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热疗对人胃癌细胞MKN28的细胞周期及节律基因Bmall影响的实验研究 被引量:3

Influence of hyperthermia on cell cycle and rhythm gene Bmall expression in gastric cancer MKN28 cells
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摘要 目的研究加热对胃癌MKN28细胞周期变化是否与节律基因Bmall表达相关,为胃癌择时热疗提供理论依据。方法体外复苏和培养胃癌细胞MKN28;对照组37℃下培养,实验组43qC分别加热0.5h、1.0h和1.5h,用显微镜观察细胞形态变化,采用四甲基偶氮唑盐比色法(MTT)检测细胞增殖抑制率;采用流式细胞术检测细胞周期分布的变化;采用实时定量逆转录一聚合酶链反应(RT-PCR)检测Bmall基因表达变化。结果加热后细胞形态发生显著变化,MTT实验提示37℃加热对细胞生长无明显抑制,细胞43℃热疗0.5h、1.0h和1.5h后细胞抑制率分别为(21.76±4.36)%、(25.30±4.36)%和(27.62±3.78)%,处理后细胞的增殖均受到抑制且抑制趋势具有时间依赖性;流式细胞术显示43℃加热1h后GO^G1最短而G2/M最长,同时实时定量RT-PCR结果显示BmallmRNA表达最低,细胞周期GO-G1变化规律和BmallmRNA变化规律一致。结论热疗可改变胃癌细胞周期及钟基因Bmall表达,提示择时执疗的可行件. Objective To investigate the relationship between the cell cycle blocked by hyperthermia and the expression of rhythm gene Bmall in gastric cancer MKN28 cells so as to provide the academic evidence in hyper- thermia therapy for gastric cancer. Methods The MKN28 cells were resuscitated and cultured in vitro. In control group MKN28 cells were cultivated at 37 ℃. In experimental groups MKN28 cells were heated at 43℃ for different durations. The cell morphology was observed by microscopy. Methylthiazdyl tetrazolium (MTT) assay was adopted to evaluate the inhibitory effect of the cell line. The flow-cytometry was adopted to observe the influence on the cell cycle. The Bmall mRNA expression was investigated by real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR). Results The remarkable changes of cell morphology were observed by microscopy after expo- sure to heating. According to the data of MTT assay, 37 ℃ heating could not inhibit the proliferation of MKN28. The inhibitive rates of cell growth after 0.5 h,1 h,l.5 h at 43 ℃ was (21.76 ±5.46)%,(25.30 ±4.36)% and (27.62 ± 3.78)% , respectively. Results from flow-cytometry showed that GO/G1 phase ceils in lh at 43 ℃ were remarkably less than those in the control group. However G2/M cells were significantly more than those in the control group. The EnRNA expression of Bmall was the lowest when heating lh at 43 ℃ as compared to the control group. Conclusions Hyperthermia could induced the cell cycle changes and the expression of Bmall in gastric cancer MKN28 cells.
出处 《中华物理医学与康复杂志》 CAS CSCD 北大核心 2012年第1期22-25,共4页 Chinese Journal of Physical Medicine and Rehabilitation
关键词 热疗 胃癌MKN28细胞 节律基因Bmall 细胞周期 Hyperthermia Gastric cancer MKN28 cell Rhythm gene Bmall Cell cycle
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  • 1Rampersaud EN, Vujaskovic Z, Inman BA. Hyperthermia as a treatment for bladder cancer. Oncology, 2010, 24:1149-1155.
  • 2Moros EG, Penagaricano J, Novak P, et al. Present and future technology for simultaneous superficial thermoradiotherapy of breast cancer. Int J Hyperthemia, 2010, 26 :699-709.
  • 3Zagar TM, Oleson JR, Vujaskovic Z, et al. Hyperthemia for locally advanced breast cancer. Int J Hyperthermia, 2010, 26 :618-624.
  • 4Hildebrandt B, W ust P, Ahlers 0, et al. The cellular and molecular basis of hyperthermia. Crit Rev Oncol Hematol, 2002,43 :33-56.
  • 5van der Zee J. Heating the patient: a promising approach? Ann Oncol ,2002 ,13: 1173-1184.
  • 6Morrissey JJ, Higashikubo R, Goswami PC, et al. Mild hyperthermia as a potential mechanism to locally enhance cell growth kinetics. J Drug Target, 2009,17:719-723.
  • 7Zhou J, Wang X, Du L, et al. Effect of hyperthermia on the appotosis.
  • 8and proliferation of CaSki cells. Mol Med Reprot ,2011 ,4: 187 -19l.
  • 9Hayashi S, Sakurai H, Hayashi A, et a1. Inhibition of NF -kappa B by combination therapy with parthenolide and hyperthermia and kinetics of apoptosis induction and cell cycle arrest in human lung adenocarcinoma cells. Int J Mol Med ,2010 ,25 :81-87.
  • 10Aravindan N, Shanmugasundaram K, N atarajan M. Hyperthemia induced NFkappaB mediated apoptosis in normal human monocytes. Mol Cell Biochem ,2009 ,327 :29-37.

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  • 1Lee H,Kim S,Choi BH,et al. Hyperthermia improves therapeu-tic efficacy of doxorubicin carried by mesoporous silica nanocon-tainers in human lung cancer cells [ J ]. Int J Hyperthermia,2011,27(7) :698 -707.
  • 2Li SL, Huang CH, Lin CC, et al. Anti tumor effect of BPR-DC-2,a novel synthetic cyclic cyanoguanidine derivative,involvingthe inhibition of MDR-1 expression and down-regulation of p-AKTand PARP-1 in lung cancer[ J]. Invest New Drugs, 2011 , 29(2):195 -206.
  • 3Abe N, Watanabe J,Tsunoda S,et al. Significance of nuclear p-Akt in endometrial carcinogenesis : rapid translocation of p-Aktinto the nucleus by estrogen,possibly resulting in inhibition ofapoptosis[ J]. Int J Gynecol Cancer, 2011,21(2) : 194 - 202.
  • 4Yoshizawa A, Fukuoka J, Shimizu S, et al. Overexpression ofphospho-eIF4E is associated with survival through AKT pathwayin non-small cell lung cancer[ J]. Clin Cancer Res, 2010,16(1):240-248.
  • 5Lou YJ,Jin J,Wang YG.Triptolide inhibits transcription factor NF-kappa B and induces apoptosis of multiplemyeloma cells[J].Leuk Res,2005,29(1):99-105.
  • 6Yang S,Chen J,Guo Z,et al.Triptolide inhibits the growth and metastasis of solid tumors[J].Mol Cancer Ther,2003,2(1):65-72.
  • 7Tang XY,Zhu YQ,Wei B.Synergistic effect of triptolide combined with 5-fluorouracil on colon carcinoma[J].Postgrad Med J,2007,83(979):338-343.
  • 8Jiang XH,Wong BC,Lin MC,et al.Functional p53 is required for triptolide-induced apoptosis and AP-1 and nuclear factor -kappaB activation in gastric cancer cells[J].Oncogene,2001,20(55):8009-8018.
  • 9Phillips PA,Dudeja V,McCarroll JA,et al.Triptolide induces pancreatic cancer cell death via inhibition of heat shock protein 70[J].Cancer Res,2007,67(19):9407-9416.
  • 10Dudeja V,Mujumdar N,Phillips P,et al.Heat shock protein 70 inhibits apoptosis in cancer cells through simultaneous and independent mechanisms[J].Gastroenterology,2009,136(5):1772-1782..

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