Mino Nobuya, Takenaka Kazumasa, Sonobe Makoto, Miyahara Ryo, Yanagihara Kazuhiro, Otake Yosuke, Wada Hiromi, Tanaka Fumihiro
Department of Thoracic Surgery, Faculty of Medicine, Kyoto University, Kyoto, Japan.
J Surg Oncol. 2007 Mar 1;95(3):250-7. doi: 10.1002/jso.20663.
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).
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.
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).
TIMP-3 expression status was significantly correlated with pathologic stage and nodal involvement, and was an independent prognostic factor in resected NSCLC.
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。
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。
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)。
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。