Jiangsu Key Laboratory of TCM Evaluation and Translational Research, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 639 Longmian Road, Nanjing 211198, China.
Int J Biol Sci. 2020 Jan 1;16(3):396-407. doi: 10.7150/ijbs.34978. eCollection 2020.
As the most frequent cause of cancer-related death worldwide, lung cancer is closely related to inflammation. The interaction between tumor cells and inflammatory cells promotes tumor development and metastasis. During tumor development, vascular endothelial cells form the most important barrier to prevent tumor cell migration to the blood and tissue. Increased vascular permeability provides favorable conditions for the migration of tumor cells, and endothelial tight junctions are an important component of the vascular barrier. Protein kinase C δ is involved in the occurrence of non-small cell lung cancer and regulates vascular permeability and tight junction protein expression. Src kinase was reported to play an important role in TNF-α-induced endothelial inflammation. Ophiopogon Saponin C1 is a new chemical compound isolated from , but its pharmacological activities have not been fully elucidated. Therefore, we tested the protective effects of C1 on endothelial permeability in a model of TNF-α-induced endothelial inflammation by transendothelial electrical resistance and sodium fluorescein assays and verified these results in a nude mouse model of experimental pulmonary adenocarcinoma metastasis. We further elucidated the mechanism of C1, which was based on the PKCδ and Src proteins, by Western blotting. C1 can inhibit lung cancer in vivo, regulate the level of plasma inflammation in tumor-bearing mice, and protect the pulmonary vascular barrier against injury induced by cancer. It was investigated the expression and distribution of the TJ index protein ZO-1 in mouse vascular endothelium and HUVECs and found that C1 could inhibit the degradation and breakage of the ZO-1 protein. Related signaling experiments confirmed that C1 can inhibit TNF-α and activation of PKCδ and Src kinase. This study laid the foundation for further analysis of new drugs with clear mechanisms and independent intellectual property rights of traditional Chinese medicines.
作为全球最常见的癌症相关死因,肺癌与炎症密切相关。肿瘤细胞与炎症细胞的相互作用促进了肿瘤的发展和转移。在肿瘤发展过程中,血管内皮细胞形成了阻止肿瘤细胞迁移到血液和组织的最重要屏障。血管通透性的增加为肿瘤细胞的迁移提供了有利条件,而内皮紧密连接是血管屏障的重要组成部分。蛋白激酶 Cδ(PKCδ)参与非小细胞肺癌的发生,并调节血管通透性和紧密连接蛋白的表达。Src 激酶被报道在 TNF-α诱导的内皮炎症中发挥重要作用。麦冬皂苷 C1 是从麦冬中分离得到的一种新的化学化合物,但它的药理活性尚未完全阐明。因此,我们通过跨内皮电阻和荧光素钠检测实验,在 TNF-α诱导的内皮炎症模型中测试了 C1 对内皮通透性的保护作用,并在实验性肺腺癌转移的裸鼠模型中验证了这些结果。我们通过 Western blot 进一步阐明了 C1 的作用机制,该机制基于 PKCδ 和 Src 蛋白。C1 可以抑制体内肺癌的发生,调节荷瘤小鼠血浆炎症水平,保护肺血管屏障免受癌症引起的损伤。我们研究了 C1 对小鼠血管内皮和 HUVECs 中 TJ 指数蛋白 ZO-1 的表达和分布的影响,发现 C1 可以抑制 ZO-1 蛋白的降解和断裂。相关信号转导实验证实,C1 可以抑制 TNF-α和 PKCδ及 Src 激酶的激活。这项研究为进一步分析具有明确作用机制和中药自主知识产权的新药奠定了基础。