Kalkan Rasime
Department of Medical Genetics, Faculty of Medicine, Near East University, Post Code: 99138, Turkish Republic of Northern Cyprus.
Crit Rev Eukaryot Gene Expr. 2015;25(4):281-5. doi: 10.1615/critreveukaryotgeneexpr.2015014259.
Glioblastoma multiforme (GBM) is divided into two distinct disease entities called primary and secondary GBM. The genetic and the epigenetic background of these tumors are highly variable. These tumors are not successfully treated because of their cellular heterogeneity and intrinsic ability of the tumor cells to invade healthy tissues. The fatal outcomes of these tumors promote researchers to find new markers associated with prognosis and treatment planning. A better understanding of stem-like cells and the genetic and the epigenetic background of GBM are necessary for designing new effective treatments and developing novel molecular strategies to target tumor cells and glioblastoma stem cells. In this review, we discuss the new therapeutic targets. Focusing on inhibiting the signaling pathways, which are associated with hypoxia-mediated maintenance of glioblastoma stem cells or the knockdown of the hypoxia-inducible factor 1-alpha (HIF1α), may help to the develop new target-specific treatments.
多形性胶质母细胞瘤(GBM)分为原发性和继发性GBM这两种不同的疾病实体。这些肿瘤的遗传和表观遗传背景高度可变。由于其细胞异质性以及肿瘤细胞侵袭健康组织的内在能力,这些肿瘤尚未得到成功治疗。这些肿瘤的致命后果促使研究人员寻找与预后和治疗规划相关的新标志物。为了设计新的有效治疗方法并开发针对肿瘤细胞和胶质母细胞瘤干细胞的新型分子策略,深入了解干细胞样细胞以及GBM的遗传和表观遗传背景是必要的。在本综述中,我们讨论了新的治疗靶点。专注于抑制与缺氧介导的胶质母细胞瘤干细胞维持相关的信号通路或敲低缺氧诱导因子1α(HIF1α),可能有助于开发新的靶向特异性治疗方法。