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©2013 Baishideng Publishing Group Co.
World J Clin Urol. Nov 24, 2013; 2(3): 20-31
Published online Nov 24, 2013. doi: 10.5410/wjcu.v2.i3.20
Published online Nov 24, 2013. doi: 10.5410/wjcu.v2.i3.20
Biomarker/signature | Technology used | Ref. |
MCP-1 A2518G, SDF-1 3'A and chemokine receptors CCR2A V64I, CCR5 Δ32, CCR5 59029 and CXCR4 | PCR-restriction fragment length polymorphism | [21] |
TP53 | PCR-single strand conformational polymorphism analysis, DNA sequencing and immunohistochemical analysis | [22] |
H-ras gene mutations | COLD-PCR | [23] |
RARβ(2) and APC promoter methylation | Methylation specific PCR | [27] |
SCGB3A1, BNIP3, ID4 and RUNX3 | Multiplex ligation-dependent probe amplification | [28] |
TBX2, TBX3, GATA2 and ZIC4 | Genome-wide methylation analysis | [29] |
BCL2, CDKN2A and NID2 genes methylation | Nested methylation specific polymerase chain | [30] |
miR-96 and miR-183 | Q-PCR | [33] |
miR-618, miR-1255b-5p | RT-qPCR | [36] |
RNA ratio of v-ets erythroblastosis virus E26 oncogene homolog 2 (avian; ETS2) to urokinase plasminogen activator (uPA) | Reverse transcription quantitative-PCR | [41] |
HYAL1 and survivin RNA | Qualitative and semiquantitative reverse transcriptase-polymerase chain reaction | [42] |
FN, RTA, and CK20 | Detection of CK20 by conventional RT-PCR, estimation of fibronectin by ELISA and relative telomerase activity by TRAP | [46] |
CXCR4 and CXCR7 | qPCR and/or immunohistochemistry | [52] |
Bradeion/SEPT4 transcript | Real-time reverse transcriptase-polymerase chain reaction | [53] |
hTERT, SENP1, PPP1CA, and MCM5 mRNA | q-RT-PCR | [54] |
HOX-A13, IGBP-5, MDK, and CDC-2 | cDNA microarray, Q-PCR | [55,56] |
Afamin, adiponectin, complement C4 gamma chain, apolipoprotein A-II precursor, ceruloplasmin and prothrombin | iTRAQ | [61] |
IL-8, MMP-9, MMP-10, PAI-1, VEGF, ANG, CA9 and APOE | ELISA assay | [62] |
IL-8, MMP-9, MMP-10, SDC1, CCL18, PAI-1, CD44, VEGF, ANG, CA9, A1AT, OPN, PTX3 and APOE | ELISA assay | [63] |
GC | Two-dimensional fluorescent differential gel electrophoresis and MALDI-TOF/TOF MS | [64] |
beta-2-microglobulin, fatty acid-binding protein adipocyte, gelsolin, isoform 1 of gelsolin, myoglobin, isoform 2 of fibrinogen alpha chain, apoA-I, prostaglandin D(2) synthase 21 kDa, protein AMBP, transthyretin, keratin type II cytoskeletal 1, type II cytoskeletal 8, putative uncharacterized protein ALB, putative uncharacterized protein MASP2 (fragment) | 2-dimensional electrophoresis combined with MALDI-TOF/TOF MS and SWISS-PROT database | [65] |
MMP9, fibrinogen forms, and clusterin, aminopeptidase N, profilin 1 and myeloblastin | 1D-SDS-PAGE followed by band excision and liquid chromatography tandem MS | [66] |
Fibrinogen α chain precursor, apolipoprotein E, α-1-antitrypsin, and leucine-rich α-2-glycoprotein 1 | MS and western blot/dot blot | [67] |
Carnitine C9:1 and component I | Liquid chromatography-mass spectrometry based method | [72] |
Kynurenine | Two-dimensional gas chromatography time-of-flight mass spectrometry (GC×GC-TOFMS) | [73] |
HURP RNA | Conventional RT-PCR and AuNP nanoassay | [89] |
- Citation: Eissa S, Matboli M. Integrated technologies in the post-genomic era for discovery of bladder cancer urinary markers. World J Clin Urol 2013; 2(3): 20-31
- URL: https://www.wjgnet.com/2219-2816/full/v2/i3/20.htm
- DOI: https://dx.doi.org/10.5410/wjcu.v2.i3.20