期刊文献+

p57^(kip2)与cyclin D1在上皮性卵巢癌中的表达及临床意义 被引量:1

Expressions of p57^(kip2) and cyclin D1 Proteins in Epithelial Ovarian Carcinoma and Their Clinical Significance
下载PDF
导出
摘要 目的研究p57kip2与细胞周期素D1在上皮性卵巢癌中的表达与临床病理特征的关系,探讨其在上皮性卵巢癌发生发展过程中的作用。方法采用免疫组织化学SP法检测p57kip2与cyclinD1在41例上皮性卵巢癌,12例交界性肿瘤,24例良性肿瘤与12例正常卵巢组织中的表达。结果p57kip2和cy-clinD1在正常卵巢、良性、交界性、恶性肿瘤组织中的阳性率分别为91.7%(11/12)、79.2%(19/24)、58.3%(7/12)、46.3%(19/41)和8.3%(1/12)、29.2%(7/24)、50%(6/12)、75.6%(31/41),其中正常组与恶性组之间,良性与恶性组之间差异有统计学意义(P<0.05)。在卵巢癌中p57kip2和cyclinD1的表达与肿瘤分化程度,临床分期和有无淋巴结转移有关,且两者的表达呈负相关(r=-0.311,P<0.05)。结论p57kip2和cyclinD1可能共同参与了上皮性卵巢肿瘤的发生与发展,p57kip2的低表达甚至缺失和cyclinD1高表达对预测卵巢肿瘤的恶性程度及预后有指导意义。 Objeetive To investigate the relationship of p57^kip2 and cyclin D1 expressions with clinicopathological features of epithelial ovarian tumor. Methods SP immunohistochemical technique was applied to detect the expressions of p57^kip2 and cyclin D1 proteins in tissues of 41 patients with malignant epithelial ovarian cancer, 12 with borderline tumor, 24 with benign tumor and 12 normal ovaries. Results The positive-expression of p57^kip2 and cyelin D1 was 91.7%(11/12), 79. 2%(19/24), 58.3%(7/12), 46. 3% (19/41) and 8. 3%(1/12), 29. 2% (7/24), 50% (6/12), 75.6% (31/41), respectively in normal, benign, borderline, and malignant tissues. There were significant differences between p57^kip2 and cyclin DI proteins in normal group compared with the malignant, and the benign compared with the malignant. In malignant ovarian tumors, overexpression of eyclin D1 and low-expression of p57^kip2 are significantly associated with high tumor grade, advanced clinical stage, and lymph node metastasis. Expression of cyclin D1 was negatively correlated with expression of p57^kip2. Conclusion p57^kip2 and cyclin D1 played important roles in occurrence and development of epithelial ovarian cancer. Overexpression of eyclin D1 and low-expression of p57^kip2 provide important implications of malignancy and prognosis for epithelial ovarian carcinoma.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2010年第3期330-333,共4页 Cancer Research on Prevention and Treatment
关键词 P57^KIP2 CYCLIN D1 卵巢肿瘤 p57^kip2 Cyclin D1 Ovarian carcinoma
  • 相关文献

参考文献3

二级参考文献24

  • 1Sherr CJ. The Pezcoller Lecture: Cancer cell cycles revisited [J]. Cancer Res,2000,60:3689-3695.
  • 2Sherr CJ. Cancer cell cycles[J]. Science, 1996, 274: 1672-1677.
  • 3Tavassoli FA,Devilee P. WHO classification of tumours. Pathology & genetics,tumours of the breast and female genital organs[M]. Lyon: IARC Press, 2003:10-19.
  • 4Matsuoka S, Edwards MC, Bai C,et al. p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene[J]. Genes Dev, 1995,9:650-662.
  • 5Nijjar T,Wigington D,Garbe JC,et al. p57KIP2 expression and loss of heterozygosity during immortal conversion of cultured human mammary epithelial cells [J]. Cancer Res, 1999, 59:5112-5118.
  • 6Ito Y,Takeda T,Sakon M,et al. Expression of p57/Kip2 protein in hepatocellular carcinoma[J]. Oncology, 2001,61 (3) :221-225.
  • 7Koff A,Cross F,Fisher A,et al. Human cyclin E,a new cyclin that interacts with two members of the CDC2 gene family[J].Cell, 1991,66:1217-1228.
  • 8Schraml P,Bucher C, Bissig H, et al. Cyclin E overexpression and amplification in human tumours[J]. J Pathol, 2003,200 (3) :375-382.
  • 9Bortner DM,Rosenberg MP. Induction of mammary gland hyperplasia and carcinomas in transgenic mice expressing human cyclin E[J]. Mol Cell Biol, 1997,17: 453-459.
  • 10Sakaguchi T;Watanabe A;SawadaH;Yamada Y,Yamashita J,Matsuda M,Nakajima M,Miwa T,Hirao T,Nakano H.Prognostic value of cyclin E and p53 expression in gastric carcinoma[J],1998(7).

共引文献38

同被引文献10

  • 1STAAL SP. Molecular cloning of the akt oncogene and its human Homologues AKT1 and AKT2: amp lification of AKT1 in a primary human gastric adenocarcinoma [ J ]. Proc Natl Acad Sci USA, 1987,84(14) :5034 - 5037.
  • 2WEST KA, CASTILLO SS, DENN IS PA. Activat ion of the PI3K/Akt pathway and chemotherapeutic resistance [ J]. Drug Res,2002,5 (6) :234 - 248.
  • 3LIAO DJ, THAKUR A, WU J, et al. Perspectives on c-myc, cyclinD1 and their interaction in cancer formation, progress-ion, and response to cheroot herapy [ J]. Crit Rev Oncog, 2007,13 (2) :93 - 158.
  • 4GUSTIN JA, OZES ON, AKCA H, et al. Cell type-specific expression of the Ikappa B kinase determines the significance of phosphatidylinositol 3-kinase/AKT signaling to NF-kappa B activation [ J ]. J Biol Chem,2004,279 ( 3 ) : 1615 - 1620.
  • 5ROBEY RB, HAY N. Mitochondrial hexokinases, novel mediators of the antiapoptotic effects of growth factors and Akt [ J ]. Oncogene,2006,25 (34) :4683 - 4696.
  • 6MAURER U, CHARVET C, WAGMAN AS, et al. Glycogen synthase Kinase-3 regulates mitochondrial outer membrane permeabilization and apoptosis by destabilization of MCL1 [ J ]. Mol Cell,2006,21 (6) :749 -760.
  • 7DUMMLER B, HEMMINGS BA. Physiological roles of PKB/Akt isoforms in development and disease [ J ]. Biochem Soc Trans, 2007,35(2) :231 -235.
  • 8MANNING BD, CANTLEY LC. AKT/PKB signaling: navigating downstream [ J ]. Cell,2007,129 (7) : 1261 - 1274.
  • 9陈胜民,潘晓琳,李锋.PI3K/Akt信号通路与卵巢癌的关系[J].国际肿瘤学杂志,2011,38(2):155-157. 被引量:6
  • 10王一,连小云,张玎,王歧山.抑制Cyclin D1基因对K562细胞生长和Vp16敏感性的影响[J].河北医科大学学报,2012,33(9):1008-1011. 被引量:1

引证文献1

二级引证文献1

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