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III期非小细胞肺癌中C-12的检测及其预后意义 被引量:3

Detection of multiple tumor marker protein biochip and its prognostic significance in non-small cell lung cancer patients in stage III.
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摘要 目的探讨多种肿瘤标志物蛋白芯片检测系统(C-12)在III期非小细胞肺癌的病情监测、治疗反应观察和预后评估中的意义。方法应用该芯片检测系统测定57例III期非小细胞肺癌病人化疗前后血清中12种肿瘤标志物(CA19-9,NSE,CEA,CA242,Fe,HCG,AFP,FPSA,PSA,CA125,HGH,CA15-3)的水平,观察化疗疗效与C-12的关系。结果57例病人中不同疗效组患者自身前后对照,其血清肿瘤标志物水平和C-12总阳性率无显著性差异;在剔除各组中C-12阴性病例后,PR组中的C-12阳性病人治疗后有CA19-9、CA15-3及Fe显著性降低(P<0.05),而NC组中的C-12阳性病人各项肿瘤标志物水平在化疗后均无明显变化。结论该检测系统在监测C-12阳性肺癌的治疗效果方面有一定的指导意义,如作适当改进,将能更有效地运用于临床。 Objective To investigate the significance of multiple tumor marker protein biechip detective system in monitoring therapeutic efficacy and evaluating prognosis in non - small cell lung cancer patients in stage Ⅲ. Methods From March 2003 to December 2004, 57 cases of non - small cell lung cancer patients in stage Ⅲ were investigated. All cases underwent chemotherapy, before and after treatment, the serum levels of 12 tumor markers( C - 12) including CA19-9,NSE,CEA,CA242, Fe,HCG,AFP, FPSA,PSA,CA125,HGH and CA15-3, were measured , its relation to therapeutic efficacy was observed. Results Of the 57 treated patients, 27 patients had partial response (PR) and 21 patients had no change( NC) ,9 patients had progressive disease(PD) ,but no patient had complete response( CR). There were no remarkable differences in serum levels of C - 12 after chemotherapy. After excluding the patients who were negative to C - 12, the serum levels of CA19 -9,CA15 -3 and Fe in PR group were significanter lower after chemotherapy ( P 〈 0.05 ) , but no remarkable difference in NC group. Conclusion The multiple tumor marker protein biochip detective system may play a role in monitoring therapeutic efficacy in C - 12 positive lung cancer , it maybe a useful monitor marker to C - 12 positive lung cancer patients.
机构地区 湖南省肿瘤医院
出处 《现代肿瘤医学》 CAS 2006年第3期281-283,共3页 Journal of Modern Oncology
关键词 非小细胞肺癌 肿瘤标志物 多种肿瘤标志物蛋白芯片 蛋白芯片 non -small cell lung cancer tumor marker multiple tumor marker protein biochip protein biochip
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参考文献10

  • 1左强,张军一,郑航,李黎波,饶芬玲,罗荣城,李金瀚.多种肿瘤标志物蛋白芯片检测系统对肺癌的诊断价值[J].中国肺癌杂志,2004,7(2):154-157. 被引量:26
  • 2Weinberger SR,Dalmasso EA,Fung ET.Current achievements using ProteinChip Array technology[J].Curr Opin Chem Biol,2002,6:86~91.
  • 3Ando S,Suzuki M,Yamamoto N,et al.The prognostic value of both neuron-specific enolase (NSE) and Cyfra21-1 in small cell lung cancer[J].Anticancer Res,2004,24:1941~1946.
  • 4Ando S,Kimura H,Iwai N,et al.Optimal combination of seven tumour markers in prediction of advanced stage at first examination of patients with non-small cell lung cancer[J].Anticancer Res,2001,21:3085~3092.
  • 5Sawabata N,Maeda H,Yokota S,et al.Postoperative serum carcinoembryonic antigen levels in patients with pathologic stage IA nonsmall cell lung carcinoma:subnormal levels as an indicator of favorable prognosis[J].Cancer,2004,101:803~809.
  • 6Milman N,Pedersen LM.The serum ferritin concentration is a significant prognostic indicator of survival in primary lung cancer[J].Oncol Rep,2002,9:193~198.
  • 7Muley T,Dienemann H,Ebert W.CYFRA 21-1 and CEA are independent prognostic factors in 153 operated stage I NSCLC patients[J].Anticancer Res,2004,24:1953~1956.
  • 8Schneider J,Peltri G,Bitterlich N,et al.Fuzzy logic-based tumor marker profiles including a new marker tumor M2-PK improved sensitivity to the detection of progression in lung cancer patients[J].Anticancer Res,2003,23:899~906.
  • 9Ren H,Tang X,Lee JJ,et al.Expression of hepatoma-derived growth factor is a strong prognostic predictor for patients with early-stage non-small-cell lung cancer[J].J Clin Oncol,2004,22:3230~3237.
  • 10Yamayoshi T,Nagayasu T,Matsumoto K,et al.Expression of keratinocyte growth factor/fibroblast growth factor-7 and its receptor in human lung cancer:correlation with tumour proliferative activity and patient prognosis[J].J Pathol,2004,204:110~118.

二级参考文献10

  • 1[1]von Eggeling F, Davies H, Lomas L, et al. Tissue-specific microdissection coupled with ProteinChip array technologies: applications in cancer research. Biotechniques,2000,29(5):1066-1070.
  • 2[2]Weinberger SR, Dalmasso EA, Fung ET. Current achievements using ProteinChip Array technology. Curr Opin Chem Biol,2002,6(1):86-91.
  • 3[3]Rubin RB, Merchant M. A rapid protein profiling system that speeds study of cancer and other diseases. Am Clin Lab,2000,19(8):28-29.
  • 4[4]Schneider J, Peltri G, Bitterlich N, et al. Fuzzy logic-based tumor marker profiles including a new marker tumor M2-PK improved sensitivity to the detection of progression in lung cancer patients.Anticancer Res,2003,23(2A):899-906.
  • 5[5]Sosnowski RG, Tu E, Butler WF, et al. Rapid determination of single base mismatch mutations in DNA hybrids by direct electric field control. Proc Natl Acad Sci USA,1997,94(4):1119-1123.
  • 6[6]Livache T, Bazin H, Caillat P, et al. Electroconducting polymers for the construction of DNA or peptide arrays on silicon chips. Biosens Bioelectron,1998,13(6):629-634.
  • 7[7]Chapman K. The ProteinChip Biomarker System from Ciphergen Biosystems: a novel proteomics platform for rapid biomarker discovery and validation. Biochem Soc Trans,2002,30(2):82-87.
  • 8[8]Lin S, Tornatore P, King D, et al. Limited acid hydrolysis as a means of fragmenting proteins isolated upon ProteinChip array surfaces.Proteomics,2001,1(9):1172-1184.
  • 9[9]von Eggeling F, Junker K, Fiedle W, et al. Mass spectrometry meets chip technology: a new proteomic tool in cancer research? Electrophoresis,2001,22(14):2898-2902.
  • 10[10]Kulpa J, Wojcik E, Reinfuss M, et al. Carcinoembryonic antigen, squamous cell carcinoma antigen, CYFRA 21-1, and neuron-specific enolase in squamous cell lung cancer patients. Clin Chem,2002,48(11):1931-1937.

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