University Claude Bernard Lyon 1, Lyon, France.
J Natl Cancer Inst. 2013 Jul 3;105(13):937-46. doi: 10.1093/jnci/djt120. Epub 2013 Jun 13.
MyD88 is an adaptor molecule in Toll-like receptor and interleukin 1 receptor signaling implicated in tumorigenesis through proinflammatory mechanisms. We have recently reported that MyD88 also directly promotes optimal activation of the Ras/Erk pathway. Here we investigate MyD88 implication in the maintenance of the transformation of Ras-dependent tumors.
RNA interference was used to inhibit MyD88 expression in the colon cancer cell lines HCT116 and LS513. Apoptosis, DNA damage, p53 function, ERCC1 levels, and Ras and inflammatory signaling pathways were analyzed. Using in vitro assays and xenotransplantation in nude mice (five per group), HCT116 tumor growth was assessed following MyD88 knockdown in presence or absence of chemotherapy.
MyD88 exerts antiapoptotic functions in colon cancer cells via the Ras/Erk, but not the NF-κB, pathway. MyD88 inhibition leads to defective ERCC1-dependent DNA repair and to accumulation of DNA damage, resulting in cancer cell death via p53. Furthermore, we show that knocking down MyD88 sensitizes cancer cells to genotoxic agents such as platinum salts in vitro and in vivo. Indeed, HCT116 tumor growth following treatment with a combination of suboptimal MyD88 inhibition and suboptimal doses of cisplatin (fold tumor increase = 5.4 ± 1.6) was statistically significantly reduced in comparison to treatment with doxycycline alone (12.4 ± 3.1) or with cisplatin alone (12.5 ± 2.6) (P = .005 for both, one-sided Student t test).
Collectively, these results indicate a novel and original link between inflammation, DNA repair, and cancer, and provide further rationale for MyD88 as a potential therapeutic target in Ras-dependent cancers, in the context of concomitant genotoxic chemotherapy.
MyD88 是 Toll 样受体和白细胞介素 1 受体信号转导中的衔接分子,通过炎症机制参与肿瘤发生。我们最近报道 MyD88 还直接促进 Ras/Erk 通路的最佳激活。在这里,我们研究了 MyD88 对 Ras 依赖性肿瘤转化的维持作用。
使用 RNA 干扰抑制结肠癌细胞系 HCT116 和 LS513 中的 MyD88 表达。分析细胞凋亡、DNA 损伤、p53 功能、ERCC1 水平以及 Ras 和炎症信号通路。通过体外测定和裸鼠异种移植(每组 5 只),在存在或不存在化疗的情况下评估 HCT116 肿瘤生长。
MyD88 通过 Ras/Erk 而不是 NF-κB 途径在结肠癌细胞中发挥抗凋亡作用。MyD88 抑制导致 ERCC1 依赖性 DNA 修复缺陷和 DNA 损伤积累,导致 p53 依赖性癌细胞死亡。此外,我们表明,敲低 MyD88 可使癌细胞对体外和体内的遗传毒性药物(如顺铂)敏感。事实上,与单独使用多西环素(肿瘤增加倍数=5.4±1.6)或单独使用顺铂(肿瘤增加倍数=12.4±2.6)相比,用亚最佳 MyD88 抑制和亚最佳剂量顺铂联合治疗后 HCT116 肿瘤生长明显减少(P 值分别为 0.005,单侧学生 t 检验)。
总之,这些结果表明炎症、DNA 修复和癌症之间存在新的和原始的联系,并为 MyD88 作为 Ras 依赖性癌症中潜在的治疗靶点提供了进一步的依据,特别是在联合遗传毒性化疗的情况下。