期刊文献+

多肿瘤标志物蛋白芯片检测系统在消化道恶性肿瘤的临床应用价值 被引量:12

Clinical Application Value of Multi-tumor Markers Protein Chip Detective System in The Diagnosis of Digestive Tract Malignancies
下载PDF
导出
摘要 目的研究多肿瘤标志物蛋白芯片检测系统在消化道恶性肿瘤的普查、诊断及预后判断的临床价值。方法采用C-12蛋白芯片技术检测96例常见消化道恶性肿瘤患者组,87例消化道良性疾病患者组,120例健康查体者组血清中12项肿瘤标志物表达水平及阳性率,及51例消化道恶性肿瘤患者术后12项肿瘤标志物表达水平。结果消化道恶性肿瘤组肿瘤标志物C-12检测结果及阳性率明显高于良性疾病组及健康查体组,差异有显著性(P<0.05);12项联合检测阳性率(61.1%-82.3%)明显高于单项检测阳性率(27.72%-70.5%);消化道恶性肿瘤患者术前及部分患者术后C-12检测结果比较,差异也有显著性(P<0.05);C-12中CA199、CEA、CA242、FER、AFP、CA125、CA153等7项在恶性消化道肿瘤中表达明显高于其余几项肿瘤标志物(P<0.05)。结论多肿瘤标志物蛋白芯片检测系统用于恶性消化道肿瘤的普查、早期诊断及术后疗效观察,有一定的临床价值。 Objective To investigate the clinical application value of multi-tumor markers protein chip detective system in the diagnosis of digestive tract malignancies or prognosis judgment.Methods The expression of twelve tumor markers in serum were detected by protien chip technology in 96 cases of malignant tumor of digestive tract cancer,87cases of benign digestive diseases,120 cases of healthy persons and 51 casts of postoperative malignant tumor of digestive tract cancer.Results The expression and the positive of twelve tumor markers in the malignant tumor group was significantly higher than that of the benign diseases group and healthy group,the differences were statistically significant(P0.05);The positive ratio(61.1%-82.3%) of twelve combined detection was significantly higher than of single tumor maker(27.72%-70.5%);There were significant differences of malignant tumor of digestive trace cancer between preoperative patients and postoperative patients(P0.05);The expression of twelve tumor markers CA199、CEA、CA242、FER、AFP、CA125 and CA153 in digestive tract cancer was markedly stronger than others(P0.05).Conclusion There was clinical application value of multi-tumor marker protein chip detective system on general survey、early diagnosis and prognosis judgment in malignant tumor of digestive trace cancer.
出处 《中国实验诊断学》 北大核心 2011年第7期1111-1113,共3页 Chinese Journal of Laboratory Diagnosis
关键词 多肿瘤标志物 蛋白芯片 消化道恶性肿瘤 multi-tumor marker protein chip digestive tract malignancies
  • 相关文献

参考文献7

  • 1PatkinDM,BrayF,Pisari P Global caner statitics 2002[J].CACancer J C1in2005,55(2):74.
  • 2范公忍,任永强,邓涛,陈天宝,胡大荣.蛋白芯片检测肿瘤标志物的临床应用[J].肿瘤防治研究,2007,34(2):152-153. 被引量:4
  • 3Weintmrger SR,Dalmaaso EA, FartSET. Curtent aehievemam using Protein Oiip Array teehnolosy[ J]. Curt Opin Chem Biol,2002,6( 1 ) : 86.
  • 4Daeie S Molecular protiling of lung earcinotrm, identifying clinically useful tumomuukers for dlagnosis and prognosis [J] ,Expert RevMol Diagn,2007, 7(1) ,77.
  • 5张曙于,张金华.联合检测多项肿瘤标志物对原发性肝癌诊断价值的探讨[J].临床医学,2003,23(10):15-16. 被引量:11
  • 6Von Eggeling F, Daviel H, Lomas Let al,Tiseue-spaxdfic microdisescetin with eotlpled with protein Chip array tevhnolosiem: applicatiom in cancer research[J]. Biotedmiques,2000,29(5): 1066.
  • 7Fleisher M.Dristisn AM Sturgeon CM,et al,Prscice guidellne, Hnd reeommendatlons for use tumor markm in the elinie [J]. Washington De: AAGC preM,2002,20,.

二级参考文献11

  • 1吴健民.对肿瘤标志物的再认识[J].中华检验医学杂志,2005,28(1):11-13. 被引量:116
  • 2于皆平 沈志祥 罗和生 主编.实用消化病学 第1版[M].北京:科学出版社,1990.1073~1074.
  • 3王金标 谭夭秩 粱正路 等.血清铁蛋白放射免疫测定肝病的诊断意义[J].中华内科杂志,1986,25:649-651.
  • 4Chedid D. Antigenic marks of hepatic Cellular Carcinoma, Cancer, 1990,65:84-87.
  • 5Chapman K.The Protein Chip Biomarker System from Cipheren Bio systems:a novel proteomics platform for rapid biomarker discovery and validation[J].Biochem Soc Trans,2002,30(2):82-85.
  • 6Rubin RB,Merchant M.A rapid protein profiling system that speeds study of cancer and other diseases[J].Am Clin Lab,2000,19(8):28-32.
  • 7Fleisher M,Dnistrian AM,Sturgeon CM,et al.Practice guidelines and recommendations for use tumor markers in the clinic[J].Washington Dc:AACC press,2002,20-25.
  • 8邹雄.肿瘤标志在肿瘤早期诊断中的研究与应用进展[J].中华检验医学杂志,2002,25(2):71-72. 被引量:97
  • 9崔建国,蔡建明,黄越承.蛋白质芯片及其应用[J].国外医学(分子生物学分册),2003,25(1):19-21. 被引量:15
  • 10齐军,车轶群.使用多肿瘤标志物蛋白质芯片诊断系统检测卵巢肿瘤[J].中华检验医学杂志,2003,26(6):358-360. 被引量:47

共引文献13

同被引文献100

引证文献12

二级引证文献47

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