Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294-0017, USA.
Brain Pathol. 2012 Jan;22(1):89-98. doi: 10.1111/j.1750-3639.2011.00544.x.
The role of autophagy, traditionally considered a cellular homeostatic and recycling mechanism, has expanded dramatically to include an involvement in discrete stages of tumor initiation and development. Gliomas are the most aggressive and also the most common brain malignancies. Current treatment modalities have only a modest effect on patient outcomes. Resistance to apoptosis, a hallmark of most cancers, has driven the search for novel targets in cancer therapy. The autophagy lysosomal pathway is one such target that is being explored in multiple cancers including gliomas and is a promising avenue for further therapeutic development. This review summarizes our current understanding of the autophagic process and its potential utility as a target for glioma therapy.
自噬作用传统上被认为是一种细胞内稳态和回收机制,但其作用已经大大扩展,包括参与肿瘤发生和发展的各个阶段。神经胶质瘤是最具侵袭性的,也是最常见的脑恶性肿瘤。目前的治疗方式对患者的预后只有适度的影响。大多数癌症的一个标志是抗细胞凋亡,这促使人们在癌症治疗中寻找新的靶点。自噬溶酶体途径就是这样一个靶点,它正在包括神经胶质瘤在内的多种癌症中进行研究,是进一步治疗开发的一个有前途的途径。这篇综述总结了我们目前对自噬过程的理解及其作为神经胶质瘤治疗靶点的潜在用途。