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Metformin Treatment Inhibits Motility and Invasion of Glioblastoma Cancer Cells

机译:二甲双胍治疗抑制胶质母细胞瘤癌细胞的运动和侵袭

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摘要

Glioblastoma multiforme (GBM) is one of the most common and deadliest cancers of the central nervous system (CNS). GBMs high ability to infiltrate healthy brain tissues makes it difficult to remove surgically and account for its fatal outcomes. To improve the chances of survival, it is critical to screen for GBM-targeted anticancer agents with anti-invasive and antimigratory potential. Metformin, a commonly used drug for the treatment of diabetes, has recently emerged as a promising anticancer molecule. This prompted us, to investigate the anticancer potential of metformin against GBMs, specifically its effects on cell motility and invasion. The results show a significant decrease in the survival of SF268 cancer cells in response to treatment with metformin. Furthermore, metformin's efficiency in inhibiting 2D cell motility and cell invasion in addition to increasing cellular adhesion was also demonstrated in SF268 and U87 cells. Finally, AKT inactivation by downregulation of the phosphorylation level upon metformin treatment was also evidenced. In conclusion, this study provides insights into the anti-invasive antimetastatic potential of metformin as well as its underlying mechanism of action.
机译:多形胶质母细胞瘤(GBM)是中枢神经系统(CNS)最常见和最致命的癌症之一。 GBM渗透健康脑组织的高能力使其难以通过外科手术切除并导致其致命后果。为了提高生存机会,筛选具有抗侵袭和抗迁移潜力的靶向GBM的抗癌药物至关重要。二甲双胍是一种用于治疗糖尿病的常用药物,最近已成为一种有前途的抗癌分子。这促使我们研究二甲双胍对GBM的抗癌潜力,尤其是其对细胞运动和侵袭的影响。结果表明,响应二甲双胍治疗,SF268癌细胞的存活率显着降低。此外,在SF268和U87细胞中,除增加细胞粘附性外,还证实了二甲双胍在抑制2D细胞运动和细胞侵袭方面的效率。最后,还证实了通过二甲双胍治疗后磷酸化水平的下调而使AKT失活。总之,本研究提供了对二甲双胍抗侵袭性抗转移潜力及其潜在作用机制的见解。

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