Gupta Gourab, Borglum Kristina, Chen Hexin
Department of Biological Science, Center for Colon Cancer Research, University of South Carolina, Columbia, SC 29208, USA.
J Cancer Immunol (Wilmington). 2021;3(1):47-59. doi: 10.33696/cancerimmunol.3.041.
Immunogenic cell death (ICD) plays a major role in providing long lasting protective antitumor immunity by the chronic exposure of damage associated molecular patterns (DAMPs) in the tumor microenvironment (TME). DAMPs are essential for attracting immunogenic cells to the TME, maturation of DCs, and proper presentation of tumor antigens to the T cells so they can kill more cancer cells. Thus for the proper release of DAMPs, a controlled mechanism of cell death is necessary. Drug induced tumor cell killing occurs by apoptosis, wherein autophagy may act as a shield protecting the tumor cells and sometimes providing multi-drug resistance to chemotherapeutics. However, autophagy is required for the release of ATP as it remains one of the key DAMPs for the induction of ICD. In this review, we discuss the intricate balance between autophagy and apoptosis and the various strategies that we can apply to make these immunologically silent processes immunogenic. There are several steps of autophagy and apoptosis that can be regulated to generate an immune response. The genes involved in the processes can be regulated by drugs or inhibitors to amplify the effects of ICD and therefore serve as potential therapeutic targets.
免疫原性细胞死亡(ICD)通过在肿瘤微环境(TME)中长期暴露损伤相关分子模式(DAMPs),在提供持久的保护性抗肿瘤免疫方面发挥主要作用。DAMPs对于吸引免疫原性细胞至TME、树突状细胞(DC)的成熟以及将肿瘤抗原正确呈递给T细胞从而使其能够杀伤更多癌细胞至关重要。因此,为了DAMPs的正确释放,一种可控的细胞死亡机制是必要的。药物诱导的肿瘤细胞杀伤通过凋亡发生,其中自噬可能充当保护肿瘤细胞的屏障,有时还会赋予对化疗药物的多药耐药性。然而,自噬对于ATP的释放是必需的,因为ATP仍然是诱导ICD的关键DAMPs之一。在本综述中,我们讨论了自噬与凋亡之间的复杂平衡以及我们可以应用的各种策略,以使这些免疫沉默过程具有免疫原性。自噬和凋亡的几个步骤可以被调控以产生免疫反应。参与这些过程的基因可以通过药物或抑制剂进行调控,以放大ICD的效应,因此可作为潜在的治疗靶点。