Um Hong-Duck
Division of Radiation Cancer Biology, Korea Institute of Radiological & Medical Sciences, Seoul, Korea.
Oncotarget. 2016 Feb 2;7(5):5193-203. doi: 10.18632/oncotarget.6405.
Although Bcl-2 family proteins were originally identified as key regulators of apoptosis, an impressive body of evidence has shown that pro-survival members of the Bcl-2 family, including Bcl-2, Bcl-XL, and Bcl-w, can also promote cell migration, invasion, and cancer metastasis. Interestingly, cell invasion was recently found to be suppressed by multidomain pro-apoptotic members of the Bcl-2 family, such as Bax and Bak. While the mechanisms underlying these new functions of Bcl-2 proteins are just beginning to be studied, reactive oxygen species (ROS) have emerged as inducers of cell invasion and the production of ROS from mitochondrial respiration is known to be promoted and suppressed by the pro-survival and multidomain pro-apoptotic Bcl-2 family members, respectively. Here, I review the evidence supporting the ability of Bcl-2 proteins to regulate cancer cell invasion and metastasis, and discuss our current understanding of their underlying mechanisms, with a particular focus on mitochondrial respiration and ROS, which could have implications for the development of strategies to overcome tumor progression.
虽然Bcl-2家族蛋白最初被鉴定为细胞凋亡的关键调节因子,但大量证据表明,Bcl-2家族的促生存成员,包括Bcl-2、Bcl-XL和Bcl-w,也能促进细胞迁移、侵袭和癌症转移。有趣的是,最近发现Bcl-2家族的多结构域促凋亡成员,如Bax和Bak,可抑制细胞侵袭。虽然Bcl-2蛋白这些新功能的潜在机制才刚刚开始研究,但活性氧(ROS)已成为细胞侵袭的诱导剂,并且已知线粒体呼吸产生的ROS分别受到促生存和多结构域促凋亡Bcl-2家族成员的促进和抑制。在此,我综述了支持Bcl-2蛋白调节癌细胞侵袭和转移能力的证据,并讨论了我们目前对其潜在机制的理解,特别关注线粒体呼吸和ROS,这可能对开发克服肿瘤进展的策略具有启示意义。