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机构地区:[1]中国医科大学基础医学院生物化学与分子生物学教研室,沈阳110001
出 处:《中国生物化学与分子生物学报》2014年第10期949-956,共8页Chinese Journal of Biochemistry and Molecular Biology
基 金:国家自然科学基金(No.81070489,No.81270654)资助项目~~
摘 要:哺乳动物雷帕霉素靶(mTOR)和蛋白激酶B(Akt/PKB)与肿瘤发生的密切关系已被广泛地认可.mTOR是一种丝/苏氨酸激酶,可以通过影响mRNA转录、代谢、自噬等方式调控细胞的生长.它既是PI3K的效应分子,也可以是PI3K的反馈调控因子.mTORC1和mTORC2是mTOR的两种不同复合物.对雷帕霉素敏感的mTORC1受到营养、生长因子、能量和应激4种因素的影响.生长因子通过PI3K/Akt信号通路调控mTORC1是最具特征性调节路径.而mTORC2最为人熟知的是作为Akt473磷酸化位点的上游激酶.同样,Akt/PKB在细胞增殖分化、迁移生长过程中发挥着重要作用.随着Thr308和Ser473两个位点激活,Akt/PKB也得以全面活化.因此,mTORC2-AktmTORC1的信号通路在肿瘤形成和生长中是可以存在的.目前临床肿瘤治疗中,PI3K/Akt/mTOR是重要的靶向治疗信号通路.然而,仅抑制mTORC1活性,不是所有的肿瘤都能得到预期控制.雷帕霉素虽然能抑制mTORC1,但也能反馈性地增加PI3K信号活跃度,从而影响治疗预后.近来发现的第二代抑制剂可以同时抑制mTORC1/2和PI3K活性,这种抑制剂被认为在肿瘤治疗上颇具前景.本综述着重阐述了PI3K/Akt/mTOR信号通路的传导、各因子之间的相互调控以及相关抑制剂的发展.The mammalian target of rapamycin (mTOR) and Akt/PKB (protein kinase B) are closely related to cancers. As a downstream effector and regulator of PI3K, the roTOR molecule regulates mRNA translation, metabolism and autophagy to affect cell growth. There are two types of mTOR multi protein complexes: mTORC1 and mTORC2. The former is sensitive to rapamycin and acts to respond to four major regulatory stimulations of nutrients, growth factors, energy and stress. The growth factor/PI3K/Akt pathway is the most identified signaling pathway for which to regulate. The latter is characterized as a kinase to phosphorylate Akt at Ser473, and then regulate cell growth/proliferatlon, motility, survival, and differentiation, especially when coordinated with Thr308 of Akt. The PI3K/Akt/mTOR pathway is an important therapeutic target of cancer treatments for its critical role in cancer cells. However, the first generation mTORCl-specific inhibitors of rapamycin analogs showed limited efficacy, probably due to the feedback activation of upstream PI3K signaling. Recently, the second generation inhibitors acted on both of mTORC1/2 and PI3K, which can be more promising in cancer treatment. This review describes recent reports on such novel inhibitors and their functions in the PI3K/Akt/mTOR signaling pathway.
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