期刊文献+

冬凌草甲素联合卡培他滨对人乳腺癌MDA-MB-231细胞增殖的影响 被引量:10

Effects of Oridonin combined with Capecitabine on the proliferaction of MDA-MB-231 human breast cancer cens
原文传递
导出
摘要 目的观察冬凌草甲素联合卡培他滨对乳腺癌MDA-MB-231细胞增殖的影响。方法观察不同浓度(10、20及40μmol/L)的冬凌草甲素和卡培他滨及其两者联合用药与MDA-MB-231细胞孵育24和48h的细胞存活率。考察5μmol/L的冬凌草甲素和卡培他滨及其两者联合使用对MDA。MB-231细胞集落形成的影响。考察20μmol/L的冬凌草甲素和卡培他滨及其两者联合使用对MDA-MB-231细胞核形态,细胞周期及凋亡的影响。结果冬凌草甲素和卡培他滨在20μmol/L孵育48h对MDA-MB-231细胞的抑制率分别为49.5%和58.6%,而将两者联合使用时,对肿瘤的抑制率达到94.6%。联合给药后肿瘤集落形成的大小和个数较单独给药时明显减少(P〈0.01)。同时给予冬凌草甲素和卡培他滨,可将细胞同时阻滞于S期和G2/M期,凋亡细胞的比例也有显著升高(P〈0.01)。结论将冬凌草甲素与卡培他滨联合给药之后,两者可以协同起效,共同发挥抗肿瘤效果,对乳腺癌MDA-MB-231细胞的增殖起到显著的抑制作用。 Objective To investigate the effects of oridonin combined with capecitabine on the proliferaction of MDA-MB-231 human breast cancer ceils. Methods Effect of different concentrations ( 10, 20 and 40 μmol/L)of oridonin, capecitahine and their combination on the proliferation of MDA-MB-231 celts after incubation for 24 or 48 h was studied. Then, the effect of 5 μmol/L of oridonin, capecitabine and their combination on cell colony formation was detected. Finally, influence of 20 μmol/L of oridonin, capecitabine and their combination on morphological alteration of nucleus, cell cycle and apoptosis was explored. Results The inhibition rate on MDA-MB-231 cells after incubation with 20 μmoL/L oridonin or capecitabine for 48 h was 49. 5% and 58.6%, respectively, while the inhibition rate against proliferation of MDA-MB-231 cells reached 94. 6% with combination of 20 txmol/L oridonin and capecitabine. Cells incubated with combination of oridonin and capecitabine formed fewer and smaller colonies ( P 〈 0. 01 ). Meanwhile, cells in the combination group arrested at S and G2/M phases at the same time, and combination of two drugs caused more apoptotic ceils ( P 〈 0. 01 ). Conclusion Oridonin combined with capeeitabine can synergistically inhibit the proliferation of MDA-MB-231 human breast cancer cells.
出处 《中华医学杂志》 CAS CSCD 北大核心 2017年第46期3647-3651,共5页 National Medical Journal of China
关键词 冬凌草甲素 卡培他滨 抗肿瘤 乳腺癌 细胞周期 Oridonin Capecitabine Antitumor Breast cancer Cell cycle
  • 相关文献

参考文献2

二级参考文献24

  • 1姜丽娜,于世英,熊慧华,张孟贤.胸苷磷酸化酶在癌组织中表达的研究[J].中华肿瘤杂志,2004,26(5):297-299. 被引量:72
  • 2Tan W, Lu J, Huang M, et al. Anti-cancer natural products isolated from Chinese medicinal herbs[J]. Chin Med, 2011, 6(1): 27.
  • 3Huang J, Wu L, Ikejima T. Reactive oxygen species mediate orido- nin-induced HepG2 apoptosis through p53, MAPK, and mitochon- drial signaling pathways[J]. J Pharmacol Sci, 2008, 107(4): 370-379.
  • 4Cheng Y, Qiu F, Ye YC, et al. Oridonin induces G2/M arrest and apoptosis via activating ERK-p53 apoptotie pathway and inhibiting PTK-RAS-RAFJNK survival pathway in murine fibrosarcoma L929 cells[J]. Arch Biochem Biophys, 2009, 490(1): 70-75.
  • 5Gao FH, Hu XH, Li W, et al. Oridonin induces apoptosis and senes- cence in colorectal cancer cells by increasing histone hyperacety- lation and regulation of p16, p21, p27 and c-myc[J]. BMC Cancer, 2010, 10: 610.
  • 6Bu HQ, Liu DL, Wei WT, et al. Oridonin induces apoptosis in SW1990 pancreatic cancer cells via p53- and caspase-dependent induction of p38 MAPK[J]. Oncol Rep, 2014, 31(2): 975-982.
  • 7Harikumar KB, Kunnumakkara AB, Sethi G, et al. Resveratrol, a multitargeted agent, can enhance antitumor activity of gemcitabinc in vitro and in orthotopic mouse model of human pancreatic cancer [J]. Int J Cancer, 2010, 127(2): 257-268.
  • 8Stathis A, Moore MJ. Advanced pancreatic carcinoma: current treat- ment and future challenges[J]. Nat Rev Clin Oncol, 2010, 7(3): 163- 172.
  • 9Maitra A, Hruban RH. Pancreatic Cancer[J]. Annu Rev Pathol, 2008, 3: 157-188.
  • 10Guo Y, Shan Q, Gong Y, et al. Oridonin in combination with ima- tinib exerts synergetic anti-leukemia effect in Ph + acute lympho- blastic leukemia cells in vitro by inhibiting activation of LYN/ mTOR signaling pathway[J]. Cancer Biol Ther, 2012, 13(13): 1244- 1254.

共引文献24

同被引文献57

引证文献10

二级引证文献48

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部