilla, Carolina ;
Congregado, Belen ;
Conde, Jose M. ;
Medina, Rafael ;
Torrubia, Francisco J. ;
Japon, Miguel A. ;
Saez, Carmen .
UROLOGY, 2010, 76 (04) :1017.e1-1017.e6
[8]  
Champy J., 1995, REENGINEERING CORPOR
[9]   ANALYSIS OF HEAT-SHOCK PROTEIN EXPRESSION IN MYELOID-LEUKEMIA CELLS BY FLOW-CYTOMETRY [J].
CHANT, ID ;
ROSE, PE ;
MORRIS, AG .
BRITISH JOURNAL OF HAEMATOLOGY, 1995, 90 (01) :163-168
[10]  
Chase R.B., 2005, OPERATIONS MANAGEMEN