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p27^(kip1)和p57^(kip2)在宫颈癌组织中的表达及其预后意义 被引量:1

Expressions of p27^(kip1) and p57^(kip2) in human cervix carcinoma and their prognostic significance.
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摘要 目的:探讨细胞周期调控抑制因子p27^(kip1)和p57^(kip2)在宫颈癌发生发展中的作用及预后意义。方法:采用免疫组化二步法检测p27^(kip1)和p57^(kip2)在48例宫颈癌(宫颈癌组)、13例宫颈上皮内瘤变(CIN组)和15例正常宫颈组织(正常组)中的表达。结果:p27^(kip1)和p57^(kip2)在宫颈癌组中的阳性表达率分别为25·00%和20·83%,显著低于正常组和CIN组(P<0·01,P<0·01),而后两组比较差异无统计学意义(P>0·05)。p27^(kip1)表达与宫颈癌病理分化程度显著相关(P<0·01);p57^(kip2)表达与宫颈癌病理分化程度及肿瘤大小有关(P<0·05,P<0·05);两者均与临床分期、组织学类型及淋巴结转移无关(均P>0·05)。p27^(kip1)与p57^(kip2)表达呈极显著正相关(r=0·621,P<0·01)。Kaplan-Meier单因素分析宫颈癌患者生存时间与p27^(kip1)及p57^(kip2)阳性表达有关(P<0·05,P<0·01)。结论:p27^(kip1)和p57kip2的低表达或缺失可能在宫颈癌发生发展中起重要作用,可能与预后不良有关。 Objective: To investigate the roles of the inhibitory factors of cell cycle regulation p27^kip1 and p57^kip2 in the development and advancement of the human cervix carcinoma and their clinicopathological and prognostic significance. Methods :The expressions of p27^kip1 and p57^kip2 in tumor tissues of 48 patients with cervix carcinoma and 13cases with cervical intraepithelial neoplasia(CIN) and 15 cases with normal cervical epithelium were detected by PolyHRP immunohistochemical technique. Results: p27^kip1 and p57^kip2 positive-expression rate in tumor tissues of cervix carcinoma was 25.00% and 20. 83% respectively, which were lower than those in CIN and normal cervical epithelial tissues (P 〈 0. 01, P 〈 0.01 ), and there was no significant difference in p27^kip1 and p57^kip2 staining between normal cervical epithelium and CIN groups(P 〉 0. 05 ). p27^kip1 positive-expression correlated significantly with tumor cell differenti- ation(P 〈0. 01 ). p57^kip2 positive-expression correlated significantly with tumor cell differentiation and lesion size ( P 〈 0. 05, P 〈 0. 05 ). p27^kip1 positive-expression correlated significantly with p57^kip2 positive-expression ( r = 0. 621, P 〈 0. 01 ). Kaplan-Meier estimation indicated that survival might be related to p27k^kip1 and p57^kip2 ( P 〈 0. 05, P 〈 0. 01 ) . Conclusion : The decreased expression or loss of p27^kip1 and p57^kip2 may play an important role in the development and progression of the cervical carcinoma, which is associated with poor prognosis.
出处 《现代妇产科进展》 CSCD 北大核心 2006年第1期32-35,共4页 Progress in Obstetrics and Gynecology
关键词 宫颈肿瘤 宫颈上皮内瘤变 P27^KIP1 P57^KIP2 免疫组织化学 Cervix neoplasms Cervicalintraepithelial neoplasia p27^kip1 p57^kip2 Immunohistochemistry
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参考文献14

  • 1Tak Hong Cheung,Keith Wing Kit Lo,May Mei Yung Yu,et al.Aberrant expression of p21^WAF1/CIP1 and p27^kip1 in cervical carcinoma[J].Cancer Lett,2001,172:93-98. 被引量:1
  • 2Shiozawa T,Shiohara S,Kanai M,et al.Expression of the cell cycle regulator p27(kip1)in normal squamous epithelium,cervical intraepithelial neoplasia,and invasive squamous cell carcinoma of the uterine cervix[J].Cancer,2001,92:3005-3011. 被引量:1
  • 3Reid LH,Crider-miller SJ,West A,et al.Genome organization of the human p57^kip2 gene and its analysis in the G401 Wilms tumor assay[J].Cancer Res,1996,56:1214-1218. 被引量:1
  • 4Tsihlias J,Kapusta L,Slingerland J.The prognostic significance of altered cyclin-dependent kinase inhibitors in human cancer[J].Annu Rev Med,1999,50:401-423. 被引量:1
  • 5Kawamata N,Morosetti R,Miller CW,et al.Molecular analysis of the cyclin-dependent kinase inhibitor gene p27^kip1 in human malignancies[J].Cancer Res,1995,55:2266-2269. 被引量:1
  • 6Lai S,Goepfert H,Gillenwater AM,et al.Loss of imprinting and genetic alterations of the cyclin-dependent kinase inhibitor p57kip2 gene in head and neck squamous cell carcinoma[J].Clin Cancer Res,2000,6:3172-3176. 被引量:1
  • 7Goff BA,Sallin J,Garcia R,et al.Evaluation of P27 in preinvasive and invasive malignancies of the cervix[J].Gynecol Oncol,2003,88:40-44. 被引量:1
  • 8Nakai S,Masaki T,Shirator Y,et al.Expression of p57^kip2 in hepatocellular carcinoma:relationship between tumor differentiation and patient survival[J].Int J Oncol,2002,20:769-775. 被引量:1
  • 9Sgambato A,Zannoni GF,Faraglia B,et al.Decreased expression of the CDK inhibitor p27^kip1 and increased oxidative DNA damage in the multistep process of cervical carcinogenesis[J].Gynecol Oncol,2004,92:776-83. 被引量:1
  • 10Farley J,Gray K,Prentice M,et al.Endocenical cancer is associated with an increase in the ligands and receptors for transforing growth factor-beta and a contrasting decrease in P27[J].Gynecol Oncol,2000,78:113-122. 被引量:1

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  • 1周正平,王进京,郑洪,苏俊,肖庆邦.乳腺浸润性导管癌中cyclinD_1、p57^(KIP2)的表达及意义[J].肿瘤防治研究,2005,32(8):476-478. 被引量:6
  • 2张素丽,郑红兵.cyclinE、CDK2在子宫平滑肌肿瘤中的表达[J].肿瘤防治研究,2006,33(7):531-532. 被引量:1
  • 3Mo L, Zheng X, Huang HY, et al. Hyperactivation of Haras oncogene, but not Ink 4a/Arf deficiency, triggers bladder tumorigenesis[J]. J Clin Invest, 2007,117(2): 314. 被引量:1
  • 4Okazaki K, Takada S. Dynamic energy landscape view of coupled binding and protein conformational change: inducedfit versus population shift mechanisms[J].Proc Natl Acad Sci USA, 2008,105(32): 11182- 11187. 被引量:1
  • 5Bahar I, Chennubhotla C, Tobi D. Intrinsic dynamics of enzymes in the unbound state and relation to allosteric regulation[J]. Curropin Struct Biol,2007, 17(6):633-640. 被引量:1
  • 6Lange OF, Lakomek NA, Far e C, et al. Recognition dynamics up to microsconds revealed from an RDC-derived ubiquitin ensemble in solution[J].Science,2008,320(5882):1471-1475. 被引量:1
  • 7Ivetac A, McCammon JA. Elucidating t he inhibition mechanism of HIV21 nonnucleoside reverset ranscriptase inhibitors through multicopy molecular dynamics simulations[J].J Mol Biol, 2009,388(3): 644-658. 被引量:1
  • 8Sullivan SM, Holyoak T. Enzymes with lid-gated active sites must operate by an induced fit mechanism instead of conformational selection[J].Proc Natl Acad Sci USA,2008,105(37): 13829-13834. 被引量:1
  • 9Yang LW, Eyal E, Bahar I, et al. Principal component analysis of native ensembles of biomole cular structures(PeA- NEST): insights into functional dynamics[J].Bioinformatics,2009, 25(5):606-614. 被引量:1
  • 10Yang L, Song G, Carriquiry A, et al. Close correspondence between the motions from principal component analysis of multiple HIV21 protease structures and elastic network modes[J]. Structure, 2008,16(2): 321-330. 被引量:1

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