期刊文献+

Endostar联合放疗对Lewis肺癌小鼠生长及AQP1、HIF-1α mRNA表达的影响 被引量:4

Effect of Endostar Combined with Radiotherapy on the Expression of Aquaporin 1 and Hypoxia-Inducible Factor-1 Alpha mRNA and Growth of Mice with Lewis Lung Cancer
原文传递
导出
摘要 目的:探讨Endostar联合放射治疗对Lewis肺癌小鼠移植瘤生长及介导氧跨膜转运的水通道蛋白1(AQP1)及乏氧诱导因子-1α(HIF-1α)mRNA表达的影响。方法:将32只Lewis肺癌移植瘤小鼠随机分为4组:空白对照组、单用Endostar组(ES组)、单用放疗组(RT组)、Endostar联合放疗组(ES+RT组),对各组肿瘤组织中AQP1及HIF-1αmRNA的表达情况进行检测。结果:AQP1mRNA的表达:与对照组相比,ES组变化无统计学差异(P>0.05)、RT组降低(P<0.05)、ES+RT组升高(P<0.05);HIF-1αmRNA的表达:与对照组相比,ES组变化无统计学差异(P>0.05)、RT组与ES+RT组均降低(P<0.05)。Pearson分析AQP1mRNA与HIF-1αmRNA的表达呈负相关(r=-0.58,P<0.01)。结论:Endostar联合放疗可能通过上调AQP1mRNA表达,增加细胞摄氧量,抑制HIF-1αmRNA表达,而增强射线对肿瘤细胞的杀伤作用。 Objective: To explore the effect of Endostar combined with radiotherapy on the mRNA expression of aquaporin 1 (AQP1) which mediated transmembrane transport of oxygen and hypoxia-inducible factor-1α (HIF-1α) in tumor-bearing mice with Lewis lung cancer. Methods: Thirty-two tumor-bearing mice were randomly divided into four groups: control group, Endostar group, radiation therapy group, and Endostar combined with radiotherapy group. After treatment, the tumor growth curve was calculated, and the real time PCR was used to detect the different expression of AQP1 and HIF-1α mRNA in each group. Results: Compared with that in control group, the expression of AQP1 mRNA had no changes in Endostar group (P0.05), decreased in radiotherapy group (P0.05), and increased in Endostar combined with radiotherapy (P0.05). Compared with control group, the expression of HIF-1α mRNA had no changes in Endostar group (P0.05), and was lower both in radiotherapy group and Endostar combined with radiotherapy group (both P0.05). There existed negative correlation between the expression of AQP1 and HIF-1α mRNA (r=-0.58,P0.01). Conclusion: Endostar combined with radiotherapy may enhance the tumor killing effect of radiation therapy through increasing AQP1 mRNA expression and inhibiting the HIF-1α mRNA expression, which enhances the oxygen uptake of cells, thereby increases the killing effect of radiation on tumor cells.
出处 《武汉大学学报(医学版)》 CAS 北大核心 2011年第1期44-48,共5页 Medical Journal of Wuhan University
基金 国家自然科学基金资助项目(编号:30970860)
关键词 ENDOSTAR 放射治疗 水通道蛋白1 乏氧诱导因子-1Α Endostar Radiotherapy Aquaporin 1 Hypoxia-Induced Factor-1α
  • 相关文献

参考文献15

  • 1Huang X, Wong MK, Zhao Q, et al. Soluble recombi- nant endostatin purified from Escherichia- coli: antian- giogenic activity and antitumor effect [J]. Cancer Res, 2001, 61(2) :478-481.
  • 2Li B, Wu XY, Zhou H, et al. Acid-induced unfolding mechanism of recombinant human endostatin[J]. Bio- chemistry,2004,43(9) :2 550-2 557.
  • 3Folkman J. Tumor angiogenesis: therapeutic implica- tions[J]. N Engl J Med,1971,285(21): 1 182-1 186.
  • 4Schmidt C. Why do tumors become resistant to antian- giogenesis drugs?[J]. J Natl Cancer Inst, 2009,101 (22):1 530-1 532.
  • 5Azam F, Mehta S, Harris AL. Mechanisms of resist- ance to antiangiogenesis therapy [J]. Eur J Cancer, 2010, Mar 16. [Epub ahead of print].
  • 6O'Reilly MS, Boehm T, Shing Y, et al. Endostatin; an endogenous inhibitor of angiogenesis and tumor growth[J]. Cell, 1997, 88(2): 277-285.
  • 7隋刚,徐志飞,孙耀昌,刘永靖,乌立晖,秦雄.腺病毒介导的内皮抑素基因治疗小鼠肺癌[J].中华肿瘤杂志,2008,30(2):93-96. 被引量:8
  • 8Jain RK. Normalization of tumor vasculature: An emerging concept in antiangiogenic therapy[J]. Sci- ence,2005,307(5 706) :58-62.
  • 9Wachsberger P, Burd R, Dicker AP. Tumor response to ionizing radiation combined with antiangiogenesis or vascular targeting agents: exploring mechanisms of in- teraction[J]. Clin Cancer Res, 2003,9(6): 1 957- 1 971.
  • 10Echevarria M, Munoz-Cabello AM, Sanchez-Silva R,et al. Development of cytosolic hypoxia and hypoxia-in- ducible factor stabilization are facilitated by aquaporin-1 expression[J]. J Biol Chem, 2007, 282(41) : 30 207- 30 215.

二级参考文献30

共引文献35

同被引文献33

  • 1吴欣爱,孙燕,樊青霞,王留兴,王瑞林.乏氧诱导因子1α在食管鳞癌中的表达及其与化疗疗效的关系[J].中华医学杂志,2007,87(25):1783-1785. 被引量:10
  • 2Liu L,Zhang JZ,Li CH,et al. Study of the impact of CT/CT image fusion radiotherapy on V20 and radiation pneumonitis of non- small cell lung cancer[J]. Chinese- German Jour- nal of Chnical Oncology ,2012,11 (2) :72 -75.
  • 3Folkman J. Tumor angiogenesis: therapeutic implication [J]. N Engl J Med,1971,285(20) :1182 - 1186.
  • 4Samaranayake H, Miatta AM, Pikkarainen J, et al. Future prospects and challenges of antiangiogenic cancer gene ther- apy[ J]. Hum Gene Thor,2010,21 (4) :381 - 396.
  • 5Azam F, Mehta S, Harris AL. Mechanisms of resistance to antiangiogenesis therapy [ J ]. Eur J Cancer, 2010,46 ( 8 ) : 1323 - 1332.
  • 6Jain RK. Normalization of tumor vasculature:an emerging concept in antiangiogenic therapy [ J ]. Science, 2005,307 (5706) :58 -62.
  • 7Kaluzova M, Pastorekova S, Svastova E, et al. Characteriza- tion of the MN/CA9 proximal region : a role for SP and AP1 factors [ J]. Biochem J,2001,359 :669 - 677.
  • 8Goel S, Fukumura D, Jain RK. Normalization of the tumor vasculature through oncogenic inhibition:an emerging paradigm in tumor biology [J]. Proc Natl Acad Sci U S A,2012,109(20) :E1214.
  • 9Rozman A, Silar M, Kosnik M. Angiogenin and vascular endothelial growth factor expression in lungs of lung cancer patients [ J ]. Radiol 0ncol,2012,46(4) :354-359.
  • 10张彦彦,戈伟,赵娟,赵振宇,李长虎.内皮抑素联合放射治疗对A549细胞生长及HIF-1表达的影响[J].中国肺癌杂志,2009,12(1):33-37. 被引量:9

引证文献4

二级引证文献13

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