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金属蛋白酶组织抑制剂-3(TIMP-3)在非小细胞肺癌切除标本中的表达及其预后意义

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

作者信息

Mino Nobuya, Takenaka Kazumasa, Sonobe Makoto, Miyahara Ryo, Yanagihara Kazuhiro, Otake Yosuke, Wada Hiromi, Tanaka Fumihiro

机构信息

Department of Thoracic Surgery, Faculty of Medicine, Kyoto University, Kyoto, Japan.

出版信息

J Surg Oncol. 2007 Mar 1;95(3):250-7. doi: 10.1002/jso.20663.

Abstract

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.

摘要

背景与目的

金属蛋白酶组织抑制剂-3(TIMP-3)可抑制金属蛋白酶的活性,而金属蛋白酶在恶性肿瘤的发生发展过程中发挥着重要作用。我们对手术切除的非小细胞肺癌(NSCLC)中TIMP-3的表达进行了一项回顾性研究。

方法

采用免疫组织化学方法检测了143例行NSCLC根治性切除术患者的原发性肿瘤标本中TIMP-3的表达。分析了TIMP-3表达分级与肿瘤组织学类型、TNM分期、MMP-2和MMP-9表达分级、VEGF表达分级、肿瘤内微血管密度、增殖指数、凋亡指数及预后之间的相关性。

结果

40例患者TIMP-3表达低,71例中等,32例高。鳞状细胞癌中TIMP-3表达高于腺癌(P = 0.001),TIMP-3表达降低与淋巴结受累(P = 0.016)及病理分期较晚(P = 0.036)显著相关。MMP-2表达随TIMP-3表达增强而降低(P = 0.010)。TIMP-3表达低、中、高的患者5年总生存率分别为53%、64%和84%(P = 0.037)。多因素分析证实,TIMP-3表达增强是预后良好的独立因素(P = 0.037)。

结论

TIMP-3表达状态与病理分期和淋巴结受累显著相关,是手术切除的NSCLC的独立预后因素。

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