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TNF-α is a potential therapeutic target to overcome sorafenib resistance in hepatocellular carcinoma

机译:TNF-α是克服肝细胞癌中索拉非尼抗性的潜在治疗靶标

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摘要

Background: The role of tumor necrosis factor alpha (TNF-α) in targeted therapy for hepatocellular carcinoma (HCC) remains largely unknown. The current study aimed to clarify the mechanistic effects of targeting TNF-α to overcome sorafenib resistance in HCC. Methods: A correlation of TNF-α expression with the prognosis was analyzed in 62 HCC patients who underwent surgical resection and subsequent received adjuvant sorafenib treatment. The relation of TNF-α expression and sorafenib sensitivity was determined in different HCC cell lines. The combined therapeutic effects of sorafenib and ulinastatin, which could inhibit TNF-α expression, on HCC were examined in vitro and in vivo. Findings: High TNF-α expression was correlated with poor outcomes in HCC patients who received adjuvant sorafenib after surgery. In vitro experiments showed that TNF-α promotes HCC cell resistant to sorafenib through inducing epithelial-mesenchymal transition (EMT). Notably, the current study revealed that sorafenib has no significant influence on the expression and secretion of TNF-α, and sorafenib had limited effectiveness on reversing EMT in HCC cells with high TNF-α expression. Inhibiting the expression of TNF-α with ulinastatin significantly enhanced the anti-tumor effect of sorafenib on HCC cells with high expression of TNF-α in vitro and in vivo.Interpretation: Our findings indicate that TNF-α may serve as a novel predictor of sorafenib sensitivity in HCC patients. Sorafenib combined with ulinastatin may improve the effectiveness of treatment of HCC in patients with high expression of TNF-α. Fund: This work was supported by grants from the National Natural Science Foundation of China (no.81572398; no.81672419), the Science and Technology Planning Project of Guangdong Province (no. 2017A010105003; no.2015A050502023; no.2016A020216010), and the Natural Science Foundation of Guangdong Province (no.2014A030313061; no. 2013B021800101). Keywords: Hepatocellular carcinoma, Sorafenib resistance, TNF-α, Ulinastatin, Combination treatment
机译:背景:肿瘤坏死因子α(TNF-α)在针对肝细胞癌(HCC)的靶向治疗中的作用仍然很大程度上。目前的研究旨在阐明靶向TNF-α的机械效应来克服HCC中的索拉非尼抗性。方法:在62次HCC患者中分析了TNF-α表达与预后的表达在手术切除和随后接受佐剂Sorafenib治疗中进行了预后的相关性。在不同的HCC细胞系中测定TNF-α表达和索拉非尼敏感性的关系。在体外和体内,研究了索拉非尼和乌纳替肽的组合治疗效果,可以抑制HCC的TNF-α表达。结果:高TNF-α表达与HCC患者在手术后接受佐剂Sorafenib的患者的差异相关。体外实验表明,TNF-α通过诱导上皮 - 间充质转换(EMT)来促进耐索拉非尼的HCC电池。值得注意的是,目前的研究表明,索拉非尼对TNF-α的表达和分泌没有显着影响,并且索拉非尼对具有高TNF-α表达的HCC细胞中的EMT有限的有效性。抑制TNF-α的表达与乌氏菌素显着提高了Sorafenib对HCC细胞的抗肿瘤作用,在体外和体内含有高表达TNF-α。interpropation:我们的研究结果表明TNF-α可以作为一种新的预测因子索拉非尼患者HCC患者的敏感性。索拉非尼与乌凡汀联合ulinastatin可以改善TNF-α高表达患者治疗HCC的有效性。基金:中国自然科学基金的补助金(No.81572398; 81672419号),广东省科技规划项目得到了支持(No.2110505023; No.2016A020216010),以及广东省自然科学基金(No.2014A030313061; NO。2013B021800101)。关键词:肝细胞癌,索拉染料,TNF-α,乌纳替肽,组合治疗

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