Differential expression of proteomics models of colorectal cancer, colorectal benign disease and healthy controls.
Differential expression of proteomics models of colorectal cancer, colorectal benign disease and healthy controls.
复制标题
结直肠癌、结直肠良性疾病和健康对照蛋白质组学模型的差异表达
DOI:
10.1186/1477-5956-8-16
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发表时间:
2010-03-25
期刊:
影响因子:
2
通讯作者:
Liu JR
中科院分区:
文献类型:
--
作者:
Liu M;Li CF;Chen HS;Lin LQ;Zhang CP;Zhao JL;Liu Y;Zhang SJ;Jin JC;Wang L;Liu JR
BackgroundColorectal cancer (CRC) is often diagnosed at a late stage with concomitant poor prognosis. The hypersensitive analytical technique of proteomics can detect molecular changes before the tumor is palpable. The surface-enhanced laser desorption/ionization-time of flight-mass spectra (SELDI-TOF-MS) is a newly-developed technique of evaluating protein separation in recent years. The protein chips have established the expression of tumor protein in the serum specimens and become the newly discovered markers for tumor diagnosis. The objective of this study was to find new markers of the diagnosis among groups of CRC, colorectal benign diseases (CBD) and healthy controls. The assay of SELDI-TOF-MS with analytical technique of protein-chip bioinformatics was used to detect the expression of protein mass peaks in the sera of patients or controls. One hundred serum samples, including 52 cases of colorectal cancer, 27 cases of colorectal benign disease, and 21 cases of healthy controls, were examined by SELDI-TOF-MS with WCX2 protein-chips.ResultsThe diagnostic models (I, II and III) were setup by analyzed the data and sieved markers using Ciphergen - Protein-Chip-Software 5.1. These models were combined with 3 protein mass peaks to discriminate CRC, CBD, and healthy controls. The accuracy, the sensitivity and the particularity of cross verification of these models are all highly over 80%.ConclusionsThe SELDI-TOF-MS is a useful tool to help diagnose colorectal cancer, especially during the early stage. However, identification of the significantly differentiated proteins needs further study.
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