• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

bcl-2蛋白在巴雷特化生-发育异常-癌序列中的表达。

bcl-2 protein expression in the Barrett's metaplasia-dysplasia-carcinoma sequence.

作者信息

Goldblum J R, Rice T W

机构信息

Department of Anatomic Pathology, Cleveland Clinic Foundation, Ohio, USA.

出版信息

Mod Pathol. 1995 Oct;8(8):866-9.

PMID:8552577
Abstract

The bcl-2 proto-oncogene encodes a protein that blocks programmed cell death (apoptosis). Although bcl-2 has been shown to be involved in the development of follicular lymphoma via a chromosomal translocation t(14;18), little is known about its function in non-hematolymphoid neoplasms. The bcl-2 protein is normally expressed in the regenerative crypt compartment of the colon, small intestine, and stomach, and has been found to be abnormally overexpressed as an early event in the dysplasia-carcinoma sequences of both ulcerative colitis-related and gastric neoplasias. This study was undertaken to evaluate the role of bcl-2 in the Barrett's metaplasia-dysplasia-carcinoma sequence. Thirty-six esophageal resection specimens were studied, using a monoclonal antibody to the bcl-2 protein on fixed paraffin-embedded specimens. Barrett's mucosa was present in each specimen: low-grade dysplasia in 35, high-grade dysplasia in 34, intramucosal carcinoma (IMC) in 23, and submucosal carcinoma in 13. In addition, a section of the gastric resection margin was evaluated for bcl-2 immunoreactivity in each case. In all cases, the regenerative compartment of the gastric mucosa in the resection margins stained for bcl-2; however, no immunoreactivity was seen in any of the cases of Barrett's mucosa with or without dysplasia or carcinoma. We conclude that, in contrast to its role in gastric neoplasia, bcl-2 alterations are not an important molecular marker in the neoplastic progression of Barrett's mucosa.

摘要

bcl-2原癌基因编码一种可阻止程序性细胞死亡(细胞凋亡)的蛋白质。尽管已证实bcl-2通过染色体易位t(14;18)参与滤泡性淋巴瘤的发生发展,但对其在非血液淋巴系统肿瘤中的功能却知之甚少。bcl-2蛋白通常在结肠、小肠和胃的再生隐窝区表达,并且已发现在溃疡性结肠炎相关肿瘤和胃肿瘤的发育异常-癌序列的早期事件中异常过度表达。本研究旨在评估bcl-2在巴雷特化生-发育异常-癌序列中的作用。使用针对固定石蜡包埋标本中bcl-2蛋白的单克隆抗体,对36例食管切除标本进行了研究。每个标本均存在巴雷特黏膜:低级别发育异常35例,高级别发育异常34例,黏膜内癌(IMC)23例,黏膜下癌13例。此外,对每个病例胃切除切缘的一部分进行bcl-2免疫反应性评估。在所有病例中,切除切缘胃黏膜的再生区bcl-2染色阳性;然而,在任何伴有或不伴有发育异常或癌的巴雷特黏膜病例中均未观察到免疫反应性。我们得出结论,与bcl-2在胃肿瘤中的作用相反, bcl-2改变在巴雷特黏膜肿瘤进展中不是一个重要的分子标志物。

相似文献

1
bcl-2 protein expression in the Barrett's metaplasia-dysplasia-carcinoma sequence.bcl-2蛋白在巴雷特化生-发育异常-癌序列中的表达。
Mod Pathol. 1995 Oct;8(8):866-9.
2
Suppression of apoptosis does not foster neoplastic growth in Barrett's esophagus.细胞凋亡的抑制不会促进巴雷特食管的肿瘤生长。
Mod Pathol. 1999 Mar;12(3):239-50.
3
High-grade dysplasia and superficial adenocarcinoma in Barrett's esophagus: histological mapping and expression of p53, p21 and Bcl-2 oncoproteins.巴雷特食管中的高级别异型增生和浅表腺癌:组织学定位及p53、p21和Bcl-2癌蛋白的表达
Virchows Arch. 2003 Jan;442(1):18-24. doi: 10.1007/s00428-002-0674-1. Epub 2002 Sep 24.
4
p53 immunoreactivity in Barrett's metaplasia, dysplasia, and adenocarcinoma--a case report.巴雷特化生、发育异常及腺癌中的p53免疫反应性——病例报告
Hepatogastroenterology. 2001 Nov-Dec;48(42):1662-4.
5
p53 gene mutation and protein accumulation during neoplastic progression in Barrett's esophagus.巴雷特食管肿瘤进展过程中的p53基因突变与蛋白积聚
Mod Pathol. 2001 May;14(5):397-403. doi: 10.1038/modpathol.3880324.
6
Gains and amplifications of c-myc, EGFR, and 20.q13 loci in the no dysplasia-dysplasia-adenocarcinoma sequence of Barrett's esophagus.巴雷特食管无发育异常-发育异常-腺癌序列中c-myc、表皮生长因子受体(EGFR)及20号染色体长臂13区(20.q13)位点的获得与扩增
Cancer Epidemiol Biomarkers Prev. 2008 Jun;17(6):1380-5. doi: 10.1158/1055-9965.EPI-07-2734.
7
Esophageal polypoid dysplasia of gastric foveolar phenotype with focal intramucosal carcinoma associated with Barrett's esophagus.伴有局灶性黏膜内癌的胃小凹型食管息肉样发育异常,与巴雷特食管相关。
Am J Surg Pathol. 2008 Oct;32(10):1581-5. doi: 10.1097/PAS.0b013e3181753aa6.
8
Activation of Akt is increased in the dysplasia-carcinoma sequence in Barrett's oesophagus and contributes to increased proliferation and inhibition of apoptosis: a histopathological and functional study.在巴雷特食管的发育异常-癌序列中,Akt的激活增加,这有助于增殖增加和细胞凋亡抑制:一项组织病理学和功能研究。
BMC Cancer. 2007 Jun 8;7:97. doi: 10.1186/1471-2407-7-97.
9
MUC4 is increased in high grade intraepithelial neoplasia in Barrett's oesophagus and is associated with a proapoptotic Bax to Bcl-2 ratio.MUC4在巴雷特食管的高级别上皮内瘤变中表达增加,且与促凋亡蛋白Bax和抗凋亡蛋白Bcl-2的比例相关。
J Clin Pathol. 2004 Dec;57(12):1267-72. doi: 10.1136/jcp.2004.017020.
10
Genetic alterations in Barrett's esophagus and esophageal adenocarcinoma.巴雷特食管和食管腺癌中的基因改变。
Minerva Chir. 2002 Dec;57(6):733-52.

引用本文的文献

1
Exercise promotes motor functional recovery in rats with corticospinal tract injury: anti-apoptosis mechanism.运动促进皮质脊髓束损伤大鼠的运动功能恢复:抗凋亡机制。
Neural Regen Res. 2015 Apr;10(4):644-50. doi: 10.4103/1673-5374.155441.
2
Signaling pathways in the molecular pathogenesis of adenocarcinomas of the esophagus and gastroesophageal junction.食管及胃食管交界腺癌分子发病机制中的信号通路
Cancer Biol Ther. 2013 Sep;14(9):782-95. doi: 10.4161/cbt.25362. Epub 2013 Jun 17.
3
Barrett's oesophagus and adenocarcinoma.巴雷特食管与腺癌。
World J Surg Oncol. 2004 May 7;2:12. doi: 10.1186/1477-7819-2-12.
4
Molecular biology of Barrett's adenocarcinoma.巴雷特腺癌的分子生物学
Ann Surg. 2001 Mar;233(3):322-37. doi: 10.1097/00000658-200103000-00005.
5
Molecular evolution of the metaplasia-dysplasia-adenocarcinoma sequence in the esophagus.食管化生-发育异常-腺癌序列的分子进化
Am J Pathol. 1999 Apr;154(4):965-73. doi: 10.1016/S0002-9440(10)65346-1.
6
Histopathological evaluation of apoptosis in cancer.癌症中细胞凋亡的组织病理学评估。
Am J Pathol. 1998 Oct;153(4):1041-53. doi: 10.1016/S0002-9440(10)65649-0.