Woodward Alexis, Faria Gabriela N F, Harrison Roger G
Stephenson School of Biomedical Engineering, University of Oklahoma, Norman, OK, USA.
School of Chemical, Biological and Materials Engineering, University of Oklahoma, Norman, OK, USA.
Cancer Lett. 2022 Oct 28;547:215857. doi: 10.1016/j.canlet.2022.215857. Epub 2022 Aug 6.
Identifying a universal biomarker for cancer treatment remains a major challenge in cancer therapy. Extracellular exposure of phosphatidylserine (PS) is tightly regulated and is an "eat me" signal for phagocytosis in healthy cells. Although cancer cells and vasculature express high levels of externalized PS, they do not undergo apoptosis, making them a promising biomarker for cancer treatment. Annexin A5 (ANXA5) is the native binding partner of PS and can actively target and deliver chemotherapies to the tumor microenvironment (TME) via PS expression. ANXA5 acts as a bridge between the innate and adaptive immune systems and contributes to an immunostimulatory profile in the TME. ANXA5-enzyme prodrug therapies allow for systemic delivery of prodrugs and targeted killing at the tumor site. ANXA5-carbon nanotube conjugates have been used to physically ablate tumors via photothermal therapy. This review aims to explore the expression of PS in cancer cells and how ANXA5 has been used as a chemotherapeutic and targeting agent for cancer.
识别一种用于癌症治疗的通用生物标志物仍然是癌症治疗中的一项重大挑战。磷脂酰丝氨酸(PS)的细胞外暴露受到严格调控,并且是健康细胞中吞噬作用的“吃我”信号。尽管癌细胞和脉管系统表达高水平的外化PS,但它们不会发生凋亡,这使其成为癌症治疗中一个有前景的生物标志物。膜联蛋白A5(ANXA5)是PS的天然结合伴侣,并且可以通过PS表达将化疗药物主动靶向并递送至肿瘤微环境(TME)。ANXA5作为先天性和适应性免疫系统之间的桥梁,并有助于在TME中形成免疫刺激特征。ANXA5-酶前药疗法允许前药的全身递送以及在肿瘤部位的靶向杀伤。ANXA5-碳纳米管缀合物已被用于通过光热疗法物理消融肿瘤。本综述旨在探讨PS在癌细胞中的表达以及ANXA5如何被用作癌症的化疗和靶向药物。