Department of Molecular Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Medical Genomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Nat Cell Biol. 2020 Apr;22(4):465-475. doi: 10.1038/s41556-020-0491-2. Epub 2020 Mar 23.
Advanced clear cell renal cell carcinoma (ccRCC) frequently causes systemic inflammation. Recent studies have shown that cancer cells reshape the immune landscape by secreting cytokines or chemokines. This phenotype, called cancer-cell-intrinsic inflammation, triggers a metastatic cascade. Here, we identified the functional role and regulatory mechanism of inflammation driven by advanced ccRCC cells. The inflammatory nature of advanced ccRCC was recapitulated in a preclinical model of ccRCC. Amplification of cancer-cell-intrinsic inflammation during ccRCC progression triggered neutrophil-dependent lung metastasis. Massive expression of inflammation-related genes was transcriptionally activated by epigenetic remodelling through mechanisms such as DNA demethylation and super-enhancer formation. A bromodomain and extra-terminal motif inhibitor synchronously suppressed C-X-C-type chemokines in ccRCC cells and decreased neutrophil-dependent lung metastasis. Overall, our findings provide insight into the nature of inflammatory ccRCC, which triggers metastatic cascades, and suggest a potential therapeutic strategy.
高级透明细胞肾细胞癌 (ccRCC) 常引起全身炎症。最近的研究表明,癌细胞通过分泌细胞因子或趋化因子重塑免疫景观。这种表型称为癌细胞固有炎症,引发转移级联反应。在这里,我们确定了由高级 ccRCC 细胞驱动的炎症的功能作用和调控机制。ccRCC 的炎症性质在 ccRCC 的临床前模型中得到了重现。ccRCC 进展过程中癌细胞固有炎症的扩增触发了中性粒细胞依赖性肺转移。通过诸如 DNA 去甲基化和超级增强子形成等机制的表观遗传重塑,大量炎症相关基因的转录被激活。溴结构域和末端外基序抑制剂同步抑制 ccRCC 细胞中的 C-X-C 型趋化因子,并减少中性粒细胞依赖性肺转移。总的来说,我们的研究结果深入了解了引发转移级联反应的炎症性 ccRCC 的本质,并提出了一种潜在的治疗策略。