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干扰素-λ 3 与索拉非尼协同作用抑制肝癌增殖。

Synergy with interferon-lambda 3 and sorafenib suppresses hepatocellular carcinoma proliferation.

机构信息

Department of General Surgery, Lanzhou University Second Hospital, Lanzhou 730030, PR China; Hepato-Biliary-Pancreatic Institute, Lanzhou University Second Hospital, Lanzhou 730030, PR China; Gansu Provincial-Level Key Laboratory of Digestive System Tumors, Lanzhou 730030, PR China.

Hepato-Biliary-Pancreatic Institute, Lanzhou University Second Hospital, Lanzhou 730030, PR China; Gansu Provincial-Level Key Laboratory of Digestive System Tumors, Lanzhou 730030, PR China; Division of Liver Disease, Lanzhou University Second Hospital, Lanzhou 730030, PR China.

出版信息

Biomed Pharmacother. 2017 Apr;88:395-402. doi: 10.1016/j.biopha.2017.01.077. Epub 2017 Jan 22.

Abstract

Hepatocellular carcinoma (HCC) is a common and fatal malignancy of the liver. Sorafenib is a small molecule multikinase inhibitor that acts against different cancer cell lines and is used for the treatment of HCC. However, some advanced HCC patients fail to respond to sorafenib, and those who do lack a meaningful clinical benefit. Interferon-lambda 3 (IFN-λ3) is a type III interferon with antiviral, antiproliferative, and immunomodulatory functions. Here, we evaluated the use of IFN-λ3 as an adjuvant treatment with sorafenib in HCC. In the present study, CCK-8 and colony formation assay results showed that treatment with a combination of IFN-λ3 and sorafenib suppresses the viability of HepG2 and SMMC7721 liver cancer cell lines more than treatment with either alone. In addition, flow cytometry results confirmed that treatment with a combination of IFN-λ3 and sorafenib promotes the loss of mitochondrial membrane potential and induces the production of ROS more than treatment with either alone. Furthermore, using a subcutaneous SMMC7721 tumor model, treatment with a combination of IFN-λ3 and sorafenib significantly reduced the tumor growth/volume and induced apoptosis compared to treatment with sorafenib alone. These results show that combined treatment with IFN-λ3 and sorafenib facilitates a synergistic effect on suppressing HCC cancer growth and promoting cell apoptosis in vitro and in vivo. Thus, IFN-λ3 in combination with sorafenib might prove to be a useful adjunctive strategy for the clinical treatment of HCC.

摘要

肝细胞癌(HCC)是肝脏常见且致命的恶性肿瘤。索拉非尼是一种小分子多激酶抑制剂,可作用于不同的癌细胞系,用于治疗 HCC。然而,一些晚期 HCC 患者对索拉非尼没有反应,而那些有反应的患者缺乏有意义的临床获益。干扰素-λ3(IFN-λ3)是一种具有抗病毒、抗增殖和免疫调节功能的 III 型干扰素。在这里,我们评估了 IFN-λ3 作为索拉非尼辅助治疗 HCC 的用途。在本研究中,CCK-8 和集落形成实验结果表明,IFN-λ3 和索拉非尼联合治疗比单独使用任一药物更能抑制 HepG2 和 SMMC7721 肝癌细胞系的活力。此外,流式细胞术结果证实,IFN-λ3 和索拉非尼联合治疗比单独使用任一药物更能促进线粒体膜电位丧失和诱导 ROS 产生。此外,使用皮下 SMMC7721 肿瘤模型,IFN-λ3 和索拉非尼联合治疗与单独使用索拉非尼相比,显著降低了肿瘤生长/体积并诱导了细胞凋亡。这些结果表明,IFN-λ3 与索拉非尼联合治疗可在体外和体内协同抑制 HCC 肿瘤生长和促进细胞凋亡。因此,IFN-λ3 联合索拉非尼可能被证明是 HCC 临床治疗的有用辅助策略。

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