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源自滤泡上皮的甲状腺肿瘤中S100A10的表达:对间变性癌侵袭性特征的作用。

S100A10 expression in thyroid neoplasms originating from the follicular epithelium: contribution to the aggressive characteristic of anaplastic carcinoma.

作者信息

Ito Yasuhiro, Arai Kazumori, Nozawa Ryushi, Yoshida Hiroshi, Higashiyama Takuya, Takamura Yuuki, Miya Akihiro, Kobayashi Kaoru, Kuma Kanji, Miyauchi Akira

机构信息

Kuma Hospital, Kobe, Japan.

出版信息

Anticancer Res. 2007 Jul-Aug;27(4C):2679-83.

Abstract

BACKGROUND

S100A10, a member of the S100 family, forms a heterotetramer with annexin IIH and promotes carcinoma invasion and metastasis by plasminogen activation. In this study, S100A10 and annexin II expression in thyroid neoplasms were demonstrated.

PATIENTS AND METHODS

The expression levels of S100A10 and annexin II in 193 thyroid neoplasms were immunohistochemically investigated.

RESULTS

S10A10 and annexin II were not expressed in normal follicular cells or any follicular adenomas. Cells stained positively in 14.6% and 20.8% of follicular carcinomas for S100A10 and annexin II, respectively, but their expression levels were always low. S100A10 and annexin II were expressed in all papillary carcinomas, but 88.2% and 82.8% ofpapillary carcinomas were classified in the low group. These expression levels were not linked to any clinicopathological features. S100S10 and annexin II were also expressed in all anaplastic carcinomas, with 83.3% of these lesions were classified in the high group.

CONCLUSION

These findings suggest that S100A10 and annexin II contribute to the aggressive characteristics of anaplastic carcinoma, while playing a constitutive role in papillary carcinoma.

摘要

背景

S100A10是S100家族成员,与膜联蛋白IIH形成异源四聚体,并通过纤溶酶原激活促进癌侵袭和转移。本研究检测了甲状腺肿瘤中S100A10和膜联蛋白II的表达情况。

患者和方法

采用免疫组织化学方法检测193例甲状腺肿瘤中S100A10和膜联蛋白II的表达水平。

结果

正常滤泡细胞或任何滤泡性腺瘤中均未检测到S10A10和膜联蛋白II表达。在14.6%的滤泡癌中,S100A10呈阳性染色,在20.8%的滤泡癌中,膜联蛋白II呈阳性染色,但它们的表达水平始终较低。所有乳头状癌中均检测到S100A10和膜联蛋白II表达,但88.2%和82.8%的乳头状癌被归类为低表达组。这些表达水平与任何临床病理特征均无关联。所有未分化癌中也检测到S100S10和膜联蛋白II表达,其中83.3%的病变被归类为高表达组。

结论

这些发现表明,S100A10和膜联蛋白II促成了未分化癌的侵袭性特征,而在乳头状癌中发挥组成性作用。

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