大肠癌明胶酶和TGF-β1及其受体的表达  被引量:1

Expression of Gelatinases and their Relationship with TGF-β1 and TGF-β1RⅠ in Colon Cancer

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作  者:侯德法[1] 邹强[2] 郝大海[1] 

机构地区:[1]安徽省阜阳市肿瘤医院病理科,236018 [2]安徽省合肥市第二人民医院病理科,230032

出  处:《中华全科医学》2010年第5期567-568,共2页Chinese Journal of General Practice

摘  要:目的研究明胶酶(MMP-2,9)与转化生长因子(TGF-β1)及其Ⅰ型受体(TGF-β1RⅠ)在大肠癌组织中的蛋白表达及其相互关系。方法应用免疫组织化学S-P法检测89例大肠癌组织中MMP-2、MMP-9与TGF-β1、TGF-β1RⅠ蛋白的表达。结果大肠癌MMP-2、MMP-9、TGF-β1和TGF-β1RⅠ阳性率分别为67.4%、65.2%、85.4%和71.9%;MMP-2表达与肿瘤大小和淋巴结转移均呈正相关(均P<0.01),MMP-9表达与淋巴结转移呈正相关(P<0.01),TGF-β1RⅠ的表达与淋巴结转移呈负相关(P<0.01);TGF-β1表达状况与MMP-2和MMP-9的表达均呈显著正相关(r=0.256和0.365,P<0.05和0.001),TGF-β1RⅠ和MMP-9的表达呈显著正相关(r=0.225,P<0.05)。结论MMP-2,9的表达情况与大肠癌侵袭转移有密切关系。MMP-2,9的表达与TGF-β1、TGF-β1RⅠ关系密切,可能在一定程度上受到TGF-β1及其受体的调控。Objective To investigate the protein expression of MMP-2,MMP-9,TGF-β1 and TGF-β1RⅠ and its clincopathological features and the relationship between them in colon cancer.Methods The protein expression of MMP-2,MMP-9,TGF-β1 and TGF-β1RⅠ were examined on tissue chips which containing 89 cases of colon carcinoma by S-P immunohistochemical method.Results The positive rates of MMP-2,MMP-9,TGF-β1 and TGF-β1RⅠ protein were 67.4%,65.2%,85.4% and 71.9%,respectively.The expression of MMP-2 was positively correlated to lymph node metastasis and tumor size(both P〈0.01).The expression levels of MMP-9 was positively correlated to lymph node metastasis(P〈0.01).The expression levels of TGF-β1RⅠ was negatively correlated to lymph node metastasis(P〈0.01).Both the expression of MMP-2 and MMP-9 was positively correlated to that of TGF-β1(r=0.256 and 0.365,P〈0.05 and P〈0.01,respectively),and MMP-9 was also positively correlated to the expression of TGF-β1RⅠ(r=0.225,P〈0.05).Conclusion The expression of MMP-2 and MMP-9 might be close correlated to the invasion and metastasis in colon cancer.The expression of MMP-2 and MMP-9 had a close relationship with TGF-β1 and TGF-β1RⅠ.The levels of MMP-2 and MMP-9 might be partly regulated by TGF-β1 and TGF-β1RⅠ.

关 键 词:大肠肿瘤 基质金属蛋白酶 转化生长因子Β1 转化生长因子β1Ⅰ型受体 免疫组织化学 

分 类 号:R735.34[医药卫生—肿瘤] R349.7[医药卫生—临床医学]

 

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