Denicolaï Emilie, Baeza-Kallee Nathalie, Tchoghandjian Aurélie, Carré Manon, Colin Carole, Jiglaire Carine Jiguet, Mercurio Sandy, Beclin Christophe, Figarella-Branger Dominique
Inserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
CNRS, IBDML, Aix Marseille Université, UMR_S 6216, Marseille, 13288, France.
Oncotarget. 2014 Nov 15;5(21):10934-48. doi: 10.18632/oncotarget.2541.
Glioblastoma is the most frequent primary brain tumor in adults. Because of molecular and cellular heterogeneity, high proliferation rate and significant invasive ability, prognosis of patients is poor. Recent therapeutic advances increased median overall survival but tumor recurrence remains inevitable. In this context, we used a high throughput screening approach to bring out novel compounds with anti-proliferative and anti-migratory properties for glioblastoma treatment. Screening of the Prestwick chemical library® of 1120 molecules identified proscillaridin A, a cardiac glycoside inhibitor of the Na(+)/K(+) ATPase pump, with most significant effects on glioblastoma cell lines. In vitro effects of proscillaridin A were evaluated on GBM6 and GBM9 stem-like cell lines and on U87-MG and U251-MG cell lines. We showed that proscillaridin A displayed cytotoxic properties, triggered cell death, induced G2/M phase blockade in all the glioblastoma cell lines and impaired GBM stem self-renewal capacity even at low concentrations. Heterotopic and orthotopic xenotransplantations were used to confirm in vivo anticancer effects of proscillaridin A that both controls xenograft growth and improves mice survival. Altogether, results suggest that proscillaridin A is a promising candidate as cancer therapies in glioblastoma. This sustains previous reports showing that cardiac glycosides act as anticancer drugs in other cancers.
胶质母细胞瘤是成人中最常见的原发性脑肿瘤。由于其分子和细胞的异质性、高增殖率以及显著的侵袭能力,患者的预后较差。尽管近期治疗取得了进展,提高了总体中位生存期,但肿瘤复发仍然不可避免。在此背景下,我们采用高通量筛选方法来找出具有抗增殖和抗迁移特性的新型化合物用于胶质母细胞瘤治疗。对包含1120种分子的普瑞思威克化学文库进行筛选,确定了海葱苷A,一种钠钾ATP酶泵的强心苷抑制剂,对胶质母细胞瘤细胞系有最显著的影响。评估了海葱苷A对GBM6和GBM9干细胞样细胞系以及U87-MG和U251-MG细胞系的体外作用。我们发现海葱苷A具有细胞毒性,可引发细胞死亡,在所有胶质母细胞瘤细胞系中诱导G2/M期阻滞,甚至在低浓度下也能损害胶质母细胞瘤干细胞的自我更新能力。采用异位和原位异种移植来证实海葱苷A的体内抗癌作用,它既能控制异种移植瘤的生长,又能提高小鼠的生存率。总之,结果表明海葱苷A有望成为胶质母细胞瘤的癌症治疗候选药物。这支持了先前的报道,即强心苷在其他癌症中可作为抗癌药物。