Department of Oncology, First Hospital of Lanzhou University, Lanzhou, Gansu, China (mainland).
Provincial-Level Key Laboratory for Molecular Medicine of Major Diseases and The Prevention and Treatment with Traditional Chinese Medicine Research in Gansu Colleges and University, Lanzhou, Gansu, China (mainland).
Med Sci Monit. 2019 Jun 2;25:4110-4121. doi: 10.12659/MSM.914219.
BACKGROUND The tumor microenvironment in lung cancer plays an important role in tumor progression and metastasis. Bone marrow-derived mesenchymal stem cells (MSCs) co-cultured with A549 lung cancer cells show changes in morphology, increase cell proliferation, and cell migration. This study aimed to investigate the effects of Astragalus polysaccharide (APS), a traditional Chinese herbal medicine, on the changes induced in bone marrow-derived MSCs by A549 lung cancer cells in vitro. MATERIAL AND METHODS Bone marrow-derived MSCs were co-cultured with A549 cells (Co-BMSCs). Co-cultured bone marrow-derived MSCs and A549 cells treated with 50 μg/ml of APS (Co-BMSCs + APS) were compared with untreated Co-BMSCs. Cell proliferation was measured using the cell counting kit-8 (CCK-8) assay. Flow cytometry evaluated the cell cycle. Microarray assays for mRNA expression and Western blot for protein expression were used. RESULTS Compared with untreated Co-BMSCs, APS treatment of Co-BMSCs improved cell morphology, reduced cell proliferation, and inhibited cell cycle arrest. The mitogen-activated protein kinase (MAPK)/nuclear factor-kappa B (NF-kappaB) pathway, TP53, caspase-3, acetylated H4K5, acetylated H4K8, and acetylated H3K9 were involved in the regulatory process. CONCLUSIONS APS treatment reduced cell proliferation and morphological changes in bone marrow-derived MSCs that were co-cultured with A549 lung cancer cells in vitro.
肺癌肿瘤微环境在肿瘤的演进和转移中起着重要作用。与 A549 肺癌细胞共培养的骨髓间充质干细胞(MSCs)在形态上发生变化,细胞增殖增加,细胞迁移。本研究旨在探讨中药黄芪多糖(APS)对 A549 肺癌细胞体外诱导的骨髓间充质干细胞变化的影响。
骨髓间充质干细胞与 A549 细胞共培养(Co-BMSCs)。将未处理的 Co-BMSCs 与用 50μg/ml APS 处理的共培养骨髓间充质干细胞和 A549 细胞(Co-BMSCs+APS)进行比较。用细胞计数试剂盒-8(CCK-8)法检测细胞增殖。流式细胞术评估细胞周期。用微阵列分析 mRNA 表达,用 Western blot 分析蛋白表达。
与未处理的 Co-BMSCs 相比,APS 处理 Co-BMSCs 改善了细胞形态,降低了细胞增殖,并抑制了细胞周期停滞。丝裂原活化蛋白激酶(MAPK)/核因子-κB(NF-κB)通路、TP53、半胱氨酸天冬氨酸蛋白酶-3(caspase-3)、乙酰化 H4K5、乙酰化 H4K8 和乙酰化 H3K9 参与了调节过程。
APS 处理减少了体外与 A549 肺癌细胞共培养的骨髓间充质干细胞的增殖和形态变化。