Guang Matthew Ho Zhi, Kavanagh Emma L, Dunne Luke Paul, Dowling Paul, Zhang Li, Lindsay Sinéad, Bazou Despina, Goh Chia Yin, Hanley Cathal, Bianchi Giada, Anderson Kenneth C, O'Gorman Peter, McCann Amanda
UCD Conway Institute of Biomolecular and Biomedical Science, Dublin, Dublin 4, Ireland.
UCD School of Medicine, College of Health and Agricultural Sciences, University College Dublin, Belfield Dublin, Dublin 4, Ireland.
Cancers (Basel). 2019 Jan 9;11(1):66. doi: 10.3390/cancers11010066.
Despite significant advances in cancer diagnostics and therapeutics the majority of cancer unfortunately remains incurable, which has led to continued research to better understand its exceptionally diverse biology. As a result of genomic instability, cancer cells typically have elevated proteotoxic stress. Recent appreciation of this functional link between the two secondary hallmarks of cancer: aneuploidy (oxidative stress) and proteotoxic stress, has therefore led to the development of new anticancer therapies targeting this emerging "Achilles heel" of malignancy. This review highlights the importance of managing proteotoxic stress for cancer cell survival and provides an overview of the integral role proteostasis pathways play in the maintenance of protein homeostasis. We further review the efforts undertaken to exploit proteotoxic stress in multiple myeloma (as an example of a hematologic malignancy) and triple negative breast cancer (as an example of a solid tumor), and give examples of: (1) FDA-approved therapies in routine clinical use; and (2) promising therapies currently in clinical trials. Finally, we provide new insights gleaned from the use of emerging technologies to disrupt the protein secretory pathway and repurpose E3 ligases to achieve targeted protein degradation.
尽管癌症诊断和治疗取得了重大进展,但不幸的是,大多数癌症仍然无法治愈,这促使人们持续开展研究,以更好地了解其异常多样的生物学特性。由于基因组不稳定,癌细胞通常具有更高的蛋白毒性应激。最近对癌症的两个次要特征——非整倍体(氧化应激)和蛋白毒性应激之间功能联系的认识,因此催生了针对这种恶性肿瘤新出现的“阿喀琉斯之踵”的新型抗癌疗法。本综述强调了管理蛋白毒性应激对癌细胞存活的重要性,并概述了蛋白质稳态途径在维持蛋白质平衡中所起的不可或缺的作用。我们进一步回顾了在多发性骨髓瘤(作为血液系统恶性肿瘤的一个例子)和三阴性乳腺癌(作为实体瘤的一个例子)中利用蛋白毒性应激所做的努力,并给出以下方面的例子:(1)常规临床使用的美国食品药品监督管理局(FDA)批准的疗法;(2)目前正在进行临床试验的有前景的疗法。最后,我们提供了从使用新兴技术破坏蛋白质分泌途径和重新利用E3连接酶以实现靶向蛋白质降解中获得的新见解。