Boutin Jean A, Ferry Gilles
Pharmacologie Moléculaire et Cellulaire, Institut de Recherches SERVIER, Croissy-sur-Seine, France.
Cell Mol Life Sci. 2009 Sep;66(18):3009-21. doi: 10.1007/s00018-009-0056-9. Epub 2009 Jun 9.
Autotaxin is a protein of approximately 900 amino acids discovered in the early 1990s. Over the past 15 years, a strong association between cancer cells and autotaxin production has been observed. Recent publications indicate that autotaxin and the capacity of cancer to metastasise are intimately linked. The discovery of new molecular targets in pharmacology is a mixture of pure luck, hard work and industrial strategy. Despite a crucial and desperate need for new therapeutic tools, many targets are approached in oncology, but only a few are validated and end up at the patient bed. Outside the busy domain of kinases, few targets have been discovered that can be useful in treating cancer, particularly metastatic processes. The fortuitous relationship between autotaxin and lysophosphatidic acid renders the results of observations made in the diabetes/obesity context considerably important. The literature provides observations that may aid in redesigning experiments to validate autotaxin as a potential oncology target.
自分泌运动因子是一种在20世纪90年代初发现的由大约900个氨基酸组成的蛋白质。在过去15年里,人们观察到癌细胞与自分泌运动因子的产生之间存在紧密联系。最近的出版物表明,自分泌运动因子与癌症转移能力密切相关。药理学中新分子靶点的发现是纯粹运气、辛勤工作和产业策略的结合。尽管迫切需要新的治疗工具,但肿瘤学中有许多靶点被研究,但只有少数得到验证并最终应用于患者治疗。在激酶这个热门领域之外,很少发现可用于治疗癌症(特别是转移过程)的靶点。自分泌运动因子与溶血磷脂酸之间的偶然关系使得在糖尿病/肥胖背景下所做观察结果相当重要。文献提供的观察结果可能有助于重新设计实验,以验证自分泌运动因子作为潜在肿瘤学靶点的作用。