Wu Liqiang, Zhang Xiuxia, Lin Xiaojie, Wang Bo, Huang Chang, Qin Yao, Lin Shengyun
Department of Hematology, First Hospital Affiliated to Zhejiang University of Traditional Chinese Medicine, Hangzhou, Zhejiang 310006, P.R. China.
Department of General Surgery, Yuhang First People's Hospital, Hangzhou, Zhejiang 311100, P.R. China.
Exp Ther Med. 2018 Feb;15(2):2020-2026. doi: 10.3892/etm.2017.5627. Epub 2017 Dec 14.
Flavonoids, a vast group of polyphenols widely distributed in plants, are known to possess a range of biological activities and potential anti-tumor effects. X-linked inhibitor of apoptosis protein (XIAP) promotes the progression of leukemia by preventing tumor cells undergoing apoptosis. The present study investigated the potential effects and underlying mechanisms of pure total flavonoids from Macfad (PTFC) on human U937 cells, and explored the effects of short hairpin (sh)RNA-mediated XIAP knockdown on the anti-cancer effects of PTFC. Western blotting was used to determine level of apoptosis-associated effectors following PTFC treatment. A lentiviral vector of RNA interference of XIAP gene was constructed to downregulate XIAP expression. MTT assay and flow cytometry were used to determine the effects of PTFC separately or combined with XIAP-shRNA on inhibition and apoptosis of U937 cells, respectively. Treatment with PTFC effectively inhibited leukemic cell proliferation in a dose- and time-dependent manner. PTFC induced apoptosis of U937 cells in a dose-dependent manner, at a particular concentration range, by decreasing XIAP expression levels and activating caspases-3, -7 and -9. PTFC treatment combined with XIAP-shRNA additionally demonstrated a marked increase in cell apoptosis, compared with PTFC or XIAP-shRNA alone (P<0.05). Therefore, these findings suggest that PTFC inhibits growth and induces apoptosis in U937 cells . Furthermore, suppression of XIAP expression enhances these effects.
黄酮类化合物是广泛分布于植物中的一大类多酚,已知具有一系列生物活性和潜在的抗肿瘤作用。X连锁凋亡抑制蛋白(XIAP)通过阻止肿瘤细胞凋亡促进白血病进展。本研究探讨了光叶菝葜纯总黄酮(PTFC)对人U937细胞的潜在作用及其潜在机制,并探讨了短发夹(sh)RNA介导的XIAP基因敲低对PTFC抗癌作用的影响。采用蛋白质免疫印迹法检测PTFC处理后凋亡相关效应蛋白的水平。构建XIAP基因RNA干扰慢病毒载体下调XIAP表达。分别采用MTT法和流式细胞术检测PTFC单独或联合XIAP-shRNA对U937细胞抑制和凋亡的影响。PTFC处理能以剂量和时间依赖性方式有效抑制白血病细胞增殖。在特定浓度范围内,PTFC通过降低XIAP表达水平并激活半胱天冬酶-3、-7和-9,以剂量依赖性方式诱导U937细胞凋亡。与单独使用PTFC或XIAP-shRNA相比,PTFC与XIAP-shRNA联合处理可显著增加细胞凋亡(P<0.05)。因此,这些发现表明PTFC可抑制U937细胞生长并诱导其凋亡。此外,抑制XIAP表达可增强这些作用。