巨噬细胞移动抑制因子
波形蛋白
癌症研究
A549电池
腺癌
上皮-间质转换
医学
癌症
癌细胞
细胞因子
免疫系统
安普克
炎症
肺癌
免疫学
病理
蛋白激酶A
转移
生物
免疫组织化学
激酶
内科学
细胞生物学
作者
Chien-Huang Liao,Chen-Yin Yong,Gi‐Ming Lai,Jyh-Ming Chow,Chieh-Fang Cheng,Chia-Lang Fang,Pei-Chun Lin,Chia-Lun Chang,Yu-Mei Zheng,Shuang‐En Chuang,Jacqueline Whang‐Peng,Chih‐Jung Yao
标识
DOI:10.1142/s0192415x20500731
摘要
Astragalus membranaceus is the most popular traditional Chinese medicine for managing vital energy deficiency. Its injectable polysaccharide PG2 has been used for relieving cancer-related fatigue, and PG2 has immune-modulatory and anti-inflammatory effects. In this study, we explored the effects of PG2 in lung adenocarcinoma A549 and CL1-2 cells and investigated its anticancer activity, and the results were validated in severe combined immunodeficiency (SCID) mice. Although PG2 did not inhibit the growth of these cells, it dose-dependently suppressed their migration and invasion, accompanied by reduced vimentin and AXL and induced epithelial cadherin (E-cadherin) expression. Regarding the underlying molecular mechanism, PG2 treatment reduced the macrophage migration inhibitory factor (MIF), an inflammatory cytokine that promotes the epithelial–mesenchymal transition and aggressiveness of cancer cells. Consistent with the previous finding that MIF regulates matrix metalloproteinase-13 (MMP-13) and AMP-activated protein kinase (AMPK), treatment with PG2 reduced MMP-13 and activated AMPK in A549 and CL1-2 cells in this study. In SCID mice injected with A549 cells through the tail vein, intraperitoneal injection with PG2 reduced lung and abdominal metastases in parallel with decreased immunohistochemical staining of AXL, vimentin, MMP-13, and MIF in the tumor. Collectively, data revealed a potential application of PG2 in integrative cancer treatment through the suppression of MIF in cancer cells and their aggressiveness.
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