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结直肠癌组织HDAC1 mRNA表达临床意义的探讨 被引量:2

Expression of HDAC1 mRNA in colorectal cancer tissues
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摘要 目的:探讨HDAC1mRNA在结直肠癌组织中的表达并分析其临床意义。方法:RT-PCR检测50例结直肠癌组织、50例癌旁组织、20例正常结直肠组织和20例腺瘤组织中HDAC1mRNA表达情况,统计学分析HDAC1mRNA相对表达量与患者临床病理特征关系。结果:癌组织HDAC1mRNA相对表达量(0.608±0.032)明显高于癌旁组织(0.496±0.026),腺瘤组织HDAC1mRNA相对表达量(0.495±0.052)明显高于正常组织(0.388±0.050);癌组织中HDAC1mRNA相对表达量与患者的性别(t=0.264,P=0.793)、年龄(t=0.116,P=0.908)和肿瘤大小(t=0.621,P=0.537)无关,而与组织Duke分期(t=3.395,P=0.001)、组织学分型(t=2.070,P=0.043)和淋巴结转移(t=2.162,P=0.036)相关。Duke C、D期HDAC1mRNA相对表达量明显高于Duke A、B期,高、中分化结直肠癌组织HDAC1mRNA相对表达量明显低于低、未分化组织,淋巴结转移患者HDAC1mRNA相对表达量增高。CK20(t=2.389,P=0.021)和Ki-67(t=2.117,P=0.039)高表达患者HDAC1mRNA相对表达量明显增高。结论:HDAC1mRNA高表达与结直肠癌患者临床病理学特征相关。RT-PCR检测HDAC1mRNA在结直肠癌组织中的表达,可能成为一种新的结直肠癌特异性诊断标志。 OBJECTIVE:To study the expression of HDAC1 mRNA in colorectal cancer and analysis its correlation with clinicopathological features. METHODS: The expression of HDAC] mRNA was detected in 50 cases of colorectal cancer and their corresponding adjacent tissues,20 cases of normal tissues and 20 cases of adenoma tissues by R'F-PCR. The correlation with clinicopathological features was analized by Chi-square test. RESULTS: HDAC1 mRNA expresskm was higher in colorectal cancer(0. 608±0. 032) than that in cancer corresponding adjacent tissues(0. 496±0. 026),and ad enoma tissues(0.495_+_0.052) had a higher expression of HDAC1 mRNA than that of normal tissues(0. 388±0. 050). The expression of HDAC1 mRNA in Duke A and B stages(t=3. 395,P=0. 001) was significantly lower than that in Duke and D stages. The expression of HDAC1 mRNA in lowly- and non-differentiated adenoma(t = 2. 070, P〈 0. 043) was significantly higher than that in the highly and moderately-differentiated adenoma. In addition,the expresskm of HDAC1 mRNA was correlated with lymph node metastasis(t=2. 162,P=0. 036) ,but not with age(t=0.116,P=0. 908) ,sex(t= 0.26,1,P=0.793) and tumor sizes(t=0.621,P--0.537) of patients. The expression of HDAC1 mRNA has a positive correlation with Ki-67(t 2. 117,P=0. 039) and CK20(t=2. 389,P=0.021) expression in cancer tissue. CONCLU- SIONS: HDAC1 mRNA overexpression in colorectal cancer indicates an unfavorable clinicopathological feature. Detection of HDAC1 mRNA may be a new diagnostic method in patients with colorectal cancer .
出处 《中华肿瘤防治杂志》 CAS 北大核心 2013年第4期288-291,共4页 Chinese Journal of Cancer Prevention and Treatment
关键词 结直肠肿瘤 组蛋白去乙酰化酶 逆转录聚合酶链反应 病理学 临床 colorectal neoplasms HDAC1 reverse transcriptase polymerase chain reaction pathology,clinical
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  • 1Segre CV,Chiocca S. Regulating the regulators: the post-translational code of class I HDAC1 and HDAC2[J]. J Biorned Biotechnol,2011,2011: 690848.
  • 2Sudo T,Mimori K,Nishida N,et al. Histone deacetylase 1 expression in gastric cancer[J]. Oncol Rep,2011,26(4) : 777-782.
  • 3Senese S,Zaragoza K,Minardi S, et al. Role for histone deacety-lase 1 in human tumor cell proliferation[J]. Mol Cell Biol, 2007, 27(13): 4784-4795.
  • 4Liu PY, Hsieh TY, Liu ST. Zacl, an Spl-like protein, regulates human p21 (WAF1/Cipl) gene expression in HeLa cells [J].Exp Cell Res,2011,317(20):2925-2937.
  • 5Dangond F, Henriksson M, Zardo G, et al. Differential expression of class I HDACs:roles of cell density and cell cycle[J]. Int J Oncol,2001,19(4):773-777.
  • 6Silvia S, Katrin Z, Simone M, et al. Role for histone deacetylase 1 in human tumor cell proliferation [J]. Mol Cell Biol, 2007, 27(13) :4784-4795.
  • 7Lagger G, O'CarroH D, Rembold M, et al. Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression[J]. EMBO J, 2002,21(11) : 2672-2681.
  • 8张孟贤,韩娜,于世英.RNA干扰沉默HDAC1基因对大肠癌细胞增殖和凋亡的影响[J].世界华人消化杂志,2008,16(11):1173-1178. 被引量:5
  • 9Zhang CZ, Chen GG, Merchant JL, et al. Interaction between ZBP-89 and p53 mutants and its contribution to effects of HDACi on hepatocellular carcinoma[J]. Cell Cycle,2012,11(2):322-334.
  • 10Khabele D,Son DS,Parl AK,et al. Drug-induced inactivation or gene silencing of class I histone deacetylases suppresses ovarian cancer cell growth:implications for therapy[J]. Cancer Biol Ther, 2007,6(5) : 795-801.

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