• 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

原发性肿瘤及其相应远处转移灶中的c-Met表达。

c-Met expression in primary tumors and their corresponding distant metastases.

作者信息

Isaksson-Mettävainio Martin, Van Guelpen Bethany, Oberg Ake, Stenling Roger, Palmqvist Richard, Henriksson Maria L

机构信息

Department of Medical Biosciences and Pathology, Umeå University, SE-901 85 Umeå, Sweden.

出版信息

Mol Med Rep. 2008 Nov-Dec;1(6):787-90. doi: 10.3892/mmr_00000029.

DOI:10.3892/mmr_00000029
PMID:21479486
Abstract

c-Met is a receptor tyrosine kinase that has been implicated in the pathogenesis and growth of a wide variety of human malignancies, including CRC, but its role in metastasis is largely unknown. We compared c-Met expression in primary human colorectal carcinomas and distant metastases from the same patients. Formalin-fixed paraffin-embedded tissue samples from 69 colorectal cancer patients were obtained. The protein expression of c-Met was evaluated immunohistochemically using a commercial antibody. The difference in expression between primary tumors and their corresponding distant metastases was analyzed using the Wilcoxon signed-rank test. c-Met expression was statistically significantly lower in the distant metastases compared to their corresponding primary tumors (p<0.001), whereas no difference was found between lymph node metastases and their corresponding primary tumors (p=0.957). The degree of c-Met expression was not related to clinicopathological characteristics such as tumor grade and Dukes' stage at the time of primary tumor diagnosis, or to the location of the distant metastases. We demonstrated that c-Met expression is often reduced in distant metastases compared to their corresponding primary colorectal tumors. Additional studies of c-Met activation and signal transduction will increase our knowledge about the role of c-Met in colorectal cancer metastasis.

摘要

c-Met是一种受体酪氨酸激酶,已被证实与包括结直肠癌(CRC)在内的多种人类恶性肿瘤的发病机制和生长有关,但其在转移过程中的作用仍 largely unknown。我们比较了原发性人类结直肠癌及其来自同一患者的远处转移灶中c-Met的表达情况。获取了69例结直肠癌患者的福尔马林固定石蜡包埋组织样本。使用商业抗体通过免疫组织化学方法评估c-Met的蛋白表达。采用Wilcoxon符号秩检验分析原发性肿瘤与其相应远处转移灶之间的表达差异。与相应的原发性肿瘤相比,远处转移灶中c-Met的表达在统计学上显著降低(p<0.001),而淋巴结转移灶与其相应的原发性肿瘤之间未发现差异(p=0.957)。c-Met的表达程度与原发性肿瘤诊断时的肿瘤分级和Dukes分期等临床病理特征无关,也与远处转移灶的位置无关。我们证明,与相应的原发性结直肠肿瘤相比,远处转移灶中c-Met的表达通常会降低。对c-Met激活和信号转导的进一步研究将增加我们对c-Met在结直肠癌转移中作用的认识。

相似文献

1
c-Met expression in primary tumors and their corresponding distant metastases.原发性肿瘤及其相应远处转移灶中的c-Met表达。
Mol Med Rep. 2008 Nov-Dec;1(6):787-90. doi: 10.3892/mmr_00000029.
2
Delayed regional metastases, distant metastases, and second primary malignancies in squamous cell carcinomas of the larynx and hypopharynx.喉和下咽鳞状细胞癌的区域转移延迟、远处转移及第二原发性恶性肿瘤
Laryngoscope. 2001 Jun;111(6):1079-87. doi: 10.1097/00005537-200106000-00028.
3
Differences in AgNOR quantity between colorectal cancer and corresponding metastases: are they useful for prognostic purposes?结直肠癌与相应转移灶之间银染核仁组织区(AgNOR)数量的差异:它们对预后评估有帮助吗?
Eur J Histochem. 1997;41(2):111-8.
4
Topoisomerase I protein expression in primary colorectal cancer and lymph node metastases.拓扑异构酶I蛋白在原发性结直肠癌及淋巴结转移灶中的表达
Hum Pathol. 2002 Nov;33(11):1114-9. doi: 10.1053/hupa.2002.129202.
5
Clinical relevance of transforming growth factor alpha, epidermal growth factor receptor, p53, and Ki67 in colorectal liver metastases and corresponding primary tumors.转化生长因子α、表皮生长因子受体、p53和Ki67在结直肠癌肝转移及相应原发性肿瘤中的临床相关性
Hepatology. 1998 Oct;28(4):971-9. doi: 10.1002/hep.510280411.
6
Overexpression of focal adhesion kinase in primary colorectal carcinomas and colorectal liver metastases: immunohistochemistry and real-time PCR analyses.原发性结直肠癌及结直肠癌肝转移灶中粘着斑激酶的过表达:免疫组织化学和实时聚合酶链反应分析
Clin Cancer Res. 2003 Jan;9(1):215-22.
7
Deleted in colon cancer protein expression in colorectal cancer metastases: a major predictor of survival in patients with unresectable metastatic disease receiving palliative fluorouracil-based chemotherapy.结肠癌缺失蛋白在结直肠癌转移灶中的表达:接受以氟尿嘧啶为基础的姑息化疗的不可切除转移性疾病患者生存的主要预测指标。
J Clin Oncol. 2004 Sep 15;22(18):3758-65. doi: 10.1200/JCO.2004.08.066.
8
c-MET expression level in primary colon cancer: a predictor of tumor invasion and lymph node metastases.原发性结肠癌中c-MET的表达水平:肿瘤侵袭和淋巴结转移的一个预测指标
Clin Cancer Res. 2003 Apr;9(4):1480-8.
9
Expression of E-cadherin in human ductal breast cancer carcinoma in situ, invasive carcinomas, their lymph node metastases, their distant metastases, carcinomas with recurrence and in recurrence.E-钙黏蛋白在人乳腺导管原位癌、浸润性癌、其淋巴结转移灶、远处转移灶、复发性癌及复发中的表达
Anticancer Res. 2007 Jul-Aug;27(4A):1969-74.
10
High epidermal growth factor receptor expression in metastatic colorectal cancer lymph nodes may be more prognostic of poor survival than in primary tumor.转移性结直肠癌淋巴结中表皮生长因子受体的高表达可能比原发性肿瘤更能预示生存不良。
Am J Clin Oncol. 2009 Jun;32(3):245-52. doi: 10.1097/COC.0b013e3181891326.

引用本文的文献

1
TR1801-ADC: a highly potent cMet antibody-drug conjugate with high activity in patient-derived xenograft models of solid tumors.TR1801-ADC:一种高效力的 cMet 抗体药物偶联物,在固体肿瘤患者来源的异种移植模型中具有高活性。
Mol Oncol. 2020 Jan;14(1):54-68. doi: 10.1002/1878-0261.12600. Epub 2019 Dec 3.
2
c-MET expression in colorectal adenomas and primary carcinomas with its corresponding metastases.c-MET在结直肠腺瘤、原发性癌及其相应转移灶中的表达。
J Gastrointest Oncol. 2015 Dec;6(6):618-27. doi: 10.3978/j.issn.2078-6891.2015.072.
3
Clinical impact of c-MET expression and genetic mutational status in colorectal cancer patients after liver resection.
c-MET表达及基因变异状态对结直肠癌肝切除术后患者的临床影响
Cancer Sci. 2014 Aug;105(8):1002-7. doi: 10.1111/cas.12453. Epub 2014 Aug 7.
4
Expression of HGF and Met in human tissues of colorectal cancers: biological and clinical implications for synchronous liver metastasis.HGF 和 Met 在人结直肠癌组织中的表达:对同步肝转移的生物学和临床意义。
Int J Med Sci. 2013;10(5):548-59. doi: 10.7150/ijms.5191. Epub 2013 Mar 15.