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牙源性肿瘤中基底膜成分的表达

Expression of basement membrane components in odontogenic tumors.

作者信息

Poomsawat Sopee, Punyasingh Jirapa, Vejchapipat Paisarn

机构信息

Department of Oral Pathology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 Nov;104(5):666-75. doi: 10.1016/j.tripleo.2006.08.025. Epub 2006 Dec 5.

DOI:10.1016/j.tripleo.2006.08.025
PMID:17150384
Abstract

OBJECTIVE

The objective was to characterize the expression of BMCs (laminins 1 and 5, collagen type IV, and fibronectin) in ameloblastomas, calcifying cystic odontogenic tumors (CCOTs), and adenomatoid odontogenic tumors (AOTs).

STUDY DESIGN

BMCs were analyzed in 14 ameloblastomas, 7 CCOTs, and 7 AOTs using immunohistochemistry.

RESULTS

In normal oral mucosa, linear deposits of these proteins were found at the epithelial-mesenchymal junction, but not in epithelial cytoplasm. In all tumors studied, linear deposits of all proteins were found at the epithelial-mesenchymal junction; laminin 1 was expressed in all tumor cells, regardless of cell types. For CCOTs, laminin 5 was found faintly in suprabasal cells, but expressed strongly in ghost cells. For AOTs, laminin 5 strongly decorated tumor cells adjacent to mineralization.

CONCLUSIONS

Laminin 1 may be a marker for odontogenic epithelium. Additionally, laminin 5 may be involved in ghost cell formation and initiation of calcification.

摘要

目的

本研究旨在明确牙釉质瘤、牙源性钙化囊性肿瘤(CCOT)及牙源性腺样瘤(AOT)中基底膜成分(层粘连蛋白1和5、IV型胶原及纤连蛋白)的表达情况。

研究设计

采用免疫组织化学方法对14例牙釉质瘤、7例CCOT及7例AOT中的基底膜成分进行分析。

结果

在正常口腔黏膜中,这些蛋白呈线性沉积于上皮-间充质交界处,而非上皮细胞质中。在所研究的所有肿瘤中,所有蛋白均呈线性沉积于上皮-间充质交界处;层粘连蛋白1在所有肿瘤细胞中均有表达,与细胞类型无关。对于CCOT,层粘连蛋白5在上皮基底上层细胞中表达较弱,但在影细胞中表达较强。对于AOT,层粘连蛋白5在矿化附近的肿瘤细胞中呈强阳性表达。

结论

层粘连蛋白1可能是牙源性上皮的标志物。此外,层粘连蛋白5可能参与影细胞形成及钙化起始过程。

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Immunohistochemical expression of SPARC in odontogenic keratocysts: a comparative study with other odontogenic cysts.SPARC 在牙源性角化囊肿中的免疫组织化学表达:与其他牙源性囊肿的比较研究。
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Korean J Pathol. 2014 Jun;48(3):175-87. doi: 10.4132/KoreanJPathol.2014.48.3.175. Epub 2014 Jun 26.
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