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ZEB1在食管鳞状细胞癌和小细胞癌中的细胞核、细胞质及基质表达。

Nuclear, cytoplasmic, and stromal expression of ZEB1 in squamous and small cell carcinoma of the esophagus.

作者信息

Goscinski Mariusz Adam, Xu Ruiping, Zhou Fuyou, Wang Junsheng, Yang Haijun, Huang Ruixia, Li Yaqing, Larsen Stein Gunnar, Giercksky Karl-Erik, Nesland Jahn Marthin, Suo Zhenhe

机构信息

Department of Surgery, The Norwegian Radium Hospital, Oslo University Hospital, Institute for Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.

Department of Oncology, Anyang Tumor Hospital, Anyang, Henan Province, China.

出版信息

APMIS. 2015 Dec;123(12):1040-7. doi: 10.1111/apm.12473.

Abstract

Zinc finger E-box-binding homeobox 1 (ZEB1) is a transcriptional factor known to repress E-cadherin promoter and thus induce EMT. Expression of ZEB-1 has in numerous cancers been associated with aggressive disease and poor clinical outcome. Our aim was to investigate the expression of ZEB1 in esophageal squamous- and small-cell carcinomas. Immunohistochemical staining was performed on tissue sections obtained from 151 patients with esophageal squamous cell carcinoma (ESCC) and 25 patients with primary small-cell carcinoma of the esophagus (PSCCE). Semi-quantitative analysis, and thus statistical analysis, has been accomplished on the samples. Immunohistochemistry revealed ZEB1 expression in the cytoplasm (64.9% of cases), in nuclei (11.3% of cases) and in tumor stroma (80.1% of cases) of ESCC. In PSCCE only nuclear staining (88.0% of cases) was observed. Weak cytoplasmic expression of ZEB1 in ESCC was associated with longer survival. Immunohistochemical evaluation of ZEB1 cytoplasmic expression in ESCC may have clinical prognostic value, but further studies are needed to fully understand the function as well as potential clinical and therapeutic implications of ZEB1 expression in cancers.

摘要

锌指E盒结合同源框1(ZEB1)是一种转录因子,已知其可抑制E-钙黏蛋白启动子,从而诱导上皮-间质转化(EMT)。在众多癌症中,ZEB-1的表达与疾病侵袭性和不良临床预后相关。我们的目的是研究ZEB1在食管鳞状细胞癌和小细胞癌中的表达情况。对151例食管鳞状细胞癌(ESCC)患者和25例原发性食管小细胞癌(PSCCE)患者的组织切片进行了免疫组织化学染色。对样本进行了半定量分析,进而完成了统计分析。免疫组织化学显示,ESCC的细胞质(64.9%的病例)、细胞核(11.3%的病例)和肿瘤基质(80.1%的病例)中存在ZEB1表达。在PSCCE中仅观察到细胞核染色(88.0%的病例)。ESCC中ZEB1的弱细胞质表达与更长的生存期相关。对ESCC中ZEB1细胞质表达进行免疫组织化学评估可能具有临床预后价值,但需要进一步研究以充分了解ZEB1在癌症中的功能以及潜在的临床和治疗意义。

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