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[利用表面增强激光解吸/电离飞行时间质谱建立结直肠癌预测模型]

[Establish predictive model of colorectal cancer by using surface enhanced laser desorption/ionization-time of flight-mass spectrometry].

作者信息

Lai Yan-Han, Xu Jian-Min, Yu Xin-Zhe, Zhong Yun-Shi, Wei Ye, Ren Li, Zhu De-Xiang, Liu Yin-Kun, Niu Wei-Xin, Qin Xin-Yu

机构信息

Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

出版信息

Zhonghua Wai Ke Za Zhi. 2008 Jul 1;46(13):995-7.

PMID:19035201
Abstract

OBJECTIVE

To establish serum proteome fingerprinting predictive models and search for proteins associated with colorectal cancer.

METHODS

Thirty-six randomly selected colorectal cancer patients and 36 cases with hernia or gall bladder diseases scheduled for elective operation were enrolled as cancer group and control group respectively. Peripheral venous blood samples were collected before the operations. Special serum protein or peptide fingerprint was investigated by using surface enhanced laser desorption/ ionization-time of flight-mass spectrometry (SELDI-TOF-MS) measurement after blood sample had been treated with weak cation exchange protein chip (CM10) for each case. The obtained data were analyzed by Biomarker Wizard software to screen serum proteome tumor markers and set up diagnosis predictive model for colorectal cancer. Blind validation of the model with 44 healthy controls and 88 colorectal cancer patients were carried out by using Biomarker Patterns Software.

RESULTS

In comparing colorectal cancer group with control group, 5 specific protein peaks (P < 0.05) were found. The predictive model had a sensitivity of 100% and a specificity of 97.2%. A sensitivity of 71.6% and a specificity of 72.7% was got with the blind validation. The specific protein peaks with a mass-to-charge ratio (m/z) of 8908 and 13,707 showed in all the results and it showed their strong relationship with colorectal cancer.

CONCLUSIONS

The predictive models built by the differences of serum proteome fingerprint could be a very useful diagnostic tool in colorectal cancer. Proteins with m/z of 8908 and 13,707 would possibly be the tumor markers of colorectal cancer.

摘要

目的

建立血清蛋白质组指纹图谱预测模型并寻找与结直肠癌相关的蛋白质。

方法

随机选取36例结直肠癌患者和36例计划择期手术的疝气或胆囊疾病患者,分别作为癌症组和对照组。术前采集外周静脉血样本。对每份血样用弱阳离子交换蛋白芯片(CM10)处理后,采用表面增强激光解吸/电离飞行时间质谱(SELDI-TOF-MS)检测特殊血清蛋白或肽指纹图谱。所得数据用Biomarker Wizard软件进行分析,以筛选血清蛋白质组肿瘤标志物并建立结直肠癌诊断预测模型。使用Biomarker Patterns软件对44名健康对照者和88例结直肠癌患者进行模型的盲法验证。

结果

结直肠癌组与对照组比较,发现5个特异性蛋白峰(P < 0.05)。预测模型的灵敏度为100%,特异度为97.2%。盲法验证的灵敏度为71.6%,特异度为72.7%。所有结果均显示质荷比(m/z)为8908和13707的特异性蛋白峰,表明它们与结直肠癌有密切关系。

结论

基于血清蛋白质组指纹图谱差异建立的预测模型可能是结直肠癌非常有用的诊断工具。质荷比为8908和13707的蛋白质可能是结直肠癌的肿瘤标志物。

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