Dipartimento di Biologia e Patologia Cellulare e Molecolare, Federico II University of Naples, 80131 Naples, Italy.
J Clin Endocrinol Metab. 2013 Jan;98(1):228-35. doi: 10.1210/jc.2012-2528. Epub 2012 Nov 12.
We have previously identified neutrophil gelatinase-associated lipocalin (NGAL) as one of the genes mediating the oncogenic activity of nuclear factor-κB in human anaplastic thyroid carcinomas (ATCs).
To further investigate the role of NGAL in thyroid cancer, we established NGAL knocked-down and NGAL overexpressing ATC cell lines.
We found that the ability of NGAL knocked-down cells to degrade Matrigel in a transwell invasion assay and to form lung metastasis in nude mice was decreased. Because NGAL binds matrix metalloproteinase-9 (MMP-9), to form a macromolecular complex involved in the regulation of metastatic spread of cancer cells and given the strong expression of both genes in tissue specimens from human ATCs, we analyzed the MMP-9 enzymatic activity in NGAL-null ATC cells. Enzymatic immunoassays show that MMP-9 activity is reduced in NGAL-null ATC cells, even if its expression is not affected by NGAL inhibition. Ectopic expression of NGAL in an ATC cell line not expressing NGAL determines an increase of its metastatic property. The use of a mutated form of NGAL, unable to bind MMP-9, has no positive effect on the invasive potential of ATC cells and does not improve the MMP-9 enzymatic activity.
Our results indicate NGAL as a novel target of nuclear factor-κB prometastatic activity in thyroid cancer through enhancement of MMP-9 enzymatic activity.
我们之前已经确定中性粒细胞明胶酶相关脂质运载蛋白(NGAL)是核因子-κB 在人类间变性甲状腺癌(ATC)中发挥致癌活性的基因之一。
为了进一步研究 NGAL 在甲状腺癌中的作用,我们建立了 NGAL 敲低和 NGAL 过表达的 ATC 细胞系。
我们发现 NGAL 敲低细胞在 Transwell 侵袭实验中降解 Matrigel 和在裸鼠中形成肺转移的能力降低。因为 NGAL 与基质金属蛋白酶-9(MMP-9)结合,形成一个参与调节癌细胞转移扩散的大分子复合物,并且这两个基因在人 ATC 组织标本中均强烈表达,所以我们分析了 NGAL 缺失的 ATC 细胞中的 MMP-9 酶活性。酶免疫测定显示,即使 NGAL 抑制不影响其表达,NGAL 缺失的 ATC 细胞中的 MMP-9 活性也降低。在不表达 NGAL 的 ATC 细胞系中异位表达 NGAL 会增加其转移特性。使用不能结合 MMP-9 的突变形式的 NGAL 对 ATC 细胞的侵袭潜能没有积极影响,也不能提高 MMP-9 的酶活性。
我们的结果表明,NGAL 通过增强 MMP-9 的酶活性,成为甲状腺癌中核因子-κB 促转移活性的一个新靶点。