检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:刘君[1] 黄凤德[1] 胡晋太[1] 岳明全[1]
出 处:《现代中西医结合杂志》2015年第27期2968-2970,共3页Modern Journal of Integrated Traditional Chinese and Western Medicine
摘 要:目的探讨乳腺浸润性导管癌(IDC)组织磷酸化蛋白激酶B(p-AKT)、血管内皮细胞生长因子-C(VEGF-C)表达水平,及其与淋巴结侵袭转移的关系。方法应用免疫组织化学法检测72例乳腺IDC组织及30例乳腺腺瘤组织中p-AKT、VEGF-C的表达水平,分析p-AKT与血管生成的关系。结果乳腺IDC组织中VEGF、p-AKT蛋白的阳性表达率分别为59%和67%,均显著高于乳腺腺瘤组织中20%和17%的阳性表达率(X2=13.39,21.21,P<0.05);与有淋巴结转移者比较,无淋巴结转移的乳腺IDC组织VEGF-C、pAKT蛋白阳性表达率显著降低(X2=11.10,5.51,P<0.05);乳腺IDC组织VEGF-C、pAKT蛋白表达水平呈显著正相关(r=0.823,P<0.05)。结论乳腺IDC组织中VEGF-C、pAKT呈过度表达状态,共同参与淋巴结的侵袭与转移,阻断PI3K/AKT通路有望为乳腺IDC的靶向治疗提供一种新的思路。Objective It is to investigate the expression of vascular endothelial growth factor ( VEGF), protein kinase B (P- AKT) in breast invasive ductal carcinoma (IDC) , and its relation with lymph node invasion and metastasis. Methods The expression of p - AKT, VEGF - C in the tissue of 72 cases of breast IDC and 30 cases of breast fibroadenoma were detec- ted by immunohistochemical staining, the correlation between p -AKT and angiogenesis were analyzed. Results The positive expression rate of p -AKT, VEGF- C protein in breast IDC was 59% and 67% respectively, which was significantly higher than that in breast fibroadenoma of 20% and 17% respectively ( χ 2= 13.39, 21.21, all P 〈 0. 05). The expressions of p - AKT, VEGF - C in breast IDC with lymphnode metastasis were higher than those without lymphnode metastasis (χ2= 11.10, 5.51, all P 〈 0. 05). The positive expression rate of VEGF- C had significant positive correlation with that of p -AKT (r = 0. 823, P 〈0.05 ). Conelttsion The expression of p- AKT, VEGF- C in breast IDC is over-expressive, and participate the lymphnode invasion and metastasis. Inhibition of PI3K/AKT signal transduction pathway can be expected to provide a new method for the target therapy of breast IDC.
关 键 词:乳腺浸润性导管癌 血管内皮细胞生长因子-C 磷酸化蛋白激酶B 淋巴结转移
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.128.78.139