Université de Reims Champagne-Ardenne, 51095 Reims, France.
Eur J Dermatol. 2010 Nov-Dec;20(6):712-8. doi: 10.1684/ejd.2010.1070. Epub 2010 Sep 14.
Type XIX collagen is a minor collagen that localizes to basement membrane zones. We previously demonstrated that the C-terminal NC1 domain of type XIX collagen inhibits tumor growth in vivo. In the present study, we analyzed the effects of the NC1(XIX) collagen domain on migratory behaviour of melanoma B16F10 cells. We found that NC1(XIX) do not inhibit melanoma cell proliferation. On the contrary, NC1(XIX) strongly inhibited the migratory capacities of melanoma cells in the scratch wound model and in Ibidi® devices: cell migration speed was 7.69 ± 1.49 μm/h for the controls vs 6.64 ± 0.82 μm/h for cells incubated with 30 μmol/L NC1(XIX) and 5.72 ± 0.67 μmol/h with 60 μmol/L NC1(XIX). Similar results were obtained with UACC 903 human melanoma cells. Further work will be necessary to elucidate the molecular mechanisms of this migration inhibition. It may, however, explain, at least partially, the inhibition of tumor growth that we observed in vivo.
XIX 型胶原是一种定位于基底膜区的次要胶原。我们之前证明,XIX 型胶原的 C 端 NC1 结构域在体内抑制肿瘤生长。在本研究中,我们分析了 NC1(XIX)胶原结构域对黑色素瘤 B16F10 细胞迁移行为的影响。我们发现,NC1(XIX)不会抑制黑色素瘤细胞的增殖。相反,NC1(XIX)强烈抑制划痕模型和 Ibidi®装置中黑色素瘤细胞的迁移能力:对照组的细胞迁移速度为 7.69±1.49μm/h,而用 30μmol/L NC1(XIX)孵育的细胞迁移速度为 6.64±0.82μm/h,用 60μmol/L NC1(XIX)孵育的细胞迁移速度为 5.72±0.67μm/h。UACC 903 人黑色素瘤细胞也得到了类似的结果。进一步的研究将需要阐明这种迁移抑制的分子机制。然而,它可能至少部分解释了我们在体内观察到的肿瘤生长抑制。