Biomedical Research in Cancer Stem Cell Group, Pathology Department, Vall d'Hebron Hospital, 08035, Barcelona, Spain.
Otolaryngology Department, Vall d'Hebron Hospital, 08035, Barcelona, Spain.
Biol Rev Camb Philos Soc. 2018 Feb;93(1):152-165. doi: 10.1111/brv.12337. Epub 2017 May 2.
In wild-type cells, autophagy represents a tumour-suppressor mechanism, and dysfunction of the autophagy machinery increases genomic instability, DNA damage, oxidative stress and stem/progenitor expansion, which are events associated with cancer onset. Autophagy occurs at a basal level in all cells depending on cell type and cellular microenvironment. However, the role of autophagy in cancer is diverse and can promote different outcomes even in a single tumour. For example, in hypoxic tumour regions, autophagy emerges as a protective mechanism and allows cancer cell survival. By contrast, in cancer cells surrounding the tumour mass, the induction of autophagy by radio- or chemotherapy promotes cell death and significantly reduces the tumour mass. Importantly, inhibition of autophagy compromises tumorigenesis by mechanisms that are not entirely understood. The aim of this review is to explain the apparently contradictory role of autophagy as a mechanism that both promotes and inhibits tumorigenesis using different models. The induction/inhibition of autophagy as a mechanism for cancer treatment is also discussed.
在野生型细胞中,自噬代表一种肿瘤抑制机制,而自噬机制的功能障碍会增加基因组不稳定性、DNA 损伤、氧化应激和干细胞/祖细胞扩增,这些都是与癌症发生相关的事件。自噬在所有细胞中都以基础水平发生,具体取决于细胞类型和细胞微环境。然而,自噬在癌症中的作用是多样化的,即使在单个肿瘤中也可以促进不同的结果。例如,在缺氧的肿瘤区域,自噬会出现作为一种保护机制,允许癌细胞存活。相比之下,在肿瘤周围的癌细胞中,放射或化学疗法诱导的自噬会促进细胞死亡,并显著减少肿瘤体积。重要的是,自噬的抑制通过尚未完全理解的机制损害了肿瘤发生。本综述的目的是使用不同的模型解释自噬作为一种促进和抑制肿瘤发生的机制的明显矛盾作用。还讨论了自噬作为癌症治疗机制的诱导/抑制。