Wang Qiang, Greene Mark I
Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cancers (Basel). 2024 Apr 27;16(9):1705. doi: 10.3390/cancers16091705.
Survivin was initially identified as a member of the inhibitor apoptosis (IAP) protein family and has been shown to play a critical role in the regulation of apoptosis. More recent studies showed that survivin is a component of the chromosome passenger complex and acts as an essential mediator of mitotic progression. Other potential functions of survivin, such as mitochondrial function and autophagy, have also been proposed. Survivin has emerged as an attractive target for cancer therapy because its overexpression has been found in most human cancers and is frequently associated with chemotherapy resistance, recurrence, and poor survival rates in cancer patients. In this review, we discuss our current understanding of how survivin mediates various aspects of malignant transformation and drug resistance, as well as the efforts that have been made to develop therapeutics targeting survivin for the treatment of cancer.
生存素最初被鉴定为凋亡抑制蛋白(IAP)家族的成员,并已证明在细胞凋亡调节中起关键作用。最近的研究表明,生存素是染色体乘客复合体的一个组成部分,并作为有丝分裂进程的重要调节因子发挥作用。生存素的其他潜在功能,如线粒体功能和自噬,也已被提出。生存素已成为癌症治疗的一个有吸引力的靶点,因为在大多数人类癌症中都发现其过度表达,并且经常与化疗耐药、复发以及癌症患者的低生存率相关。在这篇综述中,我们讨论了目前对生存素如何介导恶性转化和耐药性各个方面的理解,以及为开发靶向生存素的癌症治疗药物所做的努力。