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热化疗对K562细胞体外增敏作用的实验研究 被引量:2

Thermotherapy enhances the sensitivity of K562 to chemotherapy in vitro:An experimental study
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摘要 目的观察热疗联合阿霉素对人慢性白血病细胞株K562细胞内的药物浓度变化及凋亡的影响。方法MTT法确定阿霉素的工作浓度,以该浓度进行化疗或与热疗的联合,选择温度40、41、42℃,体外作用于K562细胞。作用前及作用48h采用台盼蓝拒染法检测肿瘤细胞的存活率;MTT法检测肿瘤细胞增殖的抑制作用;流式细胞仪检测肿瘤细胞的凋亡及细胞内药物浓度的变化。观察热疗联合阿霉素的抗肿瘤效果。结果作用48h IC50的药物浓度作为实验的工作浓度。热化疗组对K562细胞有明显的抑制作用(P<0.01),随着温度的增高而增强;热化疗组细胞内的药物浓度明显增加(P<0.01)。结论热疗联合阿霉素能增加K562细胞内的药物浓度,提高肿瘤细胞的凋亡率。 Objective To observe the effect of thermotherapy on the intraeellular adriamycin concentration and apoptosis of K562 cells in vitro. Methods The working concentration of adriamycin against K562 was determined by MTT assay. K562 cells were subjected to thermotherapy (at 40℃, 41℃, 42℃) and chemotherapy with adriamycin alone or in conjunction, and the cell survival rates were determined at 48h after the treatment. The cell growth inhibition effect of the treatment was evaluated with MTT assay, and the apoptosis rates of K562 and alteration of intracellular adriamycin eoneentration were determined by flow cytometrie analyses. Results The IC50 of adriamycin was defined as its working concentration in the experiment. The thermotherapy at 40,41 and 42℃ for 60 rain in conjunction with chemotherapy significantly inhibited the growth of K562 cells (P〈0.01). The results of flow cytometric analyses showed that thermotherapy and adriamycin chemotherapy, used either alone or in conjunction, obviously increased the apoptosis rates of K562 cells(P〈0.01) and thermotherapy remarkably increased the intracellular concentration of adriamycin. Conclusion Adriamycin chemotherapy combined thermotherapy for 60min can increase the intracellular concentration of adriamycin and the apoptosis rates of K562 cells.
出处 《实用医药杂志》 2008年第12期1497-1499,1502,共4页 Practical Journal of Medicine & Pharmacy
关键词 热化疗 阿霉素 K562 增敏作用 细胞凋亡 Thermo-chemo-therapy Adriamycin K562 cells Sensitization Apoptosis
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  • 1吕永钢,刘静.基于肿瘤靶向热疗的磁性微/纳米颗粒研究进展[J].微纳电子技术,2004,41(9):22-28. 被引量:18
  • 2何跃明,吕新生,艾中立,刘志苏,王平康.磁介导热疗联合顺铂化疗对肝癌细胞的影响及其机制[J].中华实验外科杂志,2004,21(10):1170-1172. 被引量:17
  • 3邢宝玲,张东生.纳米As_2O_3磁性脂质体的制备及表征[J].南京医科大学学报(自然科学版),2005,25(1):9-13. 被引量:14
  • 4van der Zee J. Heating the patient : a promising approach. Ann Oncol, 2002,13(8) : 1173-1184.
  • 5Takahashi I, Emi Y, Hasuda S, et al. Clincal application of hyperthernfia combined with anticancer drugs for the treatment of solid tumors. Surgery, 2002,131 (1 Suppl) : S78-S84.
  • 6Westermann AM, Grosen EA, Katschinski DM, et al. A pilot study of whole body hyperthermia and carboplatin in platinum-resistant ovarian cancer. Eur J Cancer, 2001, 37(9) : 1111-1117.
  • 7Rietbroek RC, van de Vaart PJ, Haveman J, et al. Hyperthermia enhances the cytotoxicity and platinum-DNA adduct formation of lobaplatin and oxaliplatin in cultured SW1573 cells. J Cancer Res Clin Oncol, 1997, 123(1): 6-12.
  • 8Hirohashi Y, Hidaka K, Sato S, et al. Biomodulation by hyperthermia of topoisomeraes II-targeting drug in human colorectal cancer cells. Jpn J Cancer Res, 1995, 86(11): 1097-1105.
  • 9Van Heek-Romanowski R, Putter S, Trarbach T, et al. Etoposide toxicity on human neuroblastoma cells in vitro is enhanced by preceeding hyperthermia. Med Pediatr Oncol,2001,36( 1 ) : 197-198.
  • 10Kondo T, Ueda K, Kano E. Combined effects of hyperthermia and CPT-11 on DNA strand breaks in mouse rnmammry carcinoma FM3A cells. Anticancer Res, 1995,15 ( 1 ) : 83-86.

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  • 1蒋东,李芳,沈文明,郑世营.热疗对肺癌A549细胞周期和凋亡的影响[J].南通大学学报(医学版),2008,28(3):172-174. 被引量:3
  • 2Rong Y,Mack P.Apoptosis induced by hyperthermia in Dunn osteosarcoma cell line in vitro[J].Int J Hyperthermia,2000,16 (1):19-27.
  • 3Saga T,Sakahara H,Nakamoto Y,et al.Enhancement of the therapeutic outcome of radio immunotherapy by combinati on with who-bodymild hyperthermia[J].Eur J Cancer,2001,37(11):1429-1434.
  • 4Sawaji Y,Sato T,Taakeuchi A,et al.Anti-angiogenic action of hyperthermia by suppressing gene expressi on and production of tumour-derived vascular endothelial growth factor in vivo and invitro[J].Br J Cancer,2002,86(10):1597-1603.
  • 5Kanaya Y,Doihara H,Shiroma K,et al.Effect of combined therapy with the antiestrogen agent toremifene and local hyperthermia on breast cancer cells implanted in nude mice.[J].Surg Today,2008,38(10):911-920.
  • 6Haegerstrand A,Huang YH,Frostegard J.Effects of in vitro hyperthermia on proliferative responses and lymphocyte activity[J].Clin Exp Immunol,1996,103(1):61-66.
  • 7Deezagi A,Manteghi S,Khosravani P,et al.Induced apoptosis by mild hyperthermia occurs via telomerase inhibition on the three human myeloid leukemia cell lines:TF-1,562,and HL-60[J].Leuk Lymphoma,2009,50(9):1519-1520.
  • 8Klostergaard J, Leroux ME, Auzenne E, et al. Hyperthermia engages the intrinsic apoptotic pathway by enhancing up- stream caspase activation to overcome apoptotic resistance in MCF-7 breast adenocarcinoma cells [ J ]. J Cell Biochem, 2006,98(2) :356 -369.
  • 9Peer A J, Grimm MJ, Zynda ER, et al. Diverse immune mechanisms May contribute to the survival benefit seen in cancer patients receiving hyperthermia [ J ]. Immunol Res, 2010,46( 1 - 3 ) : 137 - 154.
  • 10Zhao PJ, Jiang H, Su D, et al. Inhibition of cell proliferation by mild hyperthermia at 43 degrees C with Paris Saponin I in the lung adenocarcinoma cell line PC-9 [ J ]. Mol Med Rep,2015,11(1) :327 -332.

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