期刊文献+

宫颈癌hMSH2、突变型P53及PTEN蛋白的异常表达 被引量:2

Abnormal expressions of hMSH2,mutated P53 and PTEN proteins in cervical carcinoma
下载PDF
导出
摘要 [目的]探讨宫颈癌hMSH2、突变型P53及PTEN蛋白的异常表达在宫颈癌发病中的作用及临床意义。[方法]免疫组织化学SP法定位检测61例宫颈癌和19例慢性宫颈炎组织hMSH2、突变型P53及PTEN蛋白的表达情况。[结果]宫颈癌与慢性宫颈炎组,hMSH2蛋白阳性表达率分别为57.38%(35/61)和21.05%(4/19)(P<0.05);突变型P53蛋白阳性表达率分别为70.49%(43/61)和15.79%(3/19)(P<0.05);PTEN蛋白阳性表达率分别为59.02%(36/61)和26.32%(5/19)(P<0.05);三种蛋白共同表达率分别为29.51%(18/61)和5.26%(1/19)(P<0.05)。宫颈癌hMSH2蛋白表达阳性组与阴性组,突变型P53蛋白的阳性表达率分别为77.14%(27/35)、61.54%(16/26),差异无显著意义(P>0.05);PTEN蛋白的阳性表达率分别为62.86%(22/35)、53.85%(14/26),差异无显著意义(P>0.05)。宫颈癌突变型P53蛋白表达阳性组与阴性组,PTEN蛋白的阳性表达率分别为62.79%(27/43)、50.00%(9/18),差异无显著意义(P>0.05)。[结论]宫颈癌的发病过程中伴有hMSH2、突变型P53及PTEN蛋白表达上调,但三者高表达机制各自独立。3种蛋白联合检测有助于宫颈癌的预警和诊断。 [ Objective] To study the significance of abnormal expressions of DNA mismatch repair ( hMSH2), mutated P53 and PTEN proteins in cervical carcinogenesis. [ Method] Immunohistochemistry SP method was used to detect the expressions of hMSH2 , mutated P53 and PTEN proteins in 61 cases, cervical carcinomas and 19 cases chronic cervicitises. [ Results] In cervical carcinoma and chronic cervicitis groups, the protein expression rates of hMSH2 were 57.38% and 21.05% (P 〈 0.05); the rates of mutated P53 were 70.49% and 15.79% ( P 〈 0.05 ) ; the rates of PTEN were 59.02% and 26.32% ( P 〈 0.05) ; the rates of three proteins at the same case were 29.51% and 5.26% (P 〈 0.05 ). In cervical carcinoma with the hMSH2 expression and without, the protein expression rates of mutated P53 were 77.14% and 61.54% respectively ( P 〉 0.05 ) ; the rates of PTEN were 62.86% and 53.85% respectively ( P 〉 0.05 ). In cervical carcinoma with the Mutated P53 expression and without, the protein expression rates of PTEN were 62. 79% and 50.00% respectively ( P 〉 0.05 ). [ Conclusion ] Following the cervical carcinogenesis, the expressions of hMSH2, mutated P53 and PTEN proteins increase independently. It may be helpful for predicting and diagnosing cervical carcinoma to detecting expressions of three proteins at the same time
出处 《大连医科大学学报》 CAS 2007年第4期343-344,348,共3页 Journal of Dalian Medical University
关键词 宫颈癌 HMSH2 P53 PTEN 免疫组织化学 cervical carcinoma hMSH2 P53 PTEN immunohistochemistry
  • 相关文献

参考文献8

  • 1Peltomaki P.DNA mismatch repair and cancer[J].Mutat Res,2001,488 (1):77-85.
  • 2周琪,阎晓初.人类错配修复基因突变在大肠肿瘤发生中的作用研究新进展[J].重庆医学,2004,33(7):1044-1047. 被引量:4
  • 3刘飞飞,李梅,王朝晖,吕申.hMSH2蛋白和P53蛋白表达在胃癌发病中的意义[J].大连医科大学学报,2006,28(4):286-287. 被引量:2
  • 4Klingler H,Hemmerle C,Bannwart F,et al.ExPression of the hMSH6 mismatch -repair Protein in colon cancer and Hela cells[J].Swiss Med Wkly,2002,132 (5-6):57 -63.
  • 5郭丰,史锦云,胡玉芳.EB病毒感染与子宫颈癌[J].肿瘤防治研究,1998,25(2):81-82. 被引量:12
  • 6Vogelstein B,Kinzler KW.P53 function and dysfunction[J].Cell,1992,70(4):523 -526.
  • 7Gu J,Tamura M,Yamada KW.Tumor suPPressor PTEN inhibits integrin-and growth factor-mediated mitogen-activated Protein (MAP) kinase signaling Pathways[J].J Cell Biol,1998,143(5):1375 -1383.
  • 8Yaginuma Y,Yamashita T,Ishiya T,et al.Abnomal structure and exPression of PTEN/MMAC1 gene in human uterine cancers[J].Gynecol 0ncol,2000,76 (2):193-199.

二级参考文献28

  • 1张娜.肿瘤抑制基因P^(53)研究进展[J].中国中西医结合外科杂志,2004,10(4):337-339. 被引量:2
  • 2Riccardo D,Alessandra V,Claudio D,et al.High prevalence of activatied intraepithelial cytotoxic T lymphocytes and increased neoplastic cell apoptosis in colorectal carcinoma with microsatellite instability[J].Am J Pathol,1999,154:1805
  • 3Shigemasa K,Yokozaki H,Honda N,et al.Microsatellite instability and hMSH2 gene mutation in a triple cancer (colon cancer,endometrial cancer,ovarian cancer) patient in hereditary non-polyposis colorectal cancer (HNPCC) kindred[J].J Obstet Gynaecol Res,1999
  • 4Zhang H,Richards B,Wilson T,et al.Apoptosis induced by overexpression of hMSH2 or hMLH1[J].Cancer Res,1999,59(13): 3021
  • 5Jiricny,Nystrom-Lahti M.Mismatch repair defects in cancer[J].Curr Opin Genet,2000,10:157
  • 6Kohonen MR,Daniel JJ,Riele H,et al.Susceptibility of Msh2-deficient mice to inflammation-associated colorectal tumors[J].Cancer Res,2002,62(7):2092
  • 7Noffsinger AE,Belli JM,Fogt F,et al.A germline hMSH2 alteration is unrelated to colonic microsatellite instability in patients with ulcerative colitis[J].Hum Pathol,1999,30:8
  • 8Cawkwell L,Sutherland F,Murgatoryd H,et al.Defective hMSH2/hMLH1 protein expression in seen infrequently in ulcerative colitis associated colorectal cancers[J].Gut,2000,46:367
  • 9Toyota M,Lssa JP.CpG island methylator phenotypes in aging and cancer[J].Semin Cancer Biol,1999,9:349
  • 10Kuismanen SA,Holmberg MT,Salovaara R,et al.Epigenetic in phenotypes distinguish microsatellite stable and unstable colorectal cancer[J].Proc Natl Acad Ssi USA,1999,96:12661

共引文献15

同被引文献19

  • 1王雪梅,吕申,王朝辉,富晶,张朝,胡波.hMSH2和PTEN在肺腺癌中的表达及意义[J].大连医科大学学报,2005,27(3):174-175. 被引量:1
  • 2王花丽,吕申.PTEN和hMSH2蛋白的表达在胃癌发生中的作用[J].大连医科大学学报,2006,28(5):364-365. 被引量:1
  • 3周琦,叶学正,唐郢,黄海萍,张代奎.PTEN基因在宫颈癌中的表达及与预后的关系[J].肿瘤学杂志,2007,13(2):121-122. 被引量:11
  • 4张培荣,郑锦花,王艳萍,李曦红,富浩然,黄梅竹,戚基萍.Survivin和PTEN蛋白在宫颈鳞状细胞癌中的表达及临床意义[J].临床肿瘤学杂志,2007,12(4):271-275. 被引量:10
  • 5Lee JS, Choi YD, Lee JH, et al. Expression of PTEN in the progression of cervical neoplasia and its relation to tumor behavior and angiogenesis in invasive squanlous cell carcinoma[J].Surg Oncol,2006,93(3) :233-240.
  • 6Lynch HT, de-la Chaplle A. Genetic susceptibility to nonpolyposis colorectal cencer[ J]. J Med Genet, 1999,36( 11 ) : 801-818.
  • 7Fishel R, Lescoe MK, Rao MRS, et al. The human mutator gene homolog hMSH2 and its association with hereditary nonpolyposis colon cancer [J]. cell, 1993 75:1 027-1 036.
  • 8Chialina SG, Fomes C, Landi C, et al. Microsatellite instability analysis in hereditary non-polyosis colon cancer using the Bethesda consensus panel of microsatellite markers in the absence of proband normal tissue [ J ]. BMC Med Genet, 2006,7 : 5.
  • 9Kamory E, Kolaesck O, Otto S, et al. hMLHI and hMSH2 somatic inactivation mechanisms in sporadic colorectal cancer patients[J].Pathol Oncol Rcs, 2003,9(4) :236-241.
  • 10Srivastava T, Chattopadhyay P, Mahapatra AK, et al. Increased hMSH2 protein expression in glioblastoma multiforme[J].J Neurooncol, 2004,66( 1-2): 51-57.

引证文献2

二级引证文献6

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