Jiali Zhao, Guifang Zeng, En Lin, Chaonong Cai, Peiping Li, Baojia Zou, Jian Li
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引用次数: 3
Abstract
Background: Hypoxia-inducible factor-1α (HIF-1α) or sonic hedgehog (SHH) is associated with hepatocellular carcinoma (HCC) progression. Hypoxia inhibits ferroptosis, which induces cancer cell death. However, the correlation between the combined HIF-1α and SHH up-regulation with prognosis, and the association between SHH and ferroptosis remain unclear. This study aimed to investigate them.
Methods: We detected the expression of HIF-1α and SHH in HCC. Cox regression, clinical data, and Kaplan-Meier analyses were performed. In vitro cell experiments verified the relationship between HIF-1α and SHH, and observed the invasion of hypoxic HCC cells. The correlation between SHH and ferroptosis was also analyzed.
Results: HIF-1α and SHH expression levels were significantly correlated with HCC (p < 0.0001). HIF-1α and SHH expression levels were found to be associated with TNM stage (p = 0.0121, p = 0.0078, respectively), vascular invasion (p < 0.0001, p < 0.0001, respectively), and recurrence (p = 0.0212, p = 0.0392, respectively). The combined upregulation of HIF-1α and SHH was an independent factor for predicting the overall survival (OS) of patients with HCC (p = 0.003), who had the shortest OS (p = 0.0009). SHH paralleled the increase in HIF-1α expression, which promotes cancer cell invasion. The upregulation of SHH was related to the inhibition of the expression of ferroptosis-related factors (FANCD2, p < 0.0001 and FTH1, p = 0.0009) in HCC.
Conclusion: Combined HIF-1α and SHH upregulation is a potentially poor prognosis indicator in patients with HCC because the upregulation of SHH inhibits ferroptosis in hypoxic cancer cells.
背景:缺氧诱导因子-1α (HIF-1α)或音hedgehog基因(SHH)与肝细胞癌(HCC)的进展有关。缺氧抑制铁下垂,导致癌细胞死亡。然而,HIF-1α和SHH联合上调与预后的关系,以及SHH与铁下垂的关系尚不清楚。这项研究旨在调查他们。方法:检测肝癌组织中HIF-1α和SHH的表达。进行Cox回归、临床资料和Kaplan-Meier分析。体外细胞实验证实了HIF-1α与SHH之间的关系,并观察到缺氧HCC细胞的侵袭。我们还分析了SHH与铁下垂的相关性。结果:HIF-1α和SHH表达水平与肝癌(p = 0.0121, p = 0.0078)、血管侵犯(p = 0.0212, p = 0.0392)有显著相关性。HIF-1α和SHH的联合上调是预测HCC患者总生存期(OS)的独立因素(p = 0.003),其OS最短(p = 0.0009)。SHH平行于HIF-1α表达的增加,从而促进癌细胞的侵袭。SHH的上调与抑制肝癌中铁凋亡相关因子(FANCD2, p p = 0.0009)的表达有关。结论:HIF-1α和SHH联合上调是HCC患者潜在的不良预后指标,因为SHH上调可抑制缺氧癌细胞的铁下垂。