Cui Jian-Zhou, Chew Zhi Huan, Lim Lina H K
Translational Immunology Program, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; NUS Immunology Program, Life Sciences Institute, National University of Singapore, Singapore; NUS-Cambridge Immunophenotyping Centre, Life Science Institute, National University of Singapore, Singapore.
Translational Immunology Program, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; NUS Immunology Program, Life Sciences Institute, National University of Singapore, Singapore; NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore; Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Pharmacol Res. 2024 Feb;200:107079. doi: 10.1016/j.phrs.2024.107079. Epub 2024 Jan 24.
The AIM2 inflammasome represents a multifaceted oligomeric protein complex within the innate immune system, with the capacity to perceive double-stranded DNA (dsDNA) and engage in diverse physiological reactions and disease contexts, including cancer. While originally conceived as a discerning DNA sensor, AIM2 has demonstrated its capability to discern various nucleic acid variations, encompassing RNA and DNA-RNA hybrids. Through its interaction with nucleic acids, AIM2 orchestrates the assembly of a complex involving multiple proteins, aptly named the AIM2 inflammasome, which facilitates the enzymatic cleavage of proinflammatory cytokines, namely pro-IL-1β and pro-IL-18. This process, in turn, underpins its pivotal biological role. In this review, we provide a systematic summary and discussion of the latest advancements in AIM2 sensing various types of nucleic acids. Additionally, we discuss the modulation of AIM2 activation, which can cause cell death, including pyroptosis, apoptosis, and autophagic cell death. Finally, we fully illustrate the evidence for the dual role of AIM2 in different cancer types, including both anti-tumorigenic and pro-tumorigenic functions. Considering the above information, we uncover the therapeutic promise of modulating the AIM2 inflammasome in cancer treatment.
AIM2炎性小体是先天性免疫系统中一种多面性的寡聚蛋白复合物,能够识别双链DNA(dsDNA),并参与包括癌症在内的多种生理反应和疾病情况。虽然AIM2最初被认为是一种识别DNA的传感器,但它已证明能够识别各种核酸变异,包括RNA和DNA-RNA杂交体。通过与核酸相互作用,AIM2协调了一个涉及多种蛋白质的复合物的组装,该复合物被恰当地命名为AIM2炎性小体,它促进促炎细胞因子(即前白细胞介素-1β和前白细胞介素-18)的酶促裂解。反过来,这一过程支撑了其关键的生物学作用。在这篇综述中,我们对AIM2识别各种类型核酸的最新进展进行了系统总结和讨论。此外,我们还讨论了AIM2激活所导致的细胞死亡的调节,包括细胞焦亡、凋亡和自噬性细胞死亡。最后,我们充分阐述了AIM2在不同癌症类型中双重作用的证据,包括抗肿瘤和促肿瘤功能。考虑到上述信息,我们揭示了调节AIM2炎性小体在癌症治疗中的治疗前景。