Yao R, Davidson D D, Lopez-Beltran A, MacLennan G T, Montironi R, Cheng L
Department of Surgery and The Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Histol Histopathol. 2007 Sep;22(9):1025-32. doi: 10.14670/HH-22.1025.
The S100 gene family, which is composed of at least 24 members carrying the Ca2+ binding EF-hand motif, has been implicated in both intracellular and extracellular functions, including enzyme activities, immune responses, cytoskeleton dynamics, Ca2+ homeostasis, cell growth and cell differentiation. Altered S100 protein levels are associated with a broad range of diseases, including cardiomyopathy, inflammatory and immune disorders, neurodegenerative disorders and cancer. Although the precise role of S100 protein in carcinogenesis is poorly understood, it seems that formation of homo- and hetero-dimers, binding of Ca2+ and interaction with effector molecules are essential for the development and progression of many cancers. Several studies have suggested that S100 proteins promote cancer progression and metastasis through cell survival and apoptosis pathways. In animal models of bladder cancer, several S100 proteins are differentially expressed in bladder tumors relative to normal urothelium. In human bladder cancer, overexpression of S100A4, S100A8 or S100A11 are associated with stage progression, invasion, metastasis and poor survival. This review summarizes these findings and evaluates their implications for human bladder cancer management.
S100基因家族由至少24个携带Ca2+结合EF手基序的成员组成,涉及细胞内和细胞外多种功能,包括酶活性、免疫反应、细胞骨架动力学、Ca2+稳态、细胞生长和细胞分化。S100蛋白水平的改变与多种疾病相关,包括心肌病、炎症和免疫紊乱、神经退行性疾病以及癌症。尽管S100蛋白在致癌作用中的确切作用尚不清楚,但同二聚体和异二聚体的形成、Ca2+的结合以及与效应分子的相互作用似乎对许多癌症的发生和发展至关重要。多项研究表明,S100蛋白通过细胞存活和凋亡途径促进癌症进展和转移。在膀胱癌动物模型中,相对于正常尿路上皮,几种S100蛋白在膀胱肿瘤中差异表达。在人类膀胱癌中,S100A4、S100A8或S100A11的过表达与分期进展、侵袭、转移及不良预后相关。本综述总结了这些发现,并评估了它们对人类膀胱癌管理的意义。