Huber-Villaume Sophie, Revelant Germain, Sibille Estelle, Philippot Stéphanie, Morabito Angelica, Dunand Sandrine, Chaimbault Patrick, Bagrel Denyse, Kirsch Gilbert, Hesse Stéphanie, Schohn Hervé
Université de Lorraine, UMR CNRS 7565, Structure et Réactivité des Systèmes Moléculaires Complexes, Equipe 5 (MIC), Campus Bridoux, rue du Général Delestraint, 57070 Metz Cedex, France.
Université de Lorraine, UMR CNRS 7565, Structure et Réactivité des Systèmes Moléculaires Complexes, Equipe 3 (HECRIN), 1 Boulevard Arago, 57078 Metz Technopôle, France.
Bioorg Med Chem. 2016 Jul 1;24(13):2920-2928. doi: 10.1016/j.bmc.2016.04.063. Epub 2016 May 2.
Cell division cycle dual phosphatases (CDC25) are essential enzymes that regulate cell progression in cell cycle. Three isoforms exist as CDC25A, B and C. Over-expression of each CDC25 enzyme is found in cancers of diverse origins. Thiazolidinone derivatives have been reported to display anti-proliferative activities, bactericidal activities and to reduce inflammation process. New 2-(thienothiazolylimino)-1,3-thiazolidin-4-ones were synthesized and evaluated as inhibitors of CDC25 phosphatase. Among the molecules tested, compound 6 inhibited CDC25A with an IC50 estimated at 6.2±1.0μM. The binding of thiazolidinone derivative 6 onto CDC25A protein was reversible. In cellulo, compound 6 treatment led to MCF7 and MDA-MB-231 cell growth arrest. To our knowledge, it is the first time that such 4-thiazolidinone derivatives are characterized as CDC25 potential inhibitor.
细胞分裂周期双磷酸酶(CDC25)是调节细胞周期中细胞进程的关键酶。它有三种同工型,即CDC25A、B和C。在多种起源的癌症中均发现每种CDC25酶的过表达。据报道,噻唑烷酮衍生物具有抗增殖活性、杀菌活性并能减轻炎症过程。合成了新型2-(噻吩并噻唑基亚氨基)-1,3-噻唑烷-4-酮,并将其作为CDC25磷酸酶的抑制剂进行评估。在所测试的分子中,化合物6对CDC25A的抑制作用的IC50估计为6.2±1.0μM。噻唑烷酮衍生物6与CDC25A蛋白的结合是可逆的。在细胞内,化合物6处理导致MCF7和MDA-MB-231细胞生长停滞。据我们所知,此类4-噻唑烷酮衍生物首次被表征为CDC25潜在抑制剂。