期刊文献+

肺非小细胞癌患者中p53、bax的差异表达

Study on transcription status of p53、bax in lung cancers.
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摘要 目的探讨p53、bax抑癌基因在肺非小细胞癌组织及癌旁组织中的差异表达。方法以凝胶上rRNA条带的亮度为依据对后续分析用的起始RNA浓度进行调整;以组成型表达的β-actin基因为外对照,对两类组织来源的起始RNA量进行监测;基因克隆及序列分析来验证所用引物的可靠性;随后采用逆转录-聚合酶链式反应(RT-PCR)的方法对各基因在两类组织中的表达谱进行对比分析,并以Northern杂交加以验证。结果在两类组织来源的起始RNA量基本一致的前提下,p53、bax 2个抑癌基因在成对组织中的表达谱存在明显差异。bax在肺癌组织及癌旁组织中均有表达;p53基因在肺癌组织中的表达量较高,且p53的带型与在癌旁组织中表现也明显不同。结论肺癌组织及癌旁组织中存在bax促凋亡基因的转录;p53基因在肺癌组织出现异常转录。 Objective To study the different expression of anti oncogenes p53, bax in lung cancer tissues and its paracancer tissues from different patients. Methods The start concentration of all RNAs were adjusted for the consequent use according to the brightness of rRNA bands displayed on agarose gel. Constitutive expression of B - actin gene was used as external control to monitor the beginning amounts of RNAs from two kinds of tissues. The reliability of all primers used for RT - PCR was confirmed by gene cloning and sequencing. The expression profiles of two genes were then analyzed in tissue parallel by applying RT - PCR. The results were further confirmed by Northern Blot. Results By using similar amount of initial RNAs, two cantioneo genes were differently expressed in the two kinds of tissues, bax were expressed both in lung cancer tissues and paracancer tissues, while p53 exhibited higher expression in lung cancer tissues than in paracancer tissues. Furthermore, the band profile of p53 in lung cancer tissue was sharply different from that in the paracancer tissues. Conclusion The proapoptosis gene bax was unexpectedly tranScribed in lung cancer tissues, suggesting the less effect on the cancer cure by simple apoptosis - promoting method. The abnormal transcription of p53 gene in lung cancer tissue may play an important role on cancer development.
出处 《现代肿瘤医学》 CAS 2005年第6期724-727,共4页 Journal of Modern Oncology
基金 军队医药卫生十五科研基金资助课题(编号01MA101)
关键词 肺肿瘤 P53 BAX lung neoplasm p53 bax
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参考文献13

  • 1Oltvai ZN, Milliman CL, Korsmeyer SJ. Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death[J]. Cell, 1993, 74(4):609~619.
  • 2张莉,李瑞芬.p53、p16、Bcl-2基因及产物在原发性肺癌中的表达及其临床病理意义[J].新疆医科大学学报,2002,25(1):57-60. 被引量:4
  • 3Yoon JH, Lee CS, Pfeifer GP. Simulated sunlight and benzo[a]pyrene diol epoxide induced mutagenesis in the human p53 gene evaluated by the yeast functional assay: lack of correspondence to tumor mutation spectra[J]. Carcinogenesis, 2003, 24(1):113~119.
  • 4Conway K, Edmiston SN, Cui L, et al. Prevalence and spectrum of p53 mutations associated with smoking in breast cancer[J]. Cancer Res, 2002, 62(7):1987~1995.
  • 5陶爱林,何韶衡.豚草花粉泛过敏原同源基因克隆与序列分析[J].中华微生物学和免疫学杂志,2004,24(3):169-173. 被引量:10
  • 6顾其华,陈琼,张贻秋,李叶青,叶爱慧.肺鳞癌、肺腺癌Ki-ras和p53基因序列分析[J].中国现代医学杂志,2003,13(1):24-27. 被引量:6
  • 7Dumont P, Leu JI, Della Pietra AC, et al. The codon 72 polymorphic variants of p53 have markedly different apoptotic potential[J]. Nat Genet, 2003, 33(3):357~365.
  • 8Olivier M, Eeles R, Hollstein M, et al. The IARC TP53 database: new online mutation analysis and recommendations to users[J]. Hum Mutat, 2002, 19(6):607~614 .
  • 9Pim D, Banks L. p53 polymorphic variants at codon 72 exert different effects on cell cycle progression[J]. Int J Cancer, 2004, 108(2):196~199.
  • 10Massion PP, Taflan PM, Jamshedur Rahman SM, et al. Significance of p53 amplification and overexpression in lung cancer development and prognosis[J]. Cancer Res, 2003, 63(21):7113~7121.

二级参考文献26

  • 1喻伦银,王虹,毕勇毅,刘铭球,邹祖玉,张正彬.p53基因突变与肺癌发生的早期遗传学损害[J].中华医学遗传学杂志,1996,13(3):161-163. 被引量:6
  • 2Villalba M, Batanero E, Monsalve RI, et al. Cloning and expression of Ole e I, the major allergen from olive tree pollen. Polymorphism analysis and tissue specificity. J Biol Chem, 1994, 269(21): 15217-15222.
  • 3Krebitz M, Wiedermann U, Essl D, et al. Rapid production of the major birch pollen allergen Bet v 1 in Nicotiana benthamiana plants and its immunological in vitro and in vivo characterization. FASEB J, 2000, 14: 1279-1288.
  • 4Laffer S, Duchene M, Reimitzer I, et al. Common IgE-epitopes of recombinant Phl p I, the major timothy grass pollen allergen and natural group I grass pollen isoallergens. Mol Immunol, 1996, 33(4-5): 417-426.
  • 5Tamura Y, Kawaguchi J, Serizawa N, et al. Analysis of sequential immunoglobulin E-binding epitoped of Japanese cedar pollen allergen (Cry j 2) in humans, monkeys and mice. Clin Exp Allergy, 2003, 33: 211-217.
  • 6Check E. The virtue of tolerance. Nature, 2002, 418: 364-367.
  • 7Singh MB, Bhalla PL. Hypoallergenic derivatives of major grass pollen allergens for allergy vaccination. Immunol Cell Biol, 2003, 81: 86-91.
  • 8Scholl I, Wiedermann U, Forster-Waldl E, et al. Phage-displayed Bet mim 1, a mimotope of the major birch pollen allergen Bet v 1, induces B cell responses to the natural antigen using bystander T cell help. Clin Exp Allergy, 2002, 32(11): 1583-1588.
  • 9Yu CJ, Lin YF, Chiang BL, et al. Proteomics and immunological analysis of a novel shrimp allergen, Pen m 2. J Immunol, 2003, 170: 445-453.
  • 10Hemmer W, Focke M, Wantke F, et al. Ash (Fraxinus excelsior)-pollen allergy in central Europe: specific role of pollen panallergens and the major allergen of ash pollen, Fra e 1. Allergy, 2000, 55: 923-930.

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