期刊文献+

口腔鳞状细胞癌体内生长的昼夜生物节律特征 被引量:1

Circadian rhythm of oral squamous cell carcinoma in vivo
暂未订购
导出
摘要 目的:探讨口腔鳞状细胞癌体内生长的昼夜生物节律改变特征。方法:32只裸鼠置于12 h光照、12 h黑暗交替的环境中,将人颊鳞状细胞癌BcaCD885细胞接种于裸鼠颊部,建立颊鳞状细胞癌模型,3周后在24 h内,按灯亮后4、10、16、22 h 4个时间点分别处死8只裸鼠时间以开灯后的小时数为参考(hours after light onset,HALO),即4 HALO、10HALO、16HALO、22HALO。取出肿瘤测量体积,用流式细胞仪测定肿瘤细胞的增殖指数(proliferation index,PI)和凋亡指数(apoptosis index,AI)。用余弦分析法检验肿瘤体积、肿瘤细胞PI和AI是否具有昼夜节律性,用方差分析各指标在4个时间点差异的显著性。结果:肿瘤体积和肿瘤细胞PI具有明显的昼夜节律变化特征,肿瘤体积在不同时间点的差异具有统计学意义,肿瘤体积的峰值和谷值分别出现在3.23HALO、15.23HALO,肿瘤细胞PI的峰值和谷值分别出现在6.60HALO、18.16HALO。肿瘤细胞的AI无昼夜节律性,但在不同时间点差异具有统计学意义。结论:体内生长的口腔鳞状细胞癌的细胞增殖活性和肿瘤体积具有昼夜节律变化特点,肿瘤体积和细胞AI在昼夜不同时间点差异变化较大。 Objective:To investigate the change of circadian rhythm in oral squamous cell carcinoma(OSCC)in vivo.Methods:Totally 32 nude mice were maintained in 12 h light alternating with 12 h dark.Human oral squamous cell carcinoma cell line BcaCD885 was transplanted subcutaneously into nude mice cheeks to develop an OSCC animal model.Mice were sacrificed at 4 different time points 4,10,16,22 h(4 hours after light onset(HALO),10HALO,16HALO,22HALO)of 24 h 3 weeks after transplantation,with 8 mice of each group.Tumors were dissected away and tumor sizes were measured.Tumor cell proliferation index(PI)and apoptosis index(AI) were determined by flow cytometry.Cosine analysis was used to detect circadian rhythm of tumor size,tumor cell PI and AI.Variance of significant difference in the four time groups was tested by ANOVA.Results:Tumor size and tumor cell PI exhibited significant circadian rhythm.Tumor sizes had significant differences at indifferent time points.Peak and trough values of tumor size appeared at 3.23HALO and 15.23HALO,respectively.Peak and trough values of tumor cell PI appeared at 6.60HALO and 18.16HALO,respectively.AI of tumor cells showed no circadian rhythm,but the differences of different time points were significant.Conclusions:Cell proliferation and tumor size of OSCC in vivo show circadian rhythm.Tumor size and AI have significant differences at different time points.
出处 《重庆医科大学学报》 CAS CSCD 北大核心 2013年第7期770-773,共4页 Journal of Chongqing Medical University
关键词 口腔 鳞状细胞 生物节律 增殖 凋亡 oral cavity carcinoma squamous cell circadian rhythm proliferation apoptosis
  • 相关文献

参考文献9

  • 1Eismann E A,Lush E,Sephton S E.Circadian effects in cancer-rel- evant psychoneuroendocrine and immune pathways[J].Psychoneuroen- docrinology, 2010,35 (7) : 963-976.
  • 2Huang X L, Fu C J, Bu R F.Role of circadian clocks in the devel- opment and therapeutics of cancer[J].J Int Med Res, 2011,39 (6) : 2061 - 2066.
  • 3Jasser S A, Blask D E,Brainard G C.Light during darkness and can- eer:relationships in circadian photoreception and tumor biology[J].Can- eer Causes Control,2006,17(4) :515-523.
  • 4Fu L,Lee (2 C.The circadian cloek:paeemaker and tumor suppres- sor[J].Nat Rev Cancer, 2003,3 (5) : 350-361.
  • 5Filipski E, L:vi F.Cireadian disruption in experimental eancer pro- cesses[J].Integr Cancer Ther, 2009,8 (4) : 298-302.
  • 6童建.余弦分析法在生物节律研究中的应用[J].中国卫生统计,1991,8(1):23-25. 被引量:41
  • 7Innominato P F,L6vi F A,Bjarnason G A.Chronotherapy and the molecular clock:clinical implications in oncology[J].Adv Drug Deliv Rev, 2010,62(9-10) :979-1001.
  • 8L6vi F,Okyar A,Dulong S,et al.Circadian timing in cancer treat- ments[J].Annu Rev Pharmacol Toxicol, 2010,50: 377-421.
  • 9L6vi F.Chronotherapeutics : the relevance of timing in cancer thera- py[J].Cancer Causes C ontrol, 2006,17 ( 4 ) : 611-621.

二级参考文献1

  • 1童建,冯致英.时间毒理学[J]国外医学(卫生学分册),1987(04).

共引文献40

同被引文献18

  • 1Lihong H, Linlin G, Yiping G, et al. Proteomics approaches for identification of tumor relevant protein targets in pulmonary squamous cell carcinomaby 2D-DIGE-MS[J]. PLoS One, 2014, 9(4): e95121.
  • 2Gong F, Peng XI, Luo C, et al. Cathepsin B as a potential prognostic and therapeutic marker for human lung squamous cell carcinoma[J]. Mol Cancer, 2013,12(1): 125.
  • 3Wang KI, Ling T, Wu H, et al. Screening of candidate tumor-suppressor genes in 3p21.3 and investigation of the methylation of gene promoters in oral squamous cell carcinoma[J]. Oncol Rep, 2013, 29(3): 1175-1182.
  • 4Tan J, Cang S, Ma Y, et al. Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents[J]. J Hematol Oncoi,2010,2(4):3-5.
  • 5Zaidi MI, Mallick A2. A study on assessment of mast cells in oral squamous cell carcinoma[J]. Ann Med Health Res, 2014, 4(3): 457-4 60.
  • 6Rivera CI, Venegas B2. Histological and molecular aspects of oral squamous cell carcinoma (Review)[J]. Oncoll Lett, 2014, 8(1): 7-11.
  • 7Pathak J, Swain N, Patel S, et al. Histopathological variants of oral squamous cell carcinoma-institutional case reports[J]. J Oral Maxillofac Pathol, 2014,18(1): 143-145.
  • 8Stockinger DEI, Fong DL2, Vogel KW2, et al. Oral Squamous Cell Carcinoma in a Pigtailed Macaque (Macaca nemestrina)[J]. Comp Med, 2014, 64(3): 234-239.
  • 9Nafarzadeh SI, Jafari S2, Bijani A3. Assessment of bax and bcl-2 immunoexpression in patients with oral lichen planus and oral squamous cell carcinoma[J]. Int J Mol Cell Med, 2013, 2(3): 136-142.
  • 10Prakash PI, Khandare M2, Kumar M3, et al. Immunohistochemical Detection of pl6 (INK4a) in Leukoplakia and Oral Squamous Cell Carcinoma[J]. J Clin Diagn Res, 2013, 7(12): 2793-2795.

引证文献1

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