Du Jia-Yi, Zhang Chu-Ting, Li Ting, Li Ya-Ping
Laboratory of Epidemiology and Public Health, Yale University School of Public Health, New Haven, CT 06510, United States.
Department of Infectious Diseases, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, Shaanxi Province, China.
World J Hepatol. 2024 Dec 27;16(12):1371-1376. doi: 10.4254/wjh.v16.i12.1371.
In this manuscript we comment on the article by Yang published recently, focusing on how hepatic angiopoietin-2 (Ang-2) transcription promote the progression of hepatocellular carcinoma (HCC). HCC is one of the most common and lethal malignancies worldwide, especially in regions with high hepatitis B virus infection rates. Ang-2 is a key mediator of angiogenesis and plays a significant role in the progression of chronic liver diseases towards HCC, particularly in the hypoxic microenvironment. This paper reviews the dynamic expression of Ang-2 in hepatocarcinogenesis and its regulation by hypoxia-inducible factor-1α. Furthermore, we discuss Ang-2's potential as an early monitoring biomarker for metastasis, and the therapeutic prospects of silencing hypoxia-inducible factor-1α to downregulate Ang-2 and suppress epithelial-mesenchymal transition in HCC treatment.
在本手稿中,我们对Yang最近发表的文章进行评论,重点关注肝血管生成素-2(Ang-2)转录如何促进肝细胞癌(HCC)的进展。HCC是全球最常见且致命的恶性肿瘤之一,尤其是在乙型肝炎病毒感染率高的地区。Ang-2是血管生成的关键介质,在慢性肝病向HCC的进展中起重要作用,特别是在缺氧微环境中。本文综述了Ang-2在肝癌发生中的动态表达及其受缺氧诱导因子-1α的调控。此外,我们讨论了Ang-2作为转移早期监测生物标志物的潜力,以及沉默缺氧诱导因子-1α以下调Ang-2并抑制HCC治疗中上皮-间质转化的治疗前景。