Pasco Sylvie, Brassart Bertrand, Ramont Laurent, Maquart François-Xavier, Monboisse Jean-Claude
Laboratoire de Biochimie, UMR 6198 CNRS, IFR 53 Biomolecules, UFR Médecine, Université de Reims Champagne-Ardenne, 51 Rue Cognacq Jay, F51095, REIMS Cedex, France.
Cancer Detect Prev. 2005;29(3):260-6. doi: 10.1016/j.cdp.2004.09.003. Epub 2004 Nov 23.
Malignant melanoma is the leading cause of death from diseases of the skin. This review summarizes the data from the literature and our laboratory addressing the effects of type IV collagen on melanoma progression. Many different sequences from type IV collagen promote melanoma cell adhesion, migration and invasion. The triple helical conformation of the collagenous domain plays a critical role in some of these interactions. However, recent studies from our group demonstrated that a sequence from the alpha3(IV) NC1 domain inhibits melanoma cell proliferation, migration and invasion by decreasing MMP production and activation. Peptide sequences from the alpha1(IV), alpha2(IV) and alpha3(IV) chains named arresten, canstatin and tumstatin, respectively were shown to inhibit angiogenesis. Further investigations regarding the inhibitory effects of the alpha(IV) NC1 domains will have a paramount relevance for the design of efficient strategies to limit melanoma development.
恶性黑色素瘤是皮肤疾病致死的主要原因。本综述总结了文献及我们实验室关于IV型胶原对黑色素瘤进展影响的数据。IV型胶原的许多不同序列可促进黑色素瘤细胞的黏附、迁移和侵袭。胶原结构域的三螺旋构象在其中一些相互作用中起关键作用。然而,我们团队最近的研究表明,α3(IV) NC1结构域的一个序列可通过减少基质金属蛋白酶(MMP)的产生和激活来抑制黑色素瘤细胞的增殖、迁移和侵袭。分别来自α1(IV)、α2(IV)和α3(IV)链的肽序列,即抑制素、制癌素和tumstatin,已被证明可抑制血管生成。关于α(IV) NC1结构域抑制作用的进一步研究对于设计限制黑色素瘤发展的有效策略至关重要。