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Bmi-1在大肠癌组织中的表达及意义 被引量:4

Expression of Bmi-1 in colorectal carcinoma and its clinical significance
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摘要 目的:探讨Bmi-1基因的表达与大肠癌病理学特征的相关性及其在大肠癌发生发展中可能的作用机制。方法:收集我院50例大肠癌组织标本,50例正常组织作为对照。利用实时荧光定量PCR(FQ-PCR)法检测标本中Bmi-1 mRNA的表达,同时利用免疫组化法检测Bmi-1和P16蛋白的表达,并结合大肠癌的临床病理学资料,分析Bmi-1基因的表达与大肠癌临床病理特征之间的关系。结果:Bmi-1mRNA及蛋白在大肠癌组织中的表达明显高于正常组织(P<0.05),免疫组化提示大肠癌组织高表达Bmi-1蛋白的同时伴有P16蛋白的低表达(P<0.05)。Bmi-1的表达与肿瘤体积大小、Dukes分期、淋巴结转移、远处转移和P16蛋白的表达水平密切相关(P<0.05),而与患者性别、年龄、血清CEA、血清CA19-9、P53等无相关性(P>0.05)。结论:Bmi-1癌基因可能通过抑制P16蛋白的表达而促进大肠癌的发生发展,检测其表达可判断大肠癌的预后。 Objective To investigate the relationship between Bmi-1 expression and the pathologic features of colorectal carcinoma and the possible role of the expression in the genesis and development of the malignancy. Methods We collected 50 samples of colorectal cancer tissue and 50 samples of normal controlled tissue to detect both Bmi-lmRNA expression by real-time, fluorescence-based quantitative PCR and the expressions of Bmi-1 and p16 protein using immunohistochemistry. Then we analyzed the association of Bmi-1 expression with the pathologic features of the tumor. Results Significantly higher expression levels of Bmi-1 gene and protein and a lower expression of pI6 protein were detected in the cancer tissue than in the normal tissue (P 〈 0.05 for both comparisons). Bmi-1 expression was closely associated with tumor size, Dukes' stages, lymph node involvement, distant metastasis, and P16 expression (P 〈 0.05) ; but not associated with sex, age, serum CEA, CA19-9 level, or P53 overexpression (P 〉 0.05). Conclusions Bmi-1 gene may accelerate the genesis and growth of eolorectal carcinoma by suppressing the expression of P16 protein. Determination of Bmi-1 expression can predict prognosis.
出处 《实用医学杂志》 CAS 北大核心 2009年第21期3589-3591,共3页 The Journal of Practical Medicine
关键词 肠肿瘤 BMI-1 P16 FQ—PCR 免疫组化 Intestinal neoplasms Bmi-1 P16 FQ-PCR Immunohistochemistry
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参考文献10

  • 1黄开红,刘建化,李学先,宋立兵,曾木圣.Bmi-1基因过度表达与胃癌分化、转移及预后的关系[J].南方医科大学学报,2007,27(7):973-975. 被引量:32
  • 2Vonlanthen S, Heighway, Altermatt H J, et al. The Bmi-1 oncoprotein is differentially expressed in non-small cell lung cancer and correlates with INK4A-ARF locus expression [J]. BJC, 2001, 84(10) : 1372-1376.
  • 3Song L B, Zeng M S, Liao W T, et al. Bmi-1 is a novel molecular marker of nasopharyngeal carcinoma progression and immortalizes primary human nasopharyngeal epithelial cells [J]. Cancer Res, 2006, 66(12) : 6225-6232.
  • 4冯艳,宋立兵,郭宝红,廖雯婷,李满枝,刘万里,曾木圣,张玲.Bmi-1在乳腺癌组织中的表达及意义[J].癌症,2007,26(2):154-157. 被引量:67
  • 5Kamb A, Gruis N A, Weavev-Feldhaus J, et al. A cell cycle regulator potentially involved in genesis of many tumor types [J]. Science. 1994, 264(5157): 436-440.
  • 6Shapiro G I, Edwards C D, Ewen M E, et al. p16INK4A participates in a GI arrest checkpoint in response to DNA damage [J]. Mol Cell Biod, 1998, 18(1):378-387.
  • 7Wang H, Pan K, Zhang H K, et al. Increased poly-comb-group oncongene Bmi-1 expression correlates with poor prognosis in hepatocellular carcinoma [J]. Cancer Res Clin Oncol, 2008, 134(5): 535-541.
  • 8Herman J G, Abouezzi Z, Borgen P I, et al. Inactivation of the CDKN2/P16/MTS1 gene is frequently associated with abetrant DNA methytation all common human cancers [ J ]. Cancers, 1995,55 ( 1 8) : 4525-4530.
  • 9谢明,李建平.抑癌基因p16突变与乳腺癌的相关研究[J].中国现代医药杂志,2007,9(4):5-7. 被引量:8
  • 10Jares P, Fernanclez P I, Campo E, et al. PRAD-1/cycleD1 gene amplification correlates with messenger RNA over expression and tumor progression in human laryngeal carcinomas [J]. Cancers, 1994,549(17) :4813-4817.

二级参考文献32

  • 1刘卫红,孟秀香,刘丹丹,单路娟,赵心宇.反义Bmi-1对Jurkat细胞的抑制作用[J].中华血液学杂志,2005,26(9):554-556. 被引量:19
  • 2龚辉,张义成,刘文励.Bmi-1基因调控造血干细胞自我更新的研究进展[J].中国实验血液学杂志,2006,14(2):413-415. 被引量:11
  • 3[2]Uchida F,kinoshiya F,Saita H,et al.CDKN2(MTA1/p16INK4A)gene alterations in hematological malignancies[J].Leak-Lym phoma,1997,24(5-6):449-461
  • 4[3]Luca M,Xie S,Gutran M,et al.Abnormalities in the CDKN2(p16INK4/MTS-1) gene in human melanoma cells:relevance to tumor growth and metastasis.Ontogeny,1995,11:1399-1402
  • 5[4]Heman JG,Merlo A,Mao l,et al.Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA ethylating in all common human cancers.Cancer Res,1995,55:4525-4530
  • 6[5]Okamoto A,Demetrick DJ,Spillart EA,et al.Mutations and altered expression of p16 (INK4) in human cancer[J].Prenatal Aced Sick USA,1994,19:11045-11049
  • 7[8]Chen WM,Zhu JZ,Liu LZ.et al,methylamine of p16 gene in hematological malignancies.Chin Med[J],1998,111:1028-1030
  • 8Van L M, Verbeek S, Scheijen B, et al. Identification of cooperating oncogenes in E~-myc transgenic mice by provirus tagging [J]. Cell, 1991,65(5):735-752.
  • 9Haupt Y, Alexander W S, Barri G, et al. Novel zinc finger gene implicated as myc collaborator by retrovirally accelerated lymphomagenesis in Eμ-myctransgenic mice [J]. Cell, 1991,65 (5): 753-763.
  • 10Itahana K, Zou Y, Itahana Y, et al. Control of the replicative life span of human fibroblasts by p16 and the polycomb protein Bmi- 1 [J]. Mol Cell Biol, 2003,23 (1):389-401.

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