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巴雷特食管良性、癌前和肿瘤性病变中TGR5的表达:病例系列及研究结果

TGR5 expression in benign, preneoplastic and neoplastic lesions of Barrett's esophagus: Case series and findings.

作者信息

Marketkar Shivali, Li Dan, Yang Dongfang, Cao Weibiao

机构信息

Shivali Marketkar, Dongfang Yang, Weibiao Cao, Department of Pathology, Rhode Island Hospital and Warren Alpert Medical School of Brown University, Providence, RI 02903, United States.

出版信息

World J Gastroenterol. 2017 Feb 28;23(8):1338-1344. doi: 10.3748/wjg.v23.i8.1338.


DOI:10.3748/wjg.v23.i8.1338
PMID:28293080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5330818/
Abstract

AIM: To examined the bile acid receptor TGR5 expression in squamous mucosa, Barrett's mucosa, dysplasia and esophageal adenocarcinoma (EA). METHODS: Slides were stained with TGR5 antibody. The staining intensity was scored as 1+, 2+ and 3+. The extent of staining (percentage of cells staining) was scored as follows: 1+, 1%-10%, 2+, 11%-50%, 3+, 51%-100%. A combined score of intensity and extent was calculated and categorized as negative, weak, moderate and strong staining. TGR5 mRNA was measured by real time PCR. RESULTS: We found that levels of TGR5 mRNA were significantly increased in Barrett's dysplastic cell line CP-D and EA cell line SK-GT-4, when compared with Barrett's cell line CP-A. Moderate to strong TGR5 staining was significantly higher in high-grade dysplasia and EA cases than in Barrett's esophagus (BE) or in low-grade dysplasia. Moderate to strong staining was slightly higher in low-grade dysplasia than in BE mucosa, but there is no statistical significance. TGR5 staining had no significant difference between high-grade dysplasia and EA. In addition, TGR5 staining intensity was not associated with the clinical stage, the pathological stage and the status of lymph node metastasis. CONCLUSION: We conclude that TGR5 immunostaining was much stronger in high-grade dysplasia and EA than in BE mucosa or low-grade dysplasia and that its staining intensity was not associated with the clinical stage, the pathological stage and the status of lymph node metastasis. TGR5 might be a potential marker for the progression from BE to high-grade dysplasia and EA.

摘要

目的:检测胆汁酸受体TGR5在鳞状黏膜、巴雷特黏膜、发育异常组织及食管腺癌(EA)中的表达。 方法:玻片用TGR5抗体染色。染色强度评分为1+、2+和3+。染色范围(染色细胞百分比)评分如下:1+,1%-10%;2+,11%-50%;3+,51%-100%。计算强度和范围的综合评分,并分为阴性、弱阳性、中度阳性和强阳性染色。通过实时PCR检测TGR5 mRNA。 结果:我们发现,与巴雷特细胞系CP-A相比,巴雷特发育异常细胞系CP-D和食管腺癌细胞系SK-GT-4中的TGR5 mRNA水平显著升高。高级别发育异常和食管腺癌病例中的中度至强TGR5染色显著高于巴雷特食管(BE)或低级别发育异常。低级别发育异常中的中度至强染色略高于BE黏膜,但无统计学意义。高级别发育异常和食管腺癌之间的TGR5染色无显著差异。此外,TGR5染色强度与临床分期、病理分期及淋巴结转移状态无关。 结论:我们得出结论,高级别发育异常和食管腺癌中的TGR5免疫染色比BE黏膜或低级别发育异常中的要强得多,且其染色强度与临床分期、病理分期及淋巴结转移状态无关。TGR5可能是BE进展为高级别发育异常和食管腺癌的潜在标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2817/5330818/d001829783d7/WJG-23-1338-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2817/5330818/8df3fb294fd6/WJG-23-1338-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2817/5330818/d001829783d7/WJG-23-1338-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2817/5330818/8df3fb294fd6/WJG-23-1338-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2817/5330818/d001829783d7/WJG-23-1338-g002.jpg

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引用本文的文献

[1]
Expression and significance of CDX2, FXR, and TGR5 in esophageal cancer.

Int J Clin Exp Pathol. 2022-9-15

本文引用的文献

[1]
Bile acid receptor TGR5, NADPH Oxidase NOX5-S and CREB Mediate Bile Acid-Induced DNA Damage In Barrett's Esophageal Adenocarcinoma Cells.

Sci Rep. 2016-8-11

[2]
The bile acid receptor GPBAR1 (TGR5) is expressed in human gastric cancers and promotes epithelial-mesenchymal transition in gastric cancer cell lines.

Oncotarget. 2016-9-20

[3]
Rho Kinase ROCK2 Mediates Acid-Induced NADPH Oxidase NOX5-S Expression in Human Esophageal Adenocarcinoma Cells.

PLoS One. 2016-2-22

[4]
TGR5 is essential for bile acid-dependent cholangiocyte proliferation in vivo and in vitro.

Gut. 2015-9-29

[5]
In Barrett's esophagus patients and Barrett's cell lines, ursodeoxycholic acid increases antioxidant expression and prevents DNA damage by bile acids.

Am J Physiol Gastrointest Liver Physiol. 2014-5-22

[6]
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Am J Physiol Cell Physiol. 2013-9-11

[7]
Oesophageal carcinoma.

Lancet. 2013-2-2

[8]
Trends in esophageal adenocarcinoma incidence and mortality.

Cancer. 2012-12-11

[9]
Risk factors in the development of esophageal adenocarcinoma.

Am J Gastroenterol. 2012-12-18

[10]
Expression of bile acid receptor TGR5 in gastric adenocarcinoma.

Am J Physiol Gastrointest Liver Physiol. 2012-12-13

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