Department of Microbiology & Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, Canada.
Experimental Medicine Program, University of British Columbia, BC Children's Hospital, Vancouver, BC, Canada.
Cell Death Dis. 2018 Feb 7;9(2):162. doi: 10.1038/s41419-017-0194-1.
Proteasome inhibitors have emerged as an effective therapy for the treatment of haematological malignancies; however, their efficacy can be limited by the development of tumour resistance mechanisms. Novel combination strategies including the addition of TLR adjuvants to increase cell death and augment immune responses may help enhance their effectiveness. Although generally thought to inhibit inflammatory responses and NF-κB activation, we found that under specific conditions proteasome inhibitors can promote inflammatory responses by mediating IL-1β maturation and secretion after TLR stimulation. This was dependent on the timing of proteasome inhibition relative to TLR stimulation where reversal of treatment order could alternatively increase or inhibit IL-1β secretion (P < 0.001). TLR stimulation combined with proteasome inhibition enhanced cell death in vitro and delayed tumour development in vivo in NOD SCID mice (P < 0.01). However, unlike IL-1β secretion, cell death occurred similarly regardless of treatment order and was only partially caspase dependent, possessing characteristics of both apoptosis and necrosis as indicated by activation of caspase-1, 3, 8 and RIP3 phosphorylation. Although stimulation of various TLRs was capable of driving IL-1β production, TLR4 stimulation was the most effective at increasing cell death in THP-1 and U937 cells. TLR4 stimulation and proteasome inhibition independently activated the RIP3 necroptotic pathway and ultimately reduced the effectiveness of caspase/necroptosis inhibitors in mitigating overall levels of cell death. This strategy of combining TLR stimulation with proteasome inhibition may improve the ability of proteasome inhibitors to generate immunogenic cell death and increase anti-tumour activity.
蛋白酶体抑制剂已成为治疗血液系统恶性肿瘤的有效疗法;然而,肿瘤耐药机制的发展可能会限制其疗效。包括添加 TLR 佐剂以增加细胞死亡和增强免疫反应的新型联合策略可能有助于提高其疗效。尽管通常被认为抑制炎症反应和 NF-κB 激活,但我们发现,在特定条件下,蛋白酶体抑制剂可以通过介导 TLR 刺激后 IL-1β 的成熟和分泌来促进炎症反应。这取决于蛋白酶体抑制相对于 TLR 刺激的时间,治疗顺序的逆转可以替代地增加或抑制 IL-1β 的分泌(P < 0.001)。TLR 刺激联合蛋白酶体抑制可增强体外细胞死亡并延迟 NOD SCID 小鼠体内肿瘤发展(P < 0.01)。然而,与 IL-1β 分泌不同,细胞死亡的发生方式相似,无论治疗顺序如何,并且仅部分依赖于半胱天冬酶,如 caspase-1、3、8 和 RIP3 磷酸化的激活所表明的那样,具有凋亡和坏死的特征。虽然刺激各种 TLR 都能够驱动 IL-1β 的产生,但 TLR4 刺激在 THP-1 和 U937 细胞中最有效地增加细胞死亡。TLR4 刺激和蛋白酶体抑制独立激活 RIP3 坏死途径,最终降低 caspase/坏死抑制剂减轻细胞死亡总水平的效果。这种将 TLR 刺激与蛋白酶体抑制相结合的策略可能会提高蛋白酶体抑制剂产生免疫原性细胞死亡和增加抗肿瘤活性的能力。