Kim Joo-Young, Kim Young-Mi, Park Jong-Min, Han Young Min, Lee Kang Choon, Hahm Ki Baik, Hong Suntaek
Laboratory of Cancer Cell Biology, Department of Biochemistry, School of Medicine, Gachon University, Incheon, Korea.
CHA Cancer Prevention Research Center, CHA Cancer Institute, CHA University, Seongnam, Korea.
Oncotarget. 2017 Dec 7;9(2):1705-1716. doi: 10.18632/oncotarget.23083. eCollection 2018 Jan 5.
The potential of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) in inducing apoptosis is a hallmark in cancer therapeutics, after which its selective ability to achieve cell death pathways against cancer cells led to hope for recombinant TRAIL in cancer therapeutics. The present data from azoxymethane-initiated, dextran sulfate sodium-promoted colitis associated cancer (CAC) model strongly indicate the potential of rTRAIL in cancer prevention rather than in cancer therapeutics. Early treatment of rTRAIL significantly reduced colitis and CAC by inhibiting the recruitment of macrophages into the damaged mucosa and activating the scavenger activity with efferocytosis and the production of several growth factors. In contrast, late administration of rTRAIL as for anti-cancer effect did not decrease the initiation and development of CAC at all. Significant cancer preventing mechanisms of rTRAIL were identified. In the CAC model, anti-inflammation, regeneration, and efferocytosis was induced by treatment of TRAIL for 6 days, significant inhibitory activity was evident at 4 weeks and anti-oxidative and anti-inflammatory induction were noted at 12 weeks. Most importantly, TRAIL promoted tissue regeneration by enhancing the resolution of pathological inflammation through the activation of the NLRP3 inflammasome pathway. The results indicate that TRAIL reduces the induction of colitis and the initiation of CAC by inhibiting pro-inflammatory signaling and promoting tissue repair to maintain intestinal homeostasis through activation of the NLRP3 inflammasome. Therefore, TRAIL can be used as a chemopreventive agent against CAC, rather than as a therapeutic drug endowing apoptosis.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导细胞凋亡的潜力是癌症治疗的一个标志,此后其针对癌细胞实现细胞死亡途径的选择性能力为重组TRAIL在癌症治疗中带来了希望。来自氧化偶氮甲烷引发、葡聚糖硫酸钠促进的结肠炎相关癌症(CAC)模型的现有数据有力地表明,重组TRAIL在癌症预防而非癌症治疗方面具有潜力。重组TRAIL的早期治疗通过抑制巨噬细胞向受损黏膜的募集以及通过胞葬作用激活清除活性和几种生长因子的产生,显著减轻了结肠炎和CAC。相比之下,为达到抗癌效果而晚期给予重组TRAIL根本没有降低CAC的起始和发展。确定了重组TRAIL重要的癌症预防机制。在CAC模型中,TRAIL治疗6天可诱导抗炎、再生和胞葬作用,4周时明显有显著的抑制活性,12周时观察到抗氧化和抗炎诱导作用。最重要的是,TRAIL通过激活NLRP3炎性小体途径增强病理性炎症的消退,从而促进组织再生。结果表明,TRAIL通过抑制促炎信号传导和促进组织修复以通过激活NLRP3炎性小体维持肠道稳态,从而减少结肠炎的诱导和CAC的起始。因此,TRAIL可作为预防CAC的化学预防剂,而不是作为赋予细胞凋亡作用的治疗药物。