国际病理科学与临床杂志 2009, 29(6) 478-482 DOI:     ISSN: 1673-2588 CN: 43-1458/R

本期目录 | 下期目录 | 过刊浏览 | 高级检索                                                            [打印本页]   [关闭]
综述
扩展功能
本文信息
Supporting info
PDF(1008KB)
[HTML全文]
参考文献[PDF]
参考文献
服务与反馈
把本文推荐给朋友
加入我的书架
加入引用管理器
引用本文
Email Alert
文章反馈
浏览反馈信息
本文关键词相关文章
上皮型钙黏蛋白
胃癌
弥漫型胃癌
本文作者相关文章
PubMed
上皮型钙黏蛋白与散发性弥漫型胃癌
张宝燕综述 李向红审校
中国人民解放军总医院病理科, 北京 100853
摘要

胃癌在世界范围内发病率高,死亡率也高,近些年肠型胃癌发病率有所下降,但弥漫型胃癌发病率不降反升。已知上皮型钙黏蛋白(E-cadherin, E-cd)与肿瘤的发生、侵袭和转移有关。E-cd胚系突变是遗传性弥漫型胃癌发病的遗传学基础,散发性弥漫型胃癌中常见其表达下调,但其下调的临床病理意义尤其是预后意义仍无定论。本文对E-cd在散发性弥漫型胃癌的表达情况及其下调机制进行了综述。

关键词 上皮型钙黏蛋白   胃癌   弥漫型胃癌  
E-cadherin and sporadic diffuse gastric carcinoma
 ZHANG Baoyan, LI Xianghong
Department of Pathology, Chinese PLA General Hospital, Beijing 100853, China
Abstract:

Gastric carcinoma(GC) is highly prevalent worldwide with a high rate of death. Although the incidence of intestinal GC has declined gradually, the incidence of diffuse GC has remained stable or even increased. It was well established that E-cadherin(E-cd) loss is involved in tumor initiation, infiltration and metastasis. E-cd germ line mutation is the genetic foundation for the hereditary diffuse GC. The down-regulation of E-cd expression was also observed in sporadic diffuse GC, yet its clinicopathologic significance, particularly to the prognosis of GC remains largely unknown. In this article, we reviewed expression pattern of E-cd in sporadic GC and its significance. The molecular mechanisms responsible for E-cd down-regulation in sporadic diffuse GC were also discussed.

Keywords: E-cadherin;gastric carcinoma;sporadic;diffuse  
收稿日期 2009-10-16 修回日期 2009-12-11 网络版发布日期  
DOI:
基金项目:

通讯作者: 李向红
作者简介:
作者Email: xhli72@yahoo.com.cn

参考文献:

[1]Crew KD, Neugut AI. Epidemiology of gastric cancer[J]. World J Gastroenterol, 2006,12(3):354-362.
[2]Henson DE, Dittus C, Younes M, et al. Differential trends in the intestinal and diffuse types of gastric carcinoma in the United States, 1973-2000: increase in the signet ring cell type[J]. Arch Pathol Lab Med, 2004,128(7):765-770.
[3]Hamilton SR, Aaltonen LA. Pathology and Genetics of Tumours of the Digestive System[M]. Lyon: IARC Press,2000:42-45.
[4]Ekstrom AM, Serafini M, Nyren O, et al. Dietary antioxidant intake and the risk of cardia cancer and noncardia cancer of the intestinal and diffuse types: a population-based case-control study in Sweden[J]. Int J Cancer, 2000,87(1):133-140.
[5]Chan AO. E-cadherin in gastric cancer[J]. World J Gastroenterol, 2006,12(2):199-203.
[6]Yoon CS, Hyung WJ, Lee JH, et al. Expression of S100A4, E-cadherin, alpha- and beta-catenin in gastric adenocarcinoma[J]. Hepatogastroenterology, 2008,55(86-87):1916-1920.
[7]Arévalo F, Monge E, Morales D. E-cadherin molecular expresion in the diffuse and intestinal types of gastric adenocarcinoma. A report from Lima, Peru[J]. Rev Esp Enferm Dig, 2007,99(6):325-329.
[8]Walch A, Seidl S, Hermannstdter C, et al. Combined analysis of Rac1, IQGAP1, Tiam1 and E-cadherin expression in gastric cancer[J]. Mod Pathol, 2008,21(5):544-552.
[9]Guzmán P, Araya J, Villaseca M, et al. Immunohistochemical expression of the E-cadherin-catenin complex in gastric cancer[J]. Rev Med Chil, 2006,134(8):1002-1009.
[10]Lee KH, Shin SJ, Kim KO, et al. Relationship between E-cadherin, matrix metalloproteinase-7 gene expression and clinicopathological features in gastric carcinoma[J]. Oncol Rep, 2006,16(4):823-830.
[11]Zhong XY, Zhang LH, Jia SQ, et al. Positive association of up-regulated Cripto-1 and down-regulated E-cadherin with tumour progression and poor prognosis in gastric cancer[J]. Histopathology, 2008,52(5):560-568.
[12]Kim JH, Park JM, Jung CW, et al. The significances of lymph node micrometastasis and its correlation with E-cadherin expression in pT1-T3N0 gastric adenocarcinoma[J]. J Surg Oncol, 2008,97(2):125-130.
[13]Kim DY, Joo JK, Park YK, et al. E-cadherin expression in early gastric carcinoma and correlation with lymph node metastasis[J]. J Surg Oncol, 2007,96(5):429-435.
[14]Aoki R, Yasuda M, Torisu R, et al. Relationship between lymph node metastasis and E-cadherin expression in submucosal invasive gastric carcinomas with gastric-phenotype[J]. J Med Invest, 2007,54(1-2):159-167.
[15]Boo YJ, Park SS, Kim JH, et al. Gastric neuroendocrine carcinoma: clinicopathologic review and immunohistochemical study of E-cadherin and Ki-67 as prognostic markers[J]. J Surg Oncol, 2007,95(2):110-117.
[16]Theuer CP, Al-Kuran R, Akiyama Y, et al. Increased epithelial cadherin expression among Japanese intestinal-type gastric cancers compared with specimens from American patients of European descent[J]. Am Surg, 2006,72(4):332-338.
[17]Berx G, Becker KF, Hofler H, et al. Mutations of the human E-cadherin (CDH1) gene[J]. Hum Mutat, 1998,12(4):226-237.
[18]Costello JF, Plass C. Methylation matters[J]. J Med Genet, 2001, 38(5):285-303.
[19]Wang L, Zhang F, Wu PP, et al. Disordered beta-catenin expression and E-cadherin/CDH1 promoter methylation in gastric carcinoma[J]. World J Gastroenterol, 2006,12(26):4228-4231.
[20]Zazula M, Ferreira AM, Czopek JP, et al. CDH1 gene promoter hypermethylation in gastric cancer: relationship to Goseki grading, microsatellite instability status, and EBV invasion[J]. Diagn Mol Pathol, 2006,15(1):24-29.
[21]Ikoma H, Ichikawa D, Koike H, et al. Correlation between serum DNA methylation and prognosis in gastric cancer patients[J]. Anticancer Res, 2006,26(3B):2313-2316.
[22]Liu YC, Shen CY, Wu HS, et al. Mechanisms inactivating the gene for E-cadherin in sporadic gastric carcinomas[J]. World J Gastroenterol, 2006,12(14):2168-2173.
[23]Korpal M, Lee ES, Hu G, et al. The miR-200 family inhibits epithelial-mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2[J]. J Biol Chem, 2008,283(22):14910-14914.
[24]Nakada C, Matsuura K, Tsukamoto Y, et al. Genome-wide microRNA expression profiling in renal cell carcinoma: significant down-regulation of miR-141 and miR-200c[J]. J Pathol, 2008,216(4):418-427.
[25]Gandellini P, Folini M, Longoni N, et al. miR-205 exerts tumor-suppressive functions in human prostate through down-regulation of protein kinase Cepsilon[J]. Cancer Res, 2009,69(6):2287-2295.
[26]Park SM, Gaur AB, Lengyel E, et al. The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2[J]. Genes Dev, 2008,22(7):894-907.
[27]Gregory PA, Bert AG, Paterson EL, et al. The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1[J]. Nat Cell Biol, 2008,10(5):593-601.
[28]Nakada C, Matsuura K, Tsukamoto Y, et al. Genome-wide microRNA expression profiling in renal cell carcinoma: significant down-regulation of miR-141 and miR-200c[J]. J Pathol, 2008,216(4):418-427.
[29]Hurteau GJ, Carlson JA, Spivack SD, et al. Overexpression of the microRNA hsa-miR-200c leads to reduced expression of transcription factor 8 and increased expression of E-cadherin[J]. Cancer Res, 2007,67(17):7972-7976.
[30]Hurteau GJ, Carlson JA, Roos E, et al. Stable expression of miR-200c alone is sufficient to regulate TCF8 (ZEB1) and restore E-cadherin expression[J]. Cell Cycle, 2009, 8(13): 2064-2069.
[31]Place RF, Li LC, Pookot D, et al. MicroRNA-373 induces expression of genes with complementary promoter sequences[J]. Proc Natl Acad Sci USA, 2008,105(5):1608-1613.

本刊中的类似文章
1.唐春莲;姚根有.胃癌伴神经内分泌分化的研究进展[J]. 国际病理科学与临床杂志, 2007,27(2): 9-132
2.黄大兵综述 胡世莲审校.RUNX3基因与胃癌的关系[J]. 国际病理科学与临床杂志, 2008,28(6): 6-490
3.邱秀琴综述 石巍 审校.胃癌相关抑癌基因甲基化研究进展[J]. 国际病理科学与临床杂志, 2008,28(5): 6-398
4.邵伟伟1,何松2; 王东林1.胃癌细胞DNA含量和倍体分析的研究进展[J]. 国际病理科学与临床杂志, 2006,26(3): 3-195
5.王元宇;叶再元,赵仲生.胃癌侵袭与转移相关分子的研究进展[J]. 国际病理科学与临床杂志, 2006,26(4): 9-312
6.邵志滨;谢海龙.组织芯片技术及其在胃癌研究中的应用[J]. 国际病理科学与临床杂志, 2007,27(3): 12-238
7.徐胜美, 马红梅,郭东.E-cadherin在结直肠癌中的表达及其与侵袭转移的关系[J]. 国际病理科学与临床杂志, 2009,29(4): 284-288
8.王莉1,戴文香1;苏琦2.DNA甲基化和组蛋白乙酰化与胃癌的研究进展[J]. 国际病理科学与临床杂志, 2008,28(3): 10-235
9.龚晓林1, 唐建武2, 耿秀文3.Annexin A7在胃癌及转移灶中的表达及意义[J]. 国际病理科学与临床杂志, 2009,29(5): 369-373

Copyright by 国际病理科学与临床杂志