Duan Pei-Feng, Jia Xiu-Hong, Wang Jian-Yong
Department of Pediatrics, Affiliated Hospital of Binzhou Medical University, Binzhou, Shandong 256603, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2015 Sep;17(9):989-93.
To study the effect of safflower injection on the proliferation and apoptosis of human leukemia cell line HEL and the relevant molecular mechanisms.
HEL cells were treated with different concentrations of safflower injection. HEL cells without safflower injection treatment were used as the control group. MTT method was used to detect the inhibitory rate of the HEL cells at 24, 48 and 72 hours after various concentrations of safflower injection treatment (10, 20, 30, 40 and 50 mg/mL). The cell cycle and apoptosis were detected using flow cytometry and the HOXB3-mRNA expression was measured by RT-PCR at 48 hours after safflower injection treatment (10, 20 and 30 mg/mL).
Compared with the control group, various concentrations of safflower injection inhibited HEL cell proliferation in a dose-dependent manner (P<0.05). At 48 hours after various concentrations of safflower injection treatment, the number of treated cells in the G2/M phase increased, but that in the S phase decreased, and the apoptosis rate was significantly higher than that in the control group, with a dose-dependent manner (P<0.05). The expression of HOXB3-mRNA in safflower injection-treated cells decreased in a dose-dependent manner compared with the control group (P<0.05).
Safflower injection can inhibit proliferation and induce apoptosis of HEL cells in vitro, and its underlying mechanisms may involve down-regulation of the HOXB3-mRNA expression.
研究红花注射液对人白血病细胞系HEL增殖和凋亡的影响及其相关分子机制。
用不同浓度的红花注射液处理HEL细胞。未用红花注射液处理的HEL细胞作为对照组。采用MTT法检测不同浓度(10、20、30、40和50 mg/mL)红花注射液处理后24、48和72小时HEL细胞的抑制率。采用流式细胞术检测细胞周期和凋亡情况,并在红花注射液处理(10、20和30 mg/mL)48小时后通过RT-PCR检测HOXB3-mRNA表达。
与对照组相比,不同浓度的红花注射液均以剂量依赖方式抑制HEL细胞增殖(P<0.05)。不同浓度红花注射液处理48小时后,处理组细胞在G2/M期的数量增加,而S期的数量减少,且凋亡率显著高于对照组,呈剂量依赖方式(P<0.05)。与对照组相比,红花注射液处理组细胞中HOXB3-mRNA的表达呈剂量依赖方式降低(P<0.05)。
红花注射液在体外可抑制HEL细胞增殖并诱导其凋亡,其潜在机制可能涉及下调HOXB3-mRNA表达。