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索拉非尼联合热疗不同联合方案对肝癌HepG-2细胞增殖抑制的影响

Inhibitory Effect of Sorafenib Combined with Hyperthermia on the Proliferation of Human Hepatocellular Carcinoma Cells Line HepG-2
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摘要 目的探讨索拉非尼(Sorafenib)联合热疗(hyperthermia)不同联合方案对肝癌HepG-2细胞增殖抑制的影响。方法索拉非尼及热疗单独、同时、序贯联合后以MTT法测定HepG-2细胞增殖。结果索拉非尼和热疗均对肝癌HepG-2细胞增殖抑制作用(P〈0.01),同时应用具有协同作用(P〈0.01);索拉非尼先用组与热疗先用组相比疗效相似(P〉0.05),同时联合组高于序贯联合组(P〈0.01),联合组及序贯用药组均优于索拉非尼及热疗单用组。联合组均高于单独应用组(P〈0.01)。结论索拉非尼和热疗对肝癌HepG-2细胞均有增殖抑制作用,索拉非尼联合热疗具有协同作用。 Objective To observe the inhibitory effect on the Proliferation of HepG-2 cells by the treatment of sorafenib combined with hyperthermia. Methods The Proliferation of HepG-2 cells was determined by MTT assy after administration with sorafenib alone, hyperthermia alone or sorafenib in combination with hyperthermia. Results Either sorafenib or hyperthermia had an inhibitory effect on HepG-2 cells and sorafenib combined with hyperthermia revealed a synergistic effect (P〈0.01). The efficacy in patients receiving sequential chemotherapy with sorafenib was similar to that in patients receiving sequential chemotherapy with hyperthermia (P〉0.05). The inhibitory effect was higher in the dual-therapy group than in the monotherapy groups (P〈0.01). The inhibitory effect was higher in sorafenib combined with hyperthermia than the sequential chemotherapy (P〈0.01). Conclusions Sorafenib or hyperthermia alone has an inhibitory effect on the proliferation of HepG-2 cells. Simultaneous administration with sorafenib and hyperthermia has a synergistic effect. Sequential chemotherapy is higher than the sorafenib or hyperthermia alone.
作者 丁素银 肖广显 丁素静 程英俊 DING Su-yin, XIAO Guang-xian, DING Su-jing, CHENG Ying-jun (1.Internal Oncology Department, Baoding Hengxing Hospital of Integrated Traditional and Western medicine, Baoding 071000; 2. Department of Emergency, the 252nd Hospital of PLA, Baoding 071000, China)
出处 《医学信息》 2011年第15期5003-5004,共2页 Journal of Medical Information
关键词 索拉非尼 热疗 肝癌HEPG-2细胞 增殖 Sorafenib Hyperthermia Human Hepatocellular Carcinoma(HepG2 Cell) Proliferation
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参考文献6

  • 1Joseph L, Roti R. Cellular responses to hyperthermia (40C-46C): Cell killing and molecular events[J1. Int J Hyperthermia, 2008,24(1) : 3 - 15.
  • 2lliakisy G, Kriegy T, Gnanz J, et al. Evidence for an S-Phage check point regulating DNA replication after heat shock: a review [J]. Int J Hyperthermia, 2004,20(2) : 240-249.
  • 3Strumberg D, Clark JW, Schwartz B, et al. Safety, pharmacokinetics, and pre- liminary antitumor activity of sorafenib: a review of four phage 1 trial in patients with advanced refractory solid tumors[J]. Oncologist, 2007,12(4) : 426-437.
  • 4Wilhelm SM, Carter C, Tang L, et al. BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor ty- rosine kinases involved in tumor progression and angiogenesis [J]. Cancer Res, 2004,64(19) : 7099-7109.
  • 5隋忠国,薛宏伟,荆凡波,冷萍.索拉非尼联合卡培他滨治疗肝细胞癌患者的临床研究[J].中国药房,2008,19(11):848-849. 被引量:20
  • 6陈逢生,崔彦芝,罗荣城,李爱民,伍婧,张华.索拉非尼与顺铂的不同联合方案对肝癌HepG2细胞的作用研究[J].实用医学杂志,2008,24(7):1096-1098. 被引量:3

二级参考文献12

  • 1Patt Z, Hassan MM, Aguay A, et al. Oral capecitabine for the treatment of hepatocellar carcinoma, cholangiocarcinoma, and gallbladdercarcinoma [J] . Cancer, 2004, 101 (3) :578.
  • 2DeVita VT Jr, Abou - Alfa GK.Therapeutic implica- tions of the new biology[J] .Cancer J, 2000, 6(Suppl 2).113.
  • 3Wilhelm SM, Carter C, Tang L, et al. BAY 43- 9006 exhibits broad spectrum oral anti - tumor activity and targets the Raf/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis[J ]. Cancer Res, 2004,64(19) : 7 099 .
  • 4Ghassan K, Abou- Alfa GK, Lawrence S, et al. Phase Ⅱ study of sorafenib in patients with advanced hepatocellular carcinoma[J] .J Clin Oncol, 2006, 24(26): 4 293.
  • 5Yeo W, Mok TS, Zee B, et al. Arandomized phase Ⅲ study of doxorubicin versus cisplatin/ interferon alpha- 2b/doxorubicin/fluorouracil (PIAF) combination themotherapy for unresectable hepatocellular carcinoma[J ]. J Natl Cancer Inst , 2005,97(20). 1 532.
  • 6Richly H, Kupsch P, Passage K, et al.Results of a phase Ⅰ trial of BAY 43 - 9006 in combination with doxorubicin in patients with primary hepatic cancer[J ]. Int J Clin Pharmacol Ther, 2004,42(11) : 650.
  • 7Strumberg D, Richly H, Hilger RA, et al. Phase Ⅰ clinical and pharmacokinetic study of the novel raf kinase and vascular endothelial growth factor receptor inhibitor BAY 43- 9006 in patients with advanced refractory solid tumors[J] .J Clin Oncol , 2005,23(5) :965.
  • 8Falcone A, Ricci S, Brunetti I, et al. Phase Ⅲ trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan(FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinoteean (FOLFIRI) as first-line treatment for metastatic coloreetal cancer: the Gruppo Oncologico Nord Ovest [J]. J Clin Oncol,2007,25 (13) : 1670-1676.
  • 9Wilhelm S M, Carter C, Tang L, et al. BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis [ J ]. Cancer Res, 2004,64 (19) : 7099-7109.
  • 10Jane E P, Premkumar D R, Pollack I F. Coadministration of sorafenib with rottlerin potently inhibits cell proliferation and migration in human malignant glioma cells [J]. J Pharmacol Exp Ther,2006,319(3) : 1070-1080.

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