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全反式维甲酸和三氧化二砷对人口腔鳞癌细胞系KB细胞周期的影响 被引量:1

Effects of all-trans retinoic acid and arsenic trioxide on cell cycle of oral squamous carcinoma cell line KB
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摘要 目的研究全反式维甲酸(all-trans retinoic acid,ATRA)和三氧化二砷(arsenic trioxide,As2O3)诱导分化对人口腔未分化鳞癌细胞系KB细胞周期的影响及意义。方法采用流式细胞技术观察人口腔未分化鳞癌细胞系KB细胞经不同浓度ATRA和As2O3诱导分化后96h时的细胞周期的变化。结果ATRA作用于KB细胞后,加药组与对照组相比,被阻断在G1期的细胞比率轻度升高,S期比率下降,抑制率随浓度增高无明显升高的趋势。As2O3三个不同浓度作用KB细胞96h时,没有明显改变各细胞周期所占的比例。抑制率随作用浓度的增加而升高。结论ATRA和低浓度As2O3对人口腔未分化鳞癌细胞系KB细胞具有诱导分化作用,ATRA诱导KB细胞分化可能与G1、G0期阻滞有关。 Objective To investigate the change of cell cycle of oral squamous carcinoma cell line KB by employing all-trans retinoic acid (ATRA) and arsenic trioxide (As2O3) and to discuss the significance of such change. Methods The change of cell cycle of oral squamous carcinoma cell line KB when subject to all-trans retinoic acid (ATRA) and arsenic trioxide (As2O3) was detected by flowcytometry. Results The percentage of G1/G0 in KB cells after being subject to all-trans acid (ATRA) for 96 h was higher than that in control group,and the percentage of S was declined. The inhibitory rate did not increase with the increasing concentration of ATRA. The percentage of different phases in KB cells induced by As2O3 for 96 h was not changed. Conclusion All-trans retinoic acid (ATRA) and arsenic trioxide (As2O3) both could induce differentiation of oral squamous cell carcinoma cell line KB. All-trans retinoic acid-induced differentiation of KB cells may be related to G1 arrest.
出处 《北京口腔医学》 CAS 2009年第1期24-26,共3页 Beijing Journal of Stomatology
基金 北京市留学人员科技活动择优资助市优秀项目 北京市卫生局留学回国人员科研专项经费项目 教育部留学回国人员科研启动基金(教外司留[2004]176号)
关键词 全反式维甲酸 三氧化二砷 口腔鳞状细胞癌 细胞周期 All-trans retinoic acid Arsenic trioxide Oral squamous cell carcinoma Cell cycle
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  • 1Beevi SS, Rasheed AM, Geetha A. Evaluation of oxidative stress and nitric oxide levels in patients with oral cavity cancer. Jpn J Clin Onco1,2004,34 ( 7 ) :379-385.
  • 2Kolanjiappan K, Ramachandran CR, Manoharan S. Biochemical changes in tumor tissues of oral cancer patients. Clin Biochem,2003, 36( 1 ) :61-65.
  • 3Kaspar JW, Niture SK, Jaiswal AK. Nrf2 : INrf2 ( Keapl ) signaling in oxidative stress. Free Radic Biol Med, 2009,g7(9) :1304-1309.
  • 4Kuo CC, Liu TW, Chen LT, et al. Combination of arsenic trioxide and BCNU synergistically triggers redox-mediated autophagic cell death in human solid tumors. Free Radio Biol Med,2011,51 (12): 2195 -2209.
  • 5Chien CW,Yao JH, Chang SY, et al. Enhanced suppression of tumor growth by concomitant treatment of human lung cancer cells with suberoylanilide hydroxamic acid and arsenic trioxide. Toxicol Appl Pharmacol, 2011, 257(1 ):59-66.
  • 6Kumar P, Gao Q, Ning Y, et al. Arsenic trioxide enhances the therapeutic efiqcacy of radiation treatment of oral squamous carcinoma while protecting bone. Mol Cancer Ther, 2008,7 (7) :2060-2069.
  • 7Le A, Cooper CR, Gouw AM, et al. Inhibition of lactate dehydrogenase A induces oxidative stress and inhibits tumor progression. Proc Natl Acad Sci USA, 2010,107 ( 5 ) :2037-2042.
  • 8Jaiswal AK. Nrf2 signaling in coordinated activation of antioxidant gene expression. Free Radic Biol Med,2004,36(10) :1199-1207.
  • 9Chen XL,Kunsch C. Indction of cytoprotective genes through Nri2/ antioxidant response element pathway: a new therapeutic approach for the treatment of inflammatory diseases. Curt Pharm Des, 2004, 10 (8) :879-891.
  • 10Hybertson BM, Gao B, Bose SK, et al. Oxidative stress in health and disease: the therapeutic potential of Nrt2 activation. Mol Aspects Med ,2011,32(4-6) :234-246.

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