Kurma Keerthi, Manches Olivier, Chuffart Florent, Sturm Nathalie, Gharzeddine Khaldoun, Zhang Jianhui, Mercey-Ressejac Marion, Rousseaux Sophie, Millet Arnaud, Lerat Herve, Marche Patrice N, Macek Jilkova Zuzana, Decaens Thomas
Université Grenoble Alpes, 38000 Grenoble, France.
Institute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.
Cancers (Basel). 2021 Oct 4;13(19):4981. doi: 10.3390/cancers13194981.
Hepatocellular carcinoma (HCC) is the most common type of liver cancer. The majority of HCC cases are associated with liver fibrosis or cirrhosis developing from chronic liver injuries. The immune system of the liver contributes to the severity of tissue damage, the establishment of fibrosis and the disease's progression towards HCC. Herein, we provide a detailed characterization of the DEN-induced HCC rat model during fibrosis progression and HCC development with a special focus on the liver's inflammatory microenvironment. Fischer 344 male rats were treated weekly for 14 weeks with intra-peritoneal injections of 50 mg/kg DEN. The rats were sacrificed before starting DEN-injections at 0 weeks, after 8 weeks, 14 weeks and 20 weeks after the start of DEN-injections. We performed histopathological, immunohistochemical, RT-qPCR, RNA-seq and flow cytometry analysis. Data were compared between tumor and non-tumor samples from the DEN-treated versus untreated rats, as well as versus human HCCs. Chronic DEN injections lead to liver damage, hepatocytes proliferation, liver fibrosis and cirrhosis, disorganized vasculature, and a modulated immune microenvironment that mimics the usual events observed during human HCC development. The RNA-seq results showed that DEN-induced liver tumors in the rat model shared remarkable molecular characteristics with human HCC, especially with HCC associated with high proliferation. In conclusion, our study provides detailed insight into hepatocarcinogenesis in a commonly used model of HCC, facilitating the future use of this model for preclinical testing.
肝细胞癌(HCC)是最常见的肝癌类型。大多数HCC病例与慢性肝损伤导致的肝纤维化或肝硬化有关。肝脏的免疫系统会影响组织损伤的严重程度、纤维化的形成以及疾病向HCC的进展。在此,我们详细描述了二乙基亚硝胺(DEN)诱导的HCC大鼠模型在纤维化进展和HCC发生过程中的情况,特别关注肝脏的炎性微环境。Fischer 344雄性大鼠每周腹腔注射50 mg/kg DEN,共注射14周。在0周(开始注射DEN前)、注射DEN后8周、14周和20周时处死大鼠。我们进行了组织病理学、免疫组织化学、逆转录定量聚合酶链反应(RT-qPCR)、RNA测序(RNA-seq)和流式细胞术分析。将DEN处理组与未处理组大鼠的肿瘤和非肿瘤样本的数据进行比较,同时也与人类HCC的数据进行比较。长期注射DEN会导致肝损伤、肝细胞增殖、肝纤维化和肝硬化、血管紊乱以及免疫微环境的改变,这与人类HCC发生过程中常见的情况相似。RNA-seq结果表明,大鼠模型中DEN诱导的肝肿瘤与人类HCC具有显著的分子特征,尤其是与高增殖相关的HCC。总之,我们的研究为常用的HCC模型中的肝癌发生提供了详细的见解,有助于该模型在未来临床前测试中的应用。