The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of TCM), Hangzhou, 310006, China.
Department of Oncology, Xijing Hospital, Air Force Military Medical University, 15 Changle West Road, Xian, 710032, Shaanxi, China.
Mol Genet Genomics. 2021 May;296(3):571-579. doi: 10.1007/s00438-020-01759-6. Epub 2021 Feb 12.
This study aimed to investigate the effects of the total flavonoids of Radix Tetrastigma (RTF) on inflammation-related hepatocellular carcinoma (HCC) development. Extracted RTF was diluted to different concentrations for subsequent experiments. HCC cells were cotreated with lipopolysaccharide (LPS) and RTF to investigate the effects of RTF on LPS-stimulated HCC cells. A CCK-8 kit was used to measure cell proliferation. Apoptosis was detected with a flow cytometer. Cell migration and invasion were quantified by wound healing and Transwell assays, respectively. The expression of TLR4 and COX-2 and activation of the NF-κB pathway were determined by Western blotting. Treatment with LPS significantly enhanced cell proliferation and decreased the apoptosis rate, while cell migration and invasion were notably upregulated. RTF suppressed the proliferation and invasion induced by LPS stimulation and promoted HCC cell apoptosis. The protein levels of Bax and cleaved caspase-3 were decreased and that of Bcl-2 was increased by LPS in HCC cells, which could be rescued by RTF. RTF significantly inhibited the LPS-induced expression of the proinflammatory mediators IL-6 and IL-8 in HCC cells. Mechanistically, with RTF treatment, the upregulated expression of TLR4 and COX-2 induced by LPS was obviously downregulated. Furthermore, the phosphorylation of NF-κB/p65 was significantly decreased in LPS-stimulated cells after supplementation with RTF. Our study suggests that RTF exerts a significant inhibitory effect on the LPS-induced enhancement of the malignant behaviors of HCC cells via inactivation of TLR4/NF-κB signaling. RTF may be a promising chemotherapeutic agent to limit HCC development and inflammation-mediated metastasis.
本研究旨在探讨藤茶总黄酮(RTF)对炎症相关肝细胞癌(HCC)发展的影响。提取的 RTF 被稀释至不同浓度,用于后续实验。将 HCC 细胞与脂多糖(LPS)共同孵育,以研究 RTF 对 LPS 刺激的 HCC 细胞的影响。CCK-8 试剂盒用于测量细胞增殖。流式细胞术检测细胞凋亡。划痕愈合和 Transwell 实验分别用于定量细胞迁移和侵袭。Western blot 用于检测 TLR4 和 COX-2 的表达以及 NF-κB 通路的激活。LPS 处理显著增强了细胞增殖,降低了细胞凋亡率,同时显著上调了细胞迁移和侵袭。RTF 抑制了 LPS 刺激诱导的增殖和侵袭,并促进了 HCC 细胞凋亡。LPS 降低了 HCC 细胞中 Bax 和 cleaved caspase-3 的蛋白水平,增加了 Bcl-2 的蛋白水平,而 RTF 则挽救了这一现象。RTF 显著抑制了 LPS 诱导的 HCC 细胞中促炎介质 IL-6 和 IL-8 的表达。在机制上,用 RTF 处理后,LPS 诱导的 TLR4 和 COX-2 的表达上调明显下调。此外,补充 RTF 后,LPS 刺激的细胞中 NF-κB/p65 的磷酸化明显降低。我们的研究表明,RTF 通过抑制 TLR4/NF-κB 信号通路的激活,对 LPS 诱导的 HCC 细胞恶性行为增强具有显著的抑制作用。RTF 可能是一种有前途的化疗药物,可限制 HCC 的发展和炎症介导的转移。