Vanderborght Bart, De Muynck Kevin, Lefere Sander, Geerts Anja, Degroote Helena, Verhelst Xavier, Van Vlierberghe Hans, Devisscher Lindsey
Department of Internal Medicine and Pediatrics, Department of Gastroenterology and Hepatology, Hepatology Research Unit, Ghent University, Ghent, Belgium.
Department of Basic and Applied Medical Sciences, Gut-Liver Immunopharmacology Unit, Ghent University, Ghent, Belgium.
Oncotarget. 2020 Dec 1;11(48):4504-4520. doi: 10.18632/oncotarget.27830.
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death worldwide. For advanced HCC, there is still an unmet need for more effective therapeutic strategies. HCC is typically associated with hypoxia and the hypoxia-inducible factor (HIF) regulatory pathway plays an important role in HCC development and progression. Therefore, we investigated the therapeutic potential of isoform-specific HIF-1α and HIF-2α antisense oligonucleotides (ASOs), along with their effect on the inflammatory and fibrotic component of the tumor microenvironment (TME), in an experimental HCC mouse model. Based on its efficacy and safety, a dosage regimen of 20 mg/kg intraperitoneal injection of HIFα ASO twice per week was selected for further investigation in a preventive and therapeutic setting in a N,N-diethylnitrous amide (DEN)-induced HCC mouse model. DEN administration resulted in 100% tumor formation and HIFα ASO administration led to effective and selective hepatic downregulation of its target genes. HIFα ASO treatment had no effect on tumor numbers, but even enhanced the increased hepatic expression of HCC tumor markers, α-fetoprotein and glypican-3, compared to scrambled control ASO treatment in HCC mice. Especially HIF-1α ASO treatment resulted in an enhanced increase of monocytes and monocyte-derived macrophages in the liver and an enhanced hepatic upregulation of inflammatory markers. Both HIFα ASOs aggravated liver fibrosis in HCC mice compared to scrambled ASO treatment. The observed effects of our dosing regimen for HIF-1α and HIF-2α ASO treatment in the DEN-induced HCC mouse model discourage the use of HIFα isoforms as targets for the treatment of HCC.
肝细胞癌(HCC)是全球癌症相关死亡的主要原因之一。对于晚期HCC,仍然迫切需要更有效的治疗策略。HCC通常与缺氧相关,缺氧诱导因子(HIF)调节通路在HCC的发生和发展中起重要作用。因此,我们在实验性HCC小鼠模型中研究了亚型特异性HIF-1α和HIF-2α反义寡核苷酸(ASO)的治疗潜力,以及它们对肿瘤微环境(TME)炎症和纤维化成分的影响。基于其疗效和安全性,选择每周两次腹腔注射20 mg/kg HIFα ASO的给药方案,在N,N-二乙基亚硝胺(DEN)诱导的HCC小鼠模型中进行预防和治疗研究。给予DEN导致100%的肿瘤形成,给予HIFα ASO导致其靶基因在肝脏中有效且选择性地下调。与HCC小鼠中乱序对照ASO治疗相比,HIFα ASO治疗对肿瘤数量没有影响,但甚至增强了HCC肿瘤标志物甲胎蛋白和磷脂酰肌醇蛋白聚糖-3在肝脏中的表达增加。特别是HIF-1α ASO治疗导致肝脏中单核细胞和单核细胞衍生巨噬细胞的增加增强,以及炎症标志物在肝脏中的上调增强。与乱序ASO治疗相比,两种HIFα ASO均加重了HCC小鼠的肝纤维化。我们在DEN诱导的HCC小鼠模型中对HIF-1α和HIF-2α ASO治疗的给药方案所观察到的效果不支持将HIFα亚型用作HCC治疗的靶点。