期刊文献+

血清蛋白质指纹图谱对晚期结直肠癌一线化疗效果的预测作用

Research on the biomarkers for the prediction of efficacy in first-line chemotherapy of metastatic colorectal cancer using SELDI-TOF-MS
原文传递
导出
摘要 目的寻找能预测晚期结直肠癌一线化疗疗效的血清蛋白标记物。方法选择2008年8月至2010年7月在浙江大学医学院附属第二医院的70例从未接受过治疗的晚期结直肠癌患者,其中44例患者接受FOLFOX方案化疗,26例患者接受FOLFIRI方案化疗,进行4个疗程治疗后使用RECIST评价标准区分化疗受益者(R)和化疗无效者(NR)。留取化疗前患者血清标本,采用SELDI-TOF-MS和人工神经网络对一线化疗的疗效进行预测分析。结果根据RECIST标准,42例患者为化疗受益者,28例患者为化疗无效者,分析两组患者血清蛋白质指纹图谱的差异,筛选出10个蛋白质峰在化疗受益组的表达明显高于化疗无效组;并由这10个峰构建出结直肠癌一线化疗疗效的预测模型。经交叉验证,该模型的总准确率为90.0%(63/70)。结论蛋白质指纹图谱模型是预测晚期结直肠癌患者一线化疗方案治疗效果的有效方法之一。 Objective To identify serum protein patterns which could predict the efficacy of firstline chemotherapy of metastatic colorectal cancer ( CRC ). Methods Serum from 70 patients diagnosed as metastatic colorectal cancer before first-line chemotherapy were collected and analyzed for protein patterns using ANN analysis of SELDI-TOF-MS. Among the 70 cases, 44 patients received FOLFOX regimen, while the other 26 patients received FOLFIRI regimen. After four cycles of the treatment, RECIST criteria were used to define the responders (R) and non-responders (NR). Results With the method of SELDI-TOF-MS, 10 protein peaks were identified to be significantly high expressed in 42 responders than in those 28 non- responders. A prediction model was constructed by the combination of these 10 peaks, which could achieve an accuracy of 90.0% (63/70)for the chemotherapy efficiency of CRC patients. Conclusions The prediction model combined of 10 protein peaks could be helpful for prediction of the first-line chemotherapy efficiency of metastatic CRC patients.
出处 《中华结直肠疾病电子杂志》 2013年第2期19-22,共4页 Chinese Journal of Colorectal Diseases(Electronic Edition)
关键词 生物学标记 结直肠肿瘤 蛋白质阵列分析 Biological markers Colorectal neoplasms Protein array analysis
  • 相关文献

参考文献1

二级参考文献38

  • 1Koike A, Takagi T. Prediction of protein-protein interaction sites using support vector machines. Protein Eng Des Sel 2004;17:165-173.
  • 2Church TR, Yeazel MW, Jones RM, Kochevar LK, Watt GD,Mongin SJ, Cordes JE, Engelhard D. A randomized trial of direct mailing of fecal occult blood tests to increase colorectal cancer screening. J Natl Cancer Inst 2004; 96:770-780.
  • 3Kornek GV, Depisch D, Rosen HR, Temsch EM, Scheithauer W.Comparative analysis of CA72-4, CA195 and carcinoembryonic antigen in patients with gastrointestinal malignancies. J Cancer Res Clin Oncol 1992; 118:318-320.
  • 4Posner MR, Mayer RJ. The use of serologic tumor markers in gastrointestinal malignancies. Hematol Oncol Clin North Am 1994; 8:533-553.
  • 5Ohuchi N, Takahashi K, Matoba N, Sato T, Taira Y, Sakai N,Masuda M, Mori S. Comparison of serum assays for TAG-72,CA19-9 and CEA in gastrointestinal carcinoma patients. Jpn J Clin Oncol 1989; 19:242-250.
  • 6Ueda T, Shimada E, Urakawa T. The clinicopathologic features of serum CA 19-9-positive colorectal cancers. Surg Today 1994; 24:518-525.
  • 7Nakagoe T, Sawai T, Tsuji T, Jibiki MA, Nanashima A,Yamaguchi H, Yasutake T, Ayabe H, Arisawa K. Preoperative serum level of CA19-9 predicts recurrence after curative surgery in node-negative colorectal cancer patients. Hepatogastroenterology 2003; 50:696-699.
  • 8Srinivas PR, Srivastava S, Hanash S, Wright GL Jr. Proteomics in early detection of cancer. Clin Chem 2001; 47:1901-1912.
  • 9Hurlstone DP, Fujii T, Lobo AJ. Early detection of colorectal cancer using high-magnification chromoscopic colonoscopy.Br J Surg 2002; 89:272-282.
  • 10Vogelstein B, Fearon ER, Hamilton SR, Kern SE, Preisinger AC, Leppert M, Nakamura Y, White R, Smits AM, Bos JL. Genetic alterations during colorectal-tumor development. N Engl J Med 1988; 319: 525-532.

共引文献29

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部