Ludwig Ralf J, Schön Michael P, Boehncke Wolf-Henning
Johann Wolfgang Goethe University, Department of Dermatology, Theodor-Stern-Kai 7, Frankfurt am Main, Germany.
Expert Opin Ther Targets. 2007 Aug;11(8):1103-17. doi: 10.1517/14728222.11.8.1103.
P-selectin belongs to the family of selectin adhesion molecules, and is expressed by platelets and endothelial cells on stimulation. This pattern of expression may indicate an involvement of this molecule in inflammation and coagulation. Data from mice lacking P-selectin expression confirmed this assumption. In addition, a key role of P-selectin in the formation of tumour metastases has been established. Apparently unrelated, clinical experience has pointed towards a detrimental interaction of inflammation and cancer with thromboembolic diseases and vice versa. Therefore, targeting molecules such as P-selectin contributing to coagulation, inflammation and metastasis may offer novel therapeutic strategies to treat chronic inflammatory diseases and metastatic cancer. The authors aim to critically evaluate the contribution of P-selectin in these diseases, and discuss the value of therapeutic inhibition of P-selectin functions in coagulation, inflammation and metastasis.
P选择素属于选择素黏附分子家族,在受到刺激时由血小板和内皮细胞表达。这种表达模式可能表明该分子参与了炎症和凝血过程。缺乏P选择素表达的小鼠的数据证实了这一假设。此外,P选择素在肿瘤转移形成中的关键作用也已得到确立。表面上不相关的临床经验表明,炎症和癌症与血栓栓塞性疾病之间存在有害的相互作用,反之亦然。因此,靶向诸如P选择素这类有助于凝血、炎症和转移的分子,可能会提供治疗慢性炎症性疾病和转移性癌症的新治疗策略。作者旨在批判性地评估P选择素在这些疾病中的作用,并讨论在凝血、炎症和转移过程中对P选择素功能进行治疗性抑制的价值。