Voigt Heike, Vetter-Kauczok Claudia S, Schrama David, Hofmann Uta B, Becker Jürgen C, Houben Roland
Department of Dermatology, Julius-Maximilians-University, Würzburg, Germany.
Cancer Invest. 2009 Mar;27(3):329-33. doi: 10.1080/07357900802392675.
CD147 is highly expressed on many tumor cells; its role for tumor invasiveness and metastasis has been deduced from its capacity to induce MMPs, i.e., MMP-1, -2, -3, and -9. However, in the murine B16 melanoma model, MMP-2/-9 expression occurs independent of CD147. To scrutinize the impact of CD147 on metastasis formation and angiogenesis in this model, CD147 was stably knocked down in B16 cells. This silencing of CD147 expression resulted in a reduced capability of the tumor cells to metastasize to the draining lymph nodes. Notably, the CD147 knock down caused a decreased VEGF expression in vivo accompanied by reduced blood vessel formation. Thus, in the B16 melanoma model, CD147 promotes metastasis formation by induction of angiogenesis in an MMP independent manner.
CD147在许多肿瘤细胞上高表达;其对肿瘤侵袭和转移的作用已从其诱导基质金属蛋白酶(MMPs)的能力推导得出,即MMP - 1、- 2、- 3和- 9。然而,在小鼠B16黑色素瘤模型中,MMP - 2/- 9的表达独立于CD147。为了在该模型中仔细研究CD147对转移形成和血管生成的影响,CD147在B16细胞中被稳定敲低。CD147表达的这种沉默导致肿瘤细胞转移至引流淋巴结的能力降低。值得注意的是,CD147敲低导致体内VEGF表达降低,同时血管形成减少。因此,在B16黑色素瘤模型中,CD147通过以MMP非依赖的方式诱导血管生成来促进转移形成。