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基质金属蛋白酶及其抑制剂在非小细胞肺癌组织中的表达及临床意义 被引量:7

Clinical significance and expressions of matrix metalloproteinases and their inhibitors in NSCLC
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摘要 目的:探讨MMP-2、MMP-9、TI MP-1和TI MP-2在非小细胞肺癌(non-small cell lung cancer,NSCLC)组织中的表达及临床意义。方法:用免疫组化法测定124例NSCLC组织、124例癌旁组织和10例良性肺病组织(错构瘤)中MMP-2、MMP-9、TI MP-1和TI MP-2的表达。结果:在NSCLC组织中,MMP-2、MMP-9、TI MP-1和TI MP-2表达水平显著高于癌旁组织和良性肿瘤(P均<0.05)。MMP-2在鳞癌组织中的表达水平显著高于腺癌和腺鳞癌(P<0.05);TI MP-2在鳞癌中的表达水平显著高于腺癌(P<0.05);MMP-9和TI MP-1在腺癌组织中的表达水平显著高于鳞癌(P<0.05)。在NSCLC组织中,随着TNM分期增加,MMP-2、MMP-9、TI MP-1和TI MP-2的表达水平增加(P均<0.05)。MMP-2、MMP-9、TI MP-1和TI MP-2在淋巴结转移组中的表达水平显著高于无淋巴结转移组(P均<0.05)。MMP-2、MMP-9、TI MP-1和TI MP-2在低分化组中的表达水平显著高于高分化组(P均<0.05)。MMP-9在女性组中的表达水平显著高于男性组(P<0.05)。MMP-2、MMP-9、TI MP-1和TI MP-2之间的表达水平呈显著性正相关(P均<0.05)。结论:MMP-2、MMP-9、TI MP-1和TI MP-2均参与NSCLC的形成且与NSCLC临床病理特征关系密切,同时可能是判断预后的较好评价指标。 OBJECTIVE: To investigate the expressions of MMP-2, MMP-9, TIMP-1 and TIMP-2 and their clinical value in non-small cell lung cancer (NSCLC). METHODS: The expressions of MMP-2, MMP-9, TIMP-1 and TIMP-2 were detected in 124 NSCLC, 124 adjacent non-cancerous lung tissues and 10 benign pulmonary tissues by the immunohistochemical method. RESULTS: The expressions of MMP-2, MMP-9, TIMP-1 and TIMP-2 in NSCLC were significantly higher than those in adjacent non-cancerous lung tissues and benign pulmonary tissues (P〈0.05). the expression of MMP-2 in squamous carcinoma was significantly higher than that in adenocarcinoma and adenosquamous carcinoma (P〈0.05); the expressions of TIMP-2 in squamous carcinoma was significantly higher than that in adenocarcinoma (P〈0.05); the expression of MMP-9 and TIMP-1 in adenocarcinoma were significantly higher than those in squamous carcinoma (P〈0.05). In NSCLC, there were significant increases of MMP-2, MMP-9, TIMP-1 and TIMP-2 along with the elevation of TNM grade (P〈 0.05). Compared with the eases without lymph node and/or distant metastasis, the expressions of MMP-2, MMP-9, TIMP-1 and TIMP-2 were significantly higher in the eases with lymph node and/or distant metastasis (P〈0. 05). The expressions of MMP-2, MMP-9, TIMP-1 and TIMP-2 were related to the histological differentiation (P〈0. 05). The expression of MMP-9 in women was higher than that in men (P〈0. 05). The expressions of MMP-2, MMP-9, TIMP-1 and TIMP-2 had a significantly positive correlation with each other (P〈0.05). CONCLUSIONS: MMP-2, MMP-9, TIMP-1 and TIMP-2 are participated in the carcinogenesis of NSCLC. They have close relations with the pathological characteristics of NSCLC and might have important prognosis for NSCLC.
出处 《中华肿瘤防治杂志》 CAS 2007年第10期758-761,共4页 Chinese Journal of Cancer Prevention and Treatment
关键词 非小细胞肺 基质金属蛋白酶类 金属蛋白酶类组织抑制剂 免疫组织化学 non-small cell lung, carcinoma matrix metalloproteinases tissue inhibitor of metallaproteinases immunohistochemistry
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  • 1Curran S,Murray GI,Matrix metalloproteinases in tumour invasion and metastasis,J Pathol 1999;189:300-308.
  • 2Chakraborti S,Mandal M,Das S,Mandal A,Chakraborti T.Regulation of matrix metalloproteinases:An overview.Mol Cell Biochem 2003:253: 269-285.
  • 3Yoon SO,Park SJ,Yun CH,Chung AS.Roles of matrix metalloproteinases in tumor metastasis and angiogenesis.J Biochem Mol Biol 2003; 36:128-137.
  • 4Zucker S,Vacirca J.Role of matrix metalloproteinases(MMPs) in colorectal cancer.Cancer Metastasis Rev 2004;23:101-117.
  • 5Lynch CC,Matrisian LM,Matrix metalloproteinases in tumor-host cell communication,Differentiation 2002;70:561-573.
  • 6Vlsse R,Nagase H.Matrix metalloproteinases and tissue inhibitors of metalloproteinases:structure,function and biochemistry.Circ Res 2003;92:82;-839.
  • 7Egeblad M,Werb Z.New functions for the matrix metalloproteinases in cancer progression.Nature 2002;3:161-174.
  • 8Johansson N,Ahonen M,Kahari VM,Matrix metalloproteinases in tumor invasion,CLMS 2000;57:5-15.

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