Department of Biomedical Sciences, University of Padova, Viale G. Colombo 3, 35121 Padova, Italy.
Genes (Basel). 2024 Sep 5;15(9):1167. doi: 10.3390/genes15091167.
The oxygen-sensing pathway is a crucial regulatory circuit that defines cellular conditions and is extensively exploited in cancer development. Pathogenic mutations in the von Hippel-Lindau (VHL) tumour suppressor impair its role as a master regulator of hypoxia-inducible factors (HIFs), leading to constitutive HIF activation and uncontrolled angiogenesis, increasing the risk of developing clear cell renal cell carcinoma (ccRCC). HIF hyperactivation can sequester HIF-1β, preventing the aryl hydrocarbon receptor (AHR) from correctly activating gene expression in response to endogenous and exogenous ligands such as TCDD (dioxins). In this study, we used protein-protein interaction networks and gene expression profiling to characterize the impact of VHL loss on AHR activity. Our findings reveal specific expression patterns of AHR interactors following exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and in ccRCC. We identified several AHR interactors significantly associated with poor survival rates in ccRCC patients. Notably, the upregulation of the androgen receptor (AR) and retinoblastoma-associated protein (RB1) by TCDD, coupled with their respective downregulation in ccRCC and association with poor survival rates, suggests novel therapeutic targets. The strategic activation of the AHR via selective AHR modulators (SAhRMs) could stimulate its anticancer activity, specifically targeting RB1 and AR to reduce cell cycle progression and metastasis formation in ccRCC. Our study provides comprehensive insights into the complex interplay between the AHR and HIF pathways in ccRCC pathogenesis, offering novel strategies for targeted therapeutic interventions.
氧感应通路是一个关键的调节回路,它定义了细胞状态,并在癌症发展中得到广泛利用。von Hippel-Lindau(VHL)肿瘤抑制因子的致病突变会损害其作为缺氧诱导因子(HIFs)的主调控因子的作用,导致 HIF 的组成性激活和不受控制的血管生成,增加发展为透明细胞肾细胞癌(ccRCC)的风险。HIF 的过度激活可以隔离 HIF-1β,阻止芳香烃受体(AHR)在响应内源性和外源性配体(如 TCDD(二恶英))时正确激活基因表达。在这项研究中,我们使用蛋白质-蛋白质相互作用网络和基因表达谱来描述 VHL 缺失对 AHR 活性的影响。我们的研究结果揭示了 VHL 缺失后 AHR 活性的特定表达模式,以及在 ccRCC 中的表达模式。我们确定了几个与 ccRCC 患者生存率显著相关的 AHR 相互作用蛋白。值得注意的是,TCDD 上调雄激素受体(AR)和视网膜母细胞瘤相关蛋白(RB1),同时在 ccRCC 中下调,并与生存率降低相关,提示了新的治疗靶点。通过选择性 AHR 调节剂(SAhRMs)策略性地激活 AHR,可以刺激其抗癌活性,特别是针对 RB1 和 AR,以减少 ccRCC 中的细胞周期进展和转移形成。我们的研究提供了对 AHR 和 HIF 通路在 ccRCC 发病机制中复杂相互作用的全面了解,为靶向治疗干预提供了新的策略。