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结直肠癌患者血清MIC-1的表达及意义 被引量:1

Expression of significance macrophage inhibitory cytokine 1 in colorectal carcinoma
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摘要 目的评价结直肠癌患者血清中巨噬细胞抑制因子1(M IC-1)的表达水平及其临床意义。方法测定152例未经放化疗结直肠癌患者及120例健康对照组的血清M IC-1、癌胚抗原(CEA)及糖链抗原19-9(CA 19-9)水平。结果结直肠癌患者血清M IC-1水平较健康对照组显著升高(P<0.01),M IC-1水平与Dukes分期、分化程度、浸润深度、淋巴转移、远处转移相关(P<0.01),与年龄、组织类型无关。M IC-1表达与CEA呈正相关(r=0.514;P<0.01),联合CEA及CA 19-9检测可提高结直肠癌诊断的敏感性和准确率。结论血清M IC-1联合CEA及CA 19-9对结直肠癌诊断和鉴别诊断有一定的临床应用价值。 [objective] To evaluate the expression of macrophage inhibitory cytokine 1 (MIC-1) in colorectal carcinoma and its clinical significance. [Methods] MIC-1,CEA and CA19-9 serum levels were determined in 152 patients with colorectal carcinoma without radiotherapy or chemotherapy and 120 normal subjects. [Results] There was a significant increase in serum MIC-1 levels in colorectal carcinoma group compared with normal controls (P〈0. 01). Serum MIC-1 level was correlated with Dukes stage, the level was higher in patients with higher Dukes stage, serum MIC-1 level had correlation with differentiation, infiltration extent, lymph node metastasis, distant metastasis (P〈0. 01), and no correlation with MIC-1 levels and age, tissue category. Serum MIC-1 was positive correlated with CEA (P〈0. 01; r= 0. 514), and combinations of CEA and CA19-9 can increase sensitivity and accuracy of colorectal carcinoma detection. [Conclusion] Serum MIC-1 measurement combined with CEA and CA19-9 can aid in diagnosis and differential diagnosis of colorectal carcinoma.
作者 郑佳 黄智铭
出处 《山东医药》 CAS 北大核心 2006年第31期7-8,共2页 Shandong Medical Journal
关键词 结肠肿瘤 直肠肿瘤 巨噬细胞抑制因子1 癌胚抗原 糖链抗原19—9 colonic neoplasms rectal neoplasms macrophage inhibitory cytokine 1 carcino-embryonic antigen carbohydrate antigen19-9
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  • 1Buckhaults P,Rago C,St Croix B,et al.Secreted and cell surface genes expressed in benign and malignant colorectal tumors[J].Cancer Res,2001,61(19):6996-7001.
  • 2Welsh JB,Sapinoso LM,Kern SG,et al.Large-scale delineation of secreted protein biomarkers overexpressed in cancer tissue and serum[J].Proc Natl Acad Sci U S A,2003,100(6):3410-3415.
  • 3Brown DA,Ward RL,Buckhaults P,et al.MIC-1 Serum Level and Genotype:Associations with Progress and Prognosis of Colorectal Carcinoma[J].Clinical Cancer Research,2003,9(7):2642-2650.

同被引文献22

  • 1王志宇,杨渤彦,窦征岳,韩强,贾琳,毕雪冰,程魏.MIC-1、VEGF和P53蛋白表达与直肠癌临床病理及预后的关系[J].中国癌症杂志,2007,17(8):607-609. 被引量:6
  • 2Bauskin AR, Bootcov MR, Valenzuela SM, et al. MIC-1 a novel macrephage inhibitory cytokine 1, is a divergent member of the TGF beta superfamily [ J ]. Proc Natl Acad Sci U S A, 1997,94 (21) :11514-11519.
  • 3Fairlie WD, Moore AG, Bauskin AR,et al. MIC-1 is a novel TGF-β Superfamily Cytokine associated with macrophage activation [ J ]. Leukocyte Biol, 1999,65 ( 1 ) :2-5.
  • 4Welsh JB, Sapinoso LM, Kern SG, et al. Large scale delineation of secreted protein biomarkers overexpressed in cancer tissue and serum[ J]. Proe Natl Acad Sci U S A,2003,100(6) :3410-3415.
  • 5Brown DA,Ward RL, Buckhaults P, et al. MIC-1 serum level and genotype: associations with progress and prognosis of colorectal carcinoma [ J ]. Clin Cancer Res, 2003,9 ( 7 ) : 2642-2650.
  • 6Graichen R,Liu D, Sun Y, et al. Autocrine human growth hormone inhibits placental transforming growth factor betagene transcription to prevent apoptosis and allow cell cycle progression of human mam- mary carcinoma ceils [ J ]. Biol Chem,2002,277 (29) :26662-26672.
  • 7Huh SJ, Chung CY, Sharma A, et al. Macrophage inhibitory cyto- kine-1 regulates melanoma vascular development[ J]. Am J Pathol, 2010,176(6) :2948-2957.
  • 8Kim KK, Lee JJ, Yang Y, et al. Macrophage inhibitory cytokine-I activities AKT and ERK1/2 via the transactivation of ErBb2 in human brest and gastric cancer cells[ J]. Carcinogenesis,2008,29 (4) :704-712.
  • 9Liu T, Bauskin AR, Zaunders J. Macrophage inhibitory cytokine-1 reduces cell adhesion and induces apoptosis in prostate cancer cells [ J]. Cancer Res ,2003,63 ( 16 ) :5034-5040.
  • 10Jang TJ, Kang H J, Kim JR,et al. Nonsteroidal antiinflammatoy drug activated gene (NAG-I) expression is closely related to death receptor-4and5 induction, which may explain sulindac sulfide induced gastric cancer cell apoptosis [ J ]. Carcinogenesis,2004,25 (10) :1853-1858.

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