Chemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Nat Rev Cancer. 2018 Sep;18(9):562-575. doi: 10.1038/s41568-018-0020-9.
In this Opinion article, we aim to address how cells adapt to stress and the repercussions chronic stress has on cellular function. We consider acute and chronic stress-induced changes at the cellular level, with a focus on a regulator of cellular stress, the chaperome, which is a protein assembly that encompasses molecular chaperones, co-chaperones and other co-factors. We discuss how the chaperome takes on distinct functions under conditions of stress that are executed in ways that differ from the one-on-one cyclic, dynamic functions exhibited by distinct molecular chaperones. We argue that through the formation of multimeric stable chaperome complexes, a state of chaperome hyperconnectivity, or networking, is gained. The role of these chaperome networks is to act as multimolecular scaffolds, a particularly important function in cancer, where they increase the efficacy and functional diversity of several cellular processes. We predict that these concepts will change how we develop and implement drugs targeting the chaperome to treat cancer.
在这篇观点文章中,我们旨在探讨细胞如何适应压力,以及慢性压力对细胞功能的影响。我们考虑了细胞水平上的急性和慢性应激诱导的变化,重点关注细胞应激的调节剂——伴侣体,它是一个包含分子伴侣、共伴侣和其他辅助因子的蛋白质组装体。我们讨论了伴侣体在应激条件下如何承担不同的功能,其执行方式与不同分子伴侣所表现出的一对一循环、动态功能不同。我们认为,通过形成多聚体稳定的伴侣体复合物,可以获得伴侣体超连接或网络的状态。这些伴侣体网络的作用是作为多分子支架,在癌症中这是一个特别重要的功能,因为它们增加了几个细胞过程的效率和功能多样性。我们预测,这些概念将改变我们开发和实施靶向伴侣体治疗癌症的药物的方式。