您的位置: 首页 > 2020年3月 第51卷 第2期 > 文字全文
2023年7月 第38卷 第7期11
目录

吴茱萸碱通过阻滞细胞周期而抑制人骨肉瘤细胞增殖

Evodiamine inhibits proliferation of human osteosarcoma cells by arresting the cell cycle

来源期刊: 广州医药 | 10-14 发布时间:2021-11-28 收稿时间:2025/11/13 17:51:52 阅读量:34
作者:
关键词:
吴茱萸碱人骨肉瘤HOS细胞增殖细胞周期
EvodiamineHuman osteosarcoma HOS cellsProliferationCell cycle
DOI:
10.3969/j.issn.1000-8535.2020.02.003
收稿时间:
2019-11-01 
修订日期:
 
接收日期:
 
引用总数:
0  
目的 体外细胞实验检测吴茱萸碱对骨肉瘤HOS细胞株细胞周期及体外增殖能力的影响。方法 通过利用浓度为0、3、6、12 μmol/L吴茱萸碱处理骨肉瘤HOS细胞48 h后,Hoechst-33258荧光染色观察不同浓度吴茱萸碱处理后HOS细胞核的形态学变化。利用流式细胞术检测3 μmol/L的吴茱萸碱处理后骨肉瘤HOS细胞的细胞周期分布变化。结果 3、6、12 μmol/L的骨肉瘤吴茱萸碱处理细胞,细胞呈现凋亡核碎裂等典型变化,而且随药物剂量增加而更趋明显。呈剂量依赖性抑制其体外增殖能力。3 μmol/L吴茱萸碱处理骨肉瘤HOS细胞0、24、48、72 h,各组细胞周期变化如下:G0/G1期:对照组(51.12±2.13)%、24 h(19.17±1.02)%、48 h(16.94±1.67)%、72 h(11.05±1.25)%;S期:对照组(32.92±0.73)%、24 h(31.00±1.42)%、48 h(32.38±3.03)%、72 h(29.18±2.87)%;G2/M期:对照组(16.01±2.26)%、24 h(49.82±0.62)%、48 h(50.6767±2.80)%、72 h(59.56±1.97)%。结论 吴茱萸碱可诱导人骨肉瘤HOS细胞发生G2/M期阻滞,而S期变化不明显。说明吴茱萸碱可以抑制骨肉瘤细胞的增殖能力,并阻滞细胞周期于G2/M期。
Objective Using transcriptome sequencing and in vitro cell assay to detect the effect of evodiamine on cell cycle and proliferation in osteosarcoma HOS cell line. Methods HOS cells were treated with evodiamine at 0, 3, 6, and 12 μmol/L for 48 hours, Hoechst-33258 fluorescence staining was used to observe the morphological changes of HOS nuclei after treatment with different concentrations of evodiamine.The cell cycle distribution of HOS cells treated with 3 μmol/L evodiamine was detected by flow cytometry. Results 3,6,12 μmol/L osteosarcoma treated with evodiamine, the cells showed typical changes such as apoptotic nuclear fragmentation, and it became more obvious with the increase of drug dosage. Inhibition of proliferation in vitro in a dose-dependent manner.HOS cells were treated with 3 μmol/L evodiamine for 0, 24, 48, 72 h. The cell cycle changes of each group were as follows: G0/G1 phase: control group(51.12±2.13)%, 24 h(19.17±1.02)%, 48 h(16.94±1.67) %, 72 h(11.05±1.25)%;S phase: control group(32.92±0.73)%, 24 h(31.00±1.42)%, 48 h(32.38±3.03)%, 72 h(29.18±2.87)%;G2/M period: control group(16.01±2.26)%, 24 h(49.82±0.62)%, 48 h(50.6767±2.80)%, 72 h(59.56±1.97)%. Conclusion Analysis of the above results revealed that evodiamine can induce G2/M phase arrest in human osteosarcoma HOS cells, but the S phase changes are not obvious. It indicated that evodiamine would inhibit the proliferation of osteosarcoma cells and block the cell cycle in G2/M phase.
1、 张庆然,周昭伶,潘振海,等. 吴茱萸碱抑制Huh7细胞生长并增强细胞对TRAIL的敏感性[J]. 中国病理生理杂志,2018,34(2) :212-217. 张庆然,周昭伶,潘振海,等. 吴茱萸碱抑制Huh7细胞生长并增强细胞对TRAIL的敏感性[J]. 中国病理生理杂志,2018,34(2) :212-217.
2、 LIAO C H, PAN S L, GUH J H, et al. Antitumor mechanism of evodiamine, a constituent from Chinese herb Evodiae fructus, in human multiple-drug resistant breast cancer NCI/ADR-RES cells in vitro and in vivo[J]. Carcinogenesis,2005,26(5):968-975. LIAO C H, PAN S L, GUH J H, et al. Antitumor mechanism of evodiamine, a constituent from Chinese herb Evodiae fructus, in human multiple-drug resistant breast cancer NCI/ADR-RES cells in vitro and in vivo[J]. Carcinogenesis,2005,26(5):968-975.
3、 KAN S F, YU C H, PU H F, et al. Anti-proliferative effects of evodiamine on human prostate cancer cell lines DU145 and PC3[J]. J Cell Biochem,2007(101):44-56. KAN S F, YU C H, PU H F, et al. Anti-proliferative effects of evodiamine on human prostate cancer cell lines DU145 and PC3[J]. J Cell Biochem,2007(101):44-56.
4、 吕艳伟,郭星娴,周鹏,等. 吴茱萸碱结肠癌细胞自噬抑制其增殖的研究[J]. 中草药,2018(20):4851-4856. 吕艳伟,郭星娴,周鹏,等. 吴茱萸碱结肠癌细胞自噬抑制其增殖的研究[J]. 中草药,2018(20):4851-4856.
5、 徐俊杰,杨然,杨芳景,等. 吴茱萸碱抗肿瘤机制的研究进展[J]. 上海交通大学学报,2018,38(5):578-583. 徐俊杰,杨然,杨芳景,等. 吴茱萸碱抗肿瘤机制的研究进展[J]. 上海交通大学学报,2018,38(5):578-583.
6、 HONG J Y,PARK S H,MIN H Y,et al. Anti-proliferative effects of evodiamine in human lung cancer cells[J]. J Cancer Prev,2014,19(1):7-13. HONG J Y,PARK S H,MIN H Y,et al. Anti-proliferative effects of evodiamine in human lung cancer cells[J]. J Cancer Prev,2014,19(1):7-13.
7、 周鹏,吕艳伟,李静,等. 吴茱萸碱通过NF-κB-p65信号通路抑制人结肠癌细胞SW480的迁移和侵袭[J]. 第三军医大学学报,2019,41(6):549-555. 周鹏,吕艳伟,李静,等. 吴茱萸碱通过NF-κB-p65信号通路抑制人结肠癌细胞SW480的迁移和侵袭[J]. 第三军医大学学报,2019,41(6):549-555.
8、 张涵妮,祝文浩,王慧茹,等. 吴茱萸碱对人胃癌BGC-823细胞增殖的影响及分子机制研究[J]. 亚太传统医药,2019(4):19-23. 张涵妮,祝文浩,王慧茹,等. 吴茱萸碱对人胃癌BGC-823细胞增殖的影响及分子机制研究[J]. 亚太传统医药,2019(4):19-23.
9、 WHELAN J, PATTERSON D, PERISOGLOU M, et al. The role of interferons in the treatment of osteosarcoma[J]. Pediatr Blood Cancer, 2010, 54(3):350-354. WHELAN J, PATTERSON D, PERISOGLOU M, et al. The role of interferons in the treatment of osteosarcoma[J]. Pediatr Blood Cancer, 2010, 54(3):350-354.
10、 MEYERS P A, SCHWARTZ C L, KRAILO M D, et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival--a report from the Children's Oncology Group[J]. J Clin Oncol, 2015, 26(4):633-638. MEYERS P A, SCHWARTZ C L, KRAILO M D, et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival--a report from the Children's Oncology Group[J]. J Clin Oncol, 2015, 26(4):633-638.
11、 DHAMMI I K, KUMAR S. Osteosarcoma: A journey from amputation to limb salvage[J]. Indian J Orthop, 2014, 48(3):233-234. DHAMMI I K, KUMAR S. Osteosarcoma: A journey from amputation to limb salvage[J]. Indian J Orthop, 2014, 48(3):233-234.
12、 OTTAVIANI G, JAFFE N. The etiology of osteosarcoma[J]. Cancer Treat Res, 2009, 152(152):15-32. OTTAVIANI G, JAFFE N. The etiology of osteosarcoma[J]. Cancer Treat Res, 2009, 152(152):15-32.
13、 MIRABELLO L, TROISI R J, SAVAGE S A. International osteosarcoma incidence patterns in children and adolescents, middle ages and elderly persons[J]. Int J Cancer, 2010, 125(1):229-234. MIRABELLO L, TROISI R J, SAVAGE S A. International osteosarcoma incidence patterns in children and adolescents, middle ages and elderly persons[J]. Int J Cancer, 2010, 125(1):229-234.
14、 KAGER L, ZOUBEK A, DOMINKUS M, et al. Osteosarcoma in very young children: experience of the Cooperative Osteosarcoma Study Group[J]. Cancer, 2010, 116(22):5316-5324. KAGER L, ZOUBEK A, DOMINKUS M, et al. Osteosarcoma in very young children: experience of the Cooperative Osteosarcoma Study Group[J]. Cancer, 2010, 116(22):5316-5324.
15、 DORFMAN H D, CZERNIAK B. Bone cancers[J]. Cancer, 2015(75):203-210. DORFMAN H D, CZERNIAK B. Bone cancers[J]. Cancer, 2015(75):203-210.
上一篇
下一篇
出版者信息








《广州医药》公众号
目录