...
首页> 外文期刊>Journal of Surgical Oncology >Expression of tissue inhibitor of metalloproteinase-3 (TIMP-3) and its prognostic significance in resected non-small cell lung cancer.
【24h】

Expression of tissue inhibitor of metalloproteinase-3 (TIMP-3) and its prognostic significance in resected non-small cell lung cancer.

机译:金属蛋白酶-3(TIMP-3)组织抑制剂的表达及其在切除的非小细胞肺癌中的预后意义。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND AND OBJECTIVES: Tissue inhibitor of metalloproteinase-3 (TIMP-3) inhibits the activity of metalloproteinases that play important roles in development and progression of malignant tumors. We conducted a retrospective study of TIMP-3 expression in resected non-small cell lung cancer (NSCLC). METHODS: TIMP-3 expression was examined immunohistochemically in primary tumor specimens from 143 patients who underwent complete resection for NSCLC. Correlations between TIMP-3 expression grade and tumor histology, TNM classification, MMP-2 and MMP-9 expression grade, VEGF expression grade, intra-tumoral microvessel density, proliferative index, apoptosis index, and prognosis were analyzed. RESULTS: TIMP-3 expression was low in 40, moderate in 71, and high in 32 patients. Higher TIMP-3 expression was seen in squamous cell carcinoma than in adenocarcinoma (P = 0.001), and reduced TIMP-3 expression was significantly associated with nodal involvement (P = 0.016) and advanced pathologic stage (P = 0.036). MMP-2 expression was reduced along with enhanced TIMP-3 expression (P = 0.010). The 5-year overall survival rates of low, moderate, and high TIMP-3 patients were 53, 64, and 84%, respectively (P = 0.037). Multivariate analysis confirmed that enhanced TIMP-3 expression was an independent factor for a favorable prognosis (P = 0.037). CONCLUSIONS: TIMP-3 expression status was significantly correlated with pathologic stage and nodal involvement, and was an independent prognostic factor in resected NSCLC.
机译:背景和目的:金属蛋白酶-3的组织抑制剂(TIMP-3)抑制在恶性肿瘤的发展和进展中发挥重要作用金属蛋白酶的活性。我们在切除非小细胞肺癌(NSCLC)进行TIMP-3表达的回顾性研究。从143例谁接受完全切除非小细胞肺癌免疫组织化学检查在原发性肿瘤标本TIMP-3的表达:方法。 TIMP-3表达分级和肿瘤组织学,TNM分期,MMP-2和MMP-9的表达级,VEGF表达等级,肿瘤内微血管密度,增殖指数,凋亡指数,和预后之间的相关性进行分析。结果:TIMP-3表达是低的在40,在71中度,和32例高。更高TIMP-3的表达被认为在鳞状细胞癌比腺癌(P = 0.001),和降低的TIMP-3表达与淋巴结受累(P = 0.016)和先进的病理分期(P = 0.036)中的溶液显著相关联。 MMP-2表达与增强TIMP-3的表达(P = 0.010)一起降低。低的5年生存率,中度,和高TIMP-3例分别为53,64,和84%(P = 0.037)。多元分析证实,增强TIMP-3表达是有利的预后(P = 0.037)的独立因素。结论:TIMP-3的表达状态被显著与病理阶段和淋巴结转移相关,并且是在切除的NSCLC的独立预后因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号