Li Xian, Li Shanshan, Pang Jinlong, Huang Fuhao, Guo Bin, Liu Hao
School of Pharmacy, Bengbu Medical College, Bengbu 2330302, China.
Anhui Provincial Key Laboratory of New Technology of Chinese Herbal Pieces Manufacturing, Bozhou 236800, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2020 Sep 30;40(9):1332-1339. doi: 10.12122/j.issn.1673-4254.2020.09.17.
To assess the changes in the effects of cantharides after alkaline processing on proliferation, migration, invasion, and apoptosis of human lung cancer A549 cells.
Human non-small cell lung cancer A549 cells were treated with cantharis extract (CTE) from raw cantharides and alkali processed cantharis extract (ACE). The proliferation of the cells was detected with CCK-8 assay, and the cell migration and invasion were assessed using wound healing assay and Transwell assay, respectively. The expressions of MMP1 and MMP2 in the cells were detected using Western blotting, the contents of IFN-γ, IL-1β and TNF-α were measured with ELISA, and cell apoptosis was analyzed with annexinV/PI fluorescent staining.
Both CTE and ACE significantly reduced the viability and inhibited the migration of A549 cells, and high-dose ACE produced a significantly stronger inhibitory effect on cell migration than high- dose CTE ( < 0.01). ACE showed more potent inhibitory effect than CTE on the invasion of A549 cells ( < 0.01). Both CTE and ACE inhibited the expressions of MMP1 and MMP2 and up-regulated the level of IFN-γ without significantly affecting the levels of IL-1β and TNF-α. Annexin V/PI staining showed that both CTE and ACE caused apoptosis of A549 cells, but ACE had a stronger proapoptotic effect.
Processing with sodium hydroxide can significantly improve the antitumor activity of cantharides, which inhibits the proliferation, migration and invasion of A549 cells possibly by down-regulating the expressions of MMP1 and MMP2, promoting apoptosis and increasing the level of IFN-γ.
评估斑蝥经碱性处理后对人肺癌A549细胞增殖、迁移、侵袭及凋亡作用的变化。
用人非小细胞肺癌A549细胞分别给予生斑蝥提取物(CTE)和碱处理斑蝥提取物(ACE)。采用CCK-8法检测细胞增殖,分别用划痕实验和Transwell实验评估细胞迁移和侵袭。用蛋白质免疫印迹法检测细胞中MMP1和MMP2的表达,用酶联免疫吸附测定法检测IFN-γ、IL-1β和TNF-α的含量,用膜联蛋白V/碘化丙啶荧光染色分析细胞凋亡。
CTE和ACE均显著降低A549细胞活力并抑制其迁移,高剂量ACE对细胞迁移的抑制作用显著强于高剂量CTE(<0.01)。ACE对A549细胞侵袭的抑制作用比CTE更强(<0.01)。CTE和ACE均抑制MMP1和MMP2的表达并上调IFN-γ水平,而对IL-1β和TNF-α水平无显著影响。膜联蛋白V/碘化丙啶染色显示CTE和ACE均导致A549细胞凋亡,但ACE的促凋亡作用更强。
用氢氧化钠处理可显著提高斑蝥的抗肿瘤活性,其可能通过下调MMP1和MMP2的表达、促进凋亡及提高IFN-γ水平来抑制A549细胞的增殖、迁移和侵袭。