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CD44v6在肠型和弥漫型胃癌转移灶中的差异表达。

Differential expression of CD44v6 in metastases of intestinal and diffuse types of gastric carcinoma.

作者信息

Castellà E M, Ariza A, Pellicer I, Fernández-Vasalo A, Ojanguren I

机构信息

Department of Pathology, Hospital Germans Trias I Pujol, Autonomous University of Barcelona, Spain.

出版信息

J Clin Pathol. 1998 Feb;51(2):134-7. doi: 10.1136/jcp.51.2.134.

Abstract

AIMS

To assess whether standard and variant isoforms of CD44 (CD44s, CD44v5, and CD44v6) have a differential expression profile in early versus advanced gastric adenocarcinoma of the diffuse and intestinal types and their metastases.

METHODS

Immunohistochemical expression of CD44s, CD44v5, and CD44v6 was evaluated in 14 early gastric cancers (nine intestinal and five diffuse) and 37 advanced adenocarcinomas (21 intestinal and 16 diffuse) as well as in 18 cases of perigastric lymph node metastasis. Ten normal and five metaplastic gastric mucosa samples were also included in the study.

RESULTS

Although no significant association was found between the degree of invasion and the CD44 expression profile, CD44v6 positivity was detected more frequently in metastases of intestinal-type carcinomas (66%) than in metastases of diffuse-type neoplasms (11%) (p < 0.05). Weak CD44s, CD44v5, and CD44v6 expression was observed focally in both normal and metaplastic gastric mucosa samples.

CONCLUSIONS

These data suggest that CD44v6 expression may be involved in the production of lymph node metastases in intestinal-type gastric carcinoma but not in the diffuse-type disease, the metastatic potential of which is most likely unrelated to the CD44 family of adhesion molecules.

摘要

目的

评估CD44的标准和变异亚型(CD44s、CD44v5和CD44v6)在弥漫型和肠型早期与进展期胃腺癌及其转移灶中是否具有不同的表达谱。

方法

对14例早期胃癌(9例肠型和5例弥漫型)、37例进展期腺癌(21例肠型和16例弥漫型)以及18例胃周淋巴结转移病例进行CD44s、CD44v5和CD44v6的免疫组化表达评估。研究还纳入了10例正常胃黏膜样本和5例化生胃黏膜样本。

结果

虽然未发现侵袭程度与CD44表达谱之间存在显著关联,但在肠型癌转移灶中检测到CD44v6阳性的频率(66%)高于弥漫型肿瘤转移灶(11%)(p<0.05)。在正常和化生胃黏膜样本中均局灶性观察到CD44s、CD44v5和CD44v6的弱表达。

结论

这些数据表明,CD44v6表达可能参与肠型胃癌的淋巴结转移形成,但不参与弥漫型疾病的转移,弥漫型疾病的转移潜能很可能与CD44黏附分子家族无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c343/500508/c1e49a62101c/jclinpath00263-0046-a.jpg

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