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β-榄香烯联合顺铂对乳腺癌MCF-7细胞增殖和凋亡的影响
引用本文:王传疆,王雷,胡海地. β-榄香烯联合顺铂对乳腺癌MCF-7细胞增殖和凋亡的影响[J]. 现代肿瘤医学, 2014, 0(5): 1001-1004
作者姓名:王传疆  王雷  胡海地
作者单位:中国医科大学附属第一医院血管甲状腺外科,辽宁沈阳110001
基金项目:国家自然科学基金资助项目(编号:81000136)
摘    要:目的:探讨β-榄香烯联合顺铂对乳腺癌MCF-7细胞生长的影响。方法:体外培养乳腺癌MCF-7细胞,将β-榄香烯(浓度梯度为25、50、100、150、200μg/ml),单独作用于乳腺癌MCF-7细胞,加药24h、48h后用噻唑蓝(MTT法)法检测细胞增殖情况。用流式细胞术检测用药24h后对MCF-7细胞凋亡和细胞增殖周期的影响,选取合适的药物浓度(β-榄香烯125μg/ml),与顺铂(3μg/ml)进行联合用药。加药24h、48h用MTT法检测细胞增殖情况,用流式细胞术检测24h后药物组对MCF-7细胞凋亡和细胞增殖周期的影响。结果:MTT法结果显示β-榄香烯单独用药24h、48h后,与对照组相比,实验组乳腺癌MCF-7细胞的抑制率高于对照组(P<0.05),并且在一定程度上呈浓度和时间依赖性。联合用药时,细胞的抑制率和凋亡率要显著高于单独用药(P<0.01)。与对照组相比,榄香烯能够使MCF-7细胞产生明显的G0/G1期阻滞(P<0.01)。结论:β-榄香烯单独或与顺铂联合作用均能抑制MCF-7细胞的增殖,促进其凋亡,且β-榄香烯联合顺铂的作用要显著高于单独用药组,β-榄香烯和顺铂可协同(CDI<1)促进MCF-7细胞凋亡,其机制可能与G0/G1期阻滞有关。

关 键 词:β-榄香烯  顺铂  MCF-7细胞  增殖  凋亡  细胞周期

ING4 - induced S phase early stage arrest in thyroid cancer cells SW579 and its mecha-nism
Wang Chuanjiang,Wang Lei,Hu Haidi. ING4 - induced S phase early stage arrest in thyroid cancer cells SW579 and its mecha-nism[J]. Journal of Modern Oncology, 2014, 0(5): 1001-1004
Authors:Wang Chuanjiang  Wang Lei  Hu Haidi
Affiliation:( Division of Vascular and Thyroid Surgery,First Hospital of China Medical University,Liaoning Shenyang 110001 ,China)
Abstract:Objective:To study the effects and mechanisms of ING4 on cell cycle of thyroid cancer cell SW579. Methods:The Proliferative ratio of SW579 cells after treated with ING4 was detected by soft agarose assay. We detec-ted the changes of cell cycle after treated with ING4 by PI staining and Cldu/ Idu double staining. The cell cycle relat-ed Proteins were analyzed by Western blot. Results:ING4 could inhibit the Proliferation and induced S Phase early stage arrest in SW579 cells. The levels of cell cycle related Proteins,P53,PhosPho - S345 - Chk1 and PhosPho - T68- Chk2,were higher in treated cells than untreated ones. Conclusion:ING4 could induce S early stage arrest in SW579 cell,uP - regulate P53 exPression and cell cycle related Proteins. eowever,the relationshiP among ING4,P53 and cell cycle related Proteins by activating P53 exPression was needed further studies.
Keywords:SW579 cells  ING4  S Phase  Proliferation  P53
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