Shi Y, Parhar R S, Zou M, Hammami M M, Akhtar M, Lum Z P, Farid N R, Al-Sedairy S T, Paterson M C
Department of Biological and Medical Research, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Br J Cancer. 1999 Mar;79(7-8):1234-9. doi: 10.1038/sj.bjc.6690198.
Tumour cell invasion and metastasis is a multistep process that involves the degradation of extracellular matrix proteins by matrix metalloproteinases (MMPs). Tissue inhibitors of metalloproteinases (TIMPs) act as negative regulators of MMPs and thus prevent tumour cell invasion and metastasis by preserving extracellular matrix (ECM) integrity. In the present study we examined the expression of one member of TIMPs, TIMP-1, in 39 thyroid tumour specimens and two thyroid carcinoma cell lines (NPA and SW579). We also investigated the effect of high TIMP-1 expression on the invasive potential of NPA cells. Northern blot analysis showed that TIMP-1 mRNA levels correlated directly with tumour aggressiveness: the highest number of TIMP-1 transcripts was found in stages III and IV vs benign goitre (P < 0.0001). However, TIMP-1 expression was not increased in NPA and SW579 cells, both of which are derived from poorly differentiated thyroid tumours. Immunohistochemical study showed strong TIMP-1 staining in the stroma cells of advanced stages of carcinomas. Overexpression of TIMP-1 by gene transfer resulted in a significant suppression of the malignant phenotype of NPA cells as judged by an in vitro tumour invasion assay. These results suggest that high levels of TIMP-1 transcripts in advanced stages of thyroid carcinoma likely come from stroma rather than thyroid cancer cells, and TIMP-1 may function as a thyroid tumour invasion/metastasis suppressor.
肿瘤细胞侵袭和转移是一个多步骤过程,涉及基质金属蛋白酶(MMPs)对细胞外基质蛋白的降解。金属蛋白酶组织抑制剂(TIMPs)作为MMPs的负调节因子,通过维持细胞外基质(ECM)的完整性来阻止肿瘤细胞侵袭和转移。在本研究中,我们检测了39例甲状腺肿瘤标本和两种甲状腺癌细胞系(NPA和SW579)中TIMPs的一个成员TIMP-1的表达。我们还研究了TIMP-1高表达对NPA细胞侵袭潜能的影响。Northern印迹分析表明,TIMP-1 mRNA水平与肿瘤侵袭性直接相关:在III期和IV期肿瘤中发现的TIMP-1转录本数量最多,与良性甲状腺肿相比(P < 0.0001)。然而,NPA和SW579细胞中TIMP-1的表达并未增加,这两种细胞系均来源于低分化甲状腺肿瘤。免疫组织化学研究显示,在癌晚期的基质细胞中有强烈的TIMP-1染色。通过基因转移使TIMP-1过表达,根据体外肿瘤侵袭试验判断,导致NPA细胞的恶性表型显著受到抑制。这些结果表明,甲状腺癌晚期TIMP-1转录本的高水平可能来自基质而非甲状腺癌细胞,并且TIMP-1可能作为甲状腺肿瘤侵袭/转移抑制因子发挥作用。