Lucas Neali, Day Mark L
Department of Urology, University of Michigan, Ann Arbor, MI 48109-5944, USA.
J Cell Biochem. 2009 Apr 15;106(6):967-74. doi: 10.1002/jcb.22087.
The metalloproteinase ADAM15 is a multi-domain disintegrin protease that is upregulated in a variety of human cancers. ADAM15 mRNA and protein levels are increased in prostate cancer and its expression is significantly increased during metastatic progression. It is likely that ADAM15 supports disease progression differentially through the action of its various functional domains. ADAM15 may downregulate adhesion of tumor cells to the extracellular matrix, reduce cell-cell adhesion, and promote metastasis through the activity of its disintegrin and metalloproteinase domains. Additionally, ADAM15 can influence cell signaling by shedding membrane-bound growth factors and other proteins that interact with receptor tyrosine kinases, leading to receptor activation. There is also evidence supporting a role for ADAM15 in angiogenesis and angioinvasion of tumor cells, which are critical for unrestrained tumor growth and metastatic spread. Given its diverse functions, ADAM15 may represent a pivotal regulatory component of tumor progression, an important target for therapeutic intervention, or emerge as a biomarker of disease progression.
金属蛋白酶ADAM15是一种多结构域解整合素蛋白酶,在多种人类癌症中上调。ADAM15的mRNA和蛋白质水平在前列腺癌中升高,并且在转移进展过程中其表达显著增加。ADAM15可能通过其各种功能结构域的作用以不同方式支持疾病进展。ADAM15可能通过其解整合素和金属蛋白酶结构域的活性下调肿瘤细胞与细胞外基质的粘附,减少细胞间粘附,并促进转移。此外,ADAM15可以通过释放与受体酪氨酸激酶相互作用的膜结合生长因子和其他蛋白质来影响细胞信号传导,从而导致受体激活。也有证据支持ADAM15在肿瘤细胞的血管生成和血管侵袭中起作用,这对于不受限制的肿瘤生长和转移扩散至关重要。鉴于其多样的功能,ADAM15可能代表肿瘤进展的关键调节成分,是治疗干预的重要靶点,或者成为疾病进展的生物标志物。