UMRS, CRC, INSERM, Paris, France.
Cancer Lett. 2010 Sep 28;295(2):242-51. doi: 10.1016/j.canlet.2010.03.007. Epub 2010 Mar 31.
Matrix metalloproteinase-9 (MMP-9) strongly influences tumor development and metastasis. Using resistant (rMCF-7) and sensitive (sMCF-7) breast cancer lines we investigated the role of MMP-9 in cell migration (CM) and tubular network (TN) formation, two processes implied in tumor growth and metastasis. Our data demonstrate that MMP-9 which is critical for CM is necessary but not sufficient for TN formation and suggest a link between MDR1/P-gp and constitutive MMP-9. Both TN formation and CM are dependent on PKC and ERK1/2 pathways. This study reinforces the logic of combining therefore MMP inhibitors in cancer therapy, especially in patients with chemoresistance and invasion/metastasis.
基质金属蛋白酶-9(MMP-9)强烈影响肿瘤的发生和转移。我们使用耐药(rMCF-7)和敏感(sMCF-7)乳腺癌细胞系研究了 MMP-9 在细胞迁移(CM)和管状网络(TN)形成中的作用,这两个过程涉及肿瘤生长和转移。我们的数据表明,MMP-9 对于 CM 至关重要,但对于 TN 形成不是必需的,并且提示 MDR1/P-糖蛋白与组成型 MMP-9 之间存在联系。TN 形成和 CM 均依赖于 PKC 和 ERK1/2 途径。这项研究加强了在癌症治疗中联合使用 MMP 抑制剂的逻辑,特别是在化疗耐药和侵袭/转移的患者中。