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多效蛋白在恶性胸腔积液中的诊断价值 被引量:3

The Diagnostic Value for Lung Cancer by Detecting the Levels of Pleiotrophin in the Pleural Effusions
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摘要 目的研究良恶性胸腔积液多效蛋白(PTN)的表达,探讨多效蛋白对肺癌的诊断价值。方法分别采用双抗体夹心酶联免疫吸附实验法检测肺癌组50例、良性组50例患者胸腔积液中PTN、癌胚抗原(CEA)的表达水平。结果①恶性胸腔积液组PTN表达水平显著高于良性组([47.744±40.007)ng/mL vs(3.719±1.827)ng/mL,P<0.001],胸腔积液PTN含量测定对恶性胸腔积液的诊断效能略差于CEA。结论胸腔积液PTN对肺癌合并恶性胸腔积液有一定的诊断价值,PTN、CEA联合检测有助于临床诊断。 Objective To investigate the expression of Pleiotrophin in the pleural effusions of patients with benign and malignant diseases, carcinoembryonic antigen(CEA), and to study the diagnostic vaule of Pleiotrophin for lung cancer. Methods Pleiotrophin, CEA levels in pleural effusions were measured respectively in benign diseases(n=50) and lung cancer patients(n=50) by using sandwich enzymelinked immunosorbent assay(ELISA). Results The concentration of Pleiotrophin was significantly higher in malignant pleural effusions due to lung cancer(47.744 ± 40.007) than that in benign group(3.719 ± 1.827ng/ml), P〈 0.001. Pleiotrophin was slightly less valuable than CEA in the diagnosis of malignant pleural effusions. Conclusion Pleiotrophin may be an useful marker to differentiate between benign and malignant pleural effusions. The combined detection of two indicators-Pleiotrophin,CEA in the pleural effusions were of important clinical significance in the diagnosis of lung cancer.
作者 谢海燕 姜藻
出处 《中国现代医生》 2009年第6期29-31,37,共4页 China Modern Doctor
关键词 胸腔积液 多效蛋白 肺癌 癌胚抗原 Pleural effusion Pleiotrophin Lung cancer Carcinoembryonic antigen
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  • 1Liliental J,Moon SY,Lesche R,et al.Genetic deletion of the pten tumor suppressor gene promotes cell motility by activation of Pacl and Cdc42 GTPases[J].Curr Biol,2000,10(7):401-404.
  • 2Kilpelkinen I,Kaksonen M,Kinnunen T,et al.Heparin-binding growth-associated molecule contains two heparin-binding β-sheet domains that are homologous to the thrombospondin type Ⅰ repeat[J].J Biol Chem,2000,275(18):13564-13570.
  • 3Polykratis A,Delbe J,Courty J,et al.Identification of heparin affin regulatory peptide domains with potential role on angiogenesis[J].Int J Biochem Cell Biol,2004,36(10):1954-1966.
  • 4American Thoracic Society.Management of malignant pleural effusions[J].Am J Respir Crit Care Med,2000,162(5):1987-2001.
  • 5Maskell NA,Butland RJ.BTS guidelines for the investigation of a unilateral pleural effusion in adults[J].Thorax,2003,58(Suppl 2):ii8-17.
  • 6Yeh HJ,He YY,Xu J,et al.Upregulation of pleiotrophin gene expression in developing microvasculature,macrophages,and astrocytes after acute ischemic brain injury[J].J Neurobiol,1998,18(10):3699-3707.
  • 7Chondhuri R,Zhang HT,Donnini S,et al.An angioginic role for the neurokine midkine and pleiotrophin in tumorigenesis[J].Cancer Res,1997,57(9):1814-1819.
  • 8Sack U,Hoffmann M,Zhao XJ,et al.Vascular endothelial growth factor in pleural effusions of different origin[J].Eur Respir J,2005,25(4):600-604.
  • 9Milner PG,Li YS,Hoffman RM,et al.A novel 17 kD heparin-binding growth factor (HBGF-8) in bovine uterus:purification and N-terminal amino acid sequence[J].Biochem Biophys Res Commun,1989,165(3):1096-1103.
  • 10Deuel TF,Zhang N,Yeh HJ,et al.Pleiotrophin:a cytokine with diverse functions and a novel signaling pathway[J].Arch Biochem Biophys,2002,397(2):162-171.

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  • 1张宏艳,李刚,宋三泰.Pleiotrophin研究进展[J].国外医学(遗传学分册),2005,28(2):65-68. 被引量:9
  • 2Bernard I, Dellbe J,Caruelle D, et al. The lysine-rich C-terminaltail of heparin affin regulatory pcptide is required for mitogenic and tumor formation activities [ J ]. Biol Chem, 2001,276 : 228- 234.
  • 3Macey T, Lowe J, Chavkin C. Mu opioid receptor activation of ERK1/2 is GRK3 and arrestin dependent in striatal neurons[J]. J Biol Chem 2006 28(45) :34515-34524.
  • 4Seo J, Ahn Y,Lee S, et al. The major target of the endogenously generated reactive oxygen species in response to insulin stimulation is phosphatase and tensin homolog and not phosphoinositide- 3 kinase in the PI-3 kinase/Akt pathway [ J]. Mol Biol Cell, 2005,16:348-357.
  • 5Rauvala H, Huttunen H, Fages C,et al. Heparin-binding proteins HB-GAM (pleiotrophin) and amphoterin in the regulation of cell motility [ J ]. Matrix Biol,2000,19 ( 5 ) :377-387.
  • 6Bhat-Nakshatri P, Newton T,Goulet R, et al. NF-kappa B activation and interleukin 6 production in fibroblasls by estrogen receptor-negative breast cancer cell-derived interleukin lalpha [ J ]. Med Sci, 1998,95:6971-6976.
  • 7Merenmies J, Rauvala H. Molecular cloning of the 18-kDa growth- associated protein of developing brain[ J]. Biol Chem, 1990,265 (28) : 16721-16724.
  • 8Kurlz A,Schulte A, Wellstein A. Pleiotrophin and midkine in normal development and tumor biology[ J]. Crit Rev Oncog, 1995,6 (2) :151-177.
  • 9Mikelis C, Koutsioumpa M, Papadimitriou E. Pleiotmphin as a possible new target for angiogenesis-relaled diseases and cancer [ J]. Recent Patents Anticaneer Drug Discov, 2007,2 ( 2 ) : 175- 186.
  • 10Ardizzoni A, CaferataMA,TiseoM,et al. Decline in serum carcinoembryonic antigen anti cytokeratin 19 fragment during chemotherapy predictsobjective response and survival in patients with advanced nonsmall cell lung cancer[ J]. Cancer,2006,107( 12 ) : 28-42.

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