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p-p38和uPA在胃癌组织中的表达及意义 被引量:3

The Expressions of p-p38 and Urokinase-Type Plasminogen Activator and Their Significance in Gastric Carcinoma
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摘要 目的研究磷酸化p38(p-p38)和尿激酶型纤溶酶原激活剂(uPA)在胃癌组织中的表达及与临床病理特征的关系。方法采用免疫组织化学方法检测35例胃癌组织标本中p-p38和uPA的表达并分析其相关性及与临床病理特征进行比较。结果胃癌组织中p-p38及uPA的阳性表达率分别为62.9%和60.0%。p-p38和uPA表达均为阳性17例,表达均为阴性9例,两者表达一致的符合率为74.3%(26/35),其表达呈密切相关(P<0.05);两者与胃癌的浸润程度、淋巴结转移密切相关(P<0.05),而与患者年龄、性别无显著相关性(P>0.05)。结论p-p38及uPA过表达在胃癌的发展及浸润转移中具有重要的作用,p-p38和uPA的表达可辅助用于胃癌的预后评估。 Objective To study the expressions of phosphorylated p38 (p-p38)and urokinase-type plasminogen activator(uPA) and their relationship with the clinicopathological features in gastric carcinoma. Methods The expressions of p-p38 and uPA were determined by immunohisto-chemical method in 35 cases with gastric carcinoma . The relationship between the expressions of p-p38 and uPA and the clinicopathological features was analyzed. Results The positive expression rates of p-p38 and uPA in gastric carcinoma were 62.9% and 60.0%. Both p-p38 and uPA expressions were positive in 17 cases and negative in 9 cases. There was a close relationship between the p-p38 and uPA expressions. The expressions of p-p38 and uPA were correlated with development, infiltration and lymph node metastasis, but no relationship was found between their expressions and the patient' s age and sex. Conclusions The overexpressions of p-p38 and uPA play an important role in the development, invasion, and metastasis of stomach cancer.
出处 《肿瘤基础与临床》 2008年第2期116-118,共3页 journal of basic and clinical oncology
关键词 磷酸化P38 尿激酶型纤溶酶原激活剂 胃癌 phosphorylated p38 urokinase-type plasminogen activator gastric carcinoma
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  • 1Tyler ZARUBIN.Activation and signaling of the p38 MAP kinase pathway[J].Cell Research,2005,15(1):11-18. 被引量:158
  • 2Wang XZ, Ron D. Stress-induced phosphorylation and activation of the transcription factor CHOP (GADD153) by p38 MAP Kinase. Science, 1996,272:1347-1349.
  • 3Li G, Chen SJ, Oparil S, et al. Direct in vivo evidence demonstrating neointimal migration of adventitial fibroblasts after balloon injury of rat carotid arteries. Circulation,2000,101:1362-1365.
  • 4Siow RC, Mallawaarachchi CM, Weissberg PL. Migration of adventitial myofibroblasts following vascular balloon injury: insights from in vivo gene transfer to rat carotid arteries. Cardiovasc Res, 2003,59:212-221.
  • 5Zhan Y, Kim S, Izumi Y,et al. Role of JNK, p38, and ERK in platelet-derived growth factor-induced vascular proliferation, migration, and gene expression. Arterioscler Thromb Vasc Biol,2003,23: 795-801.
  • 6Olsson N, Piek E, Sundstrom M,et al. Transfor ming growth factor-beta-mediated mast cell migration depends on mitogen-activated protein kinase activity. Cell Signal,2001,13:483-490.
  • 7Li S, Moon JJ, Miao H,et al. Signal transduction in matrix contraction and the migration of vascular smooth muscle cells in three-dimensional matrix. J Vasc Res,2003,40:378-388.
  • 8Chaulet H, Desgranges C, Renault MA,et al. Extracellular nucleotides induce arterial smooth muscle cell migration via osteopontin. Circ Res,2001,89:772-778.
  • 9Moon MC, Molnar K, Yau L. Perivascular delivery of losartan with surgical fibrin glue prevents neointimal hyperplasia after arterial injury. J Vasc Surg,2004, 40:130-137.
  • 10Ng DC, Court NW, dos Remedios CG,et al. Activation of signal transducer and activator of transcription (STAT) pathways in failing human hearts. Cardiovasc Res, 2003,57:333-346.

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