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骨纤维异常增殖症、中央巨细胞肉芽肿和巨细胞瘤中c-Src的表达及细胞学特征比较

Expression of c-Src and comparison of cytologic features in cherubism, central giant cell granuloma and giant cell tumors.

作者信息

Wang Changning, Song Yaling, Peng Bin, Fan Mingwen, Li Jiang, Zhu Shengrong, Bian Zhuan

机构信息

Key Laboratory of Oral Biomedical Engineering, Ministry of Education of China, Wuhan University, Wuhan 430079, P.R. China.

出版信息

Oncol Rep. 2006 Mar;15(3):589-94.

Abstract

Cherubism (CBM) and central giant cell granuloma (CGCG) of the jaw and giant cell tumor (GCT) of the long bone are clinically different diseases. Histologically, they are all multinucleated giant cell (MGC)-containing lesions. This study aims to evaluate the expression of c-Src and cytologic features in CBM, CGCG and GCT and to clarify whether there is a common mechanism underlying the formation of multi-nucleated giant cells (MGCs) in these lesions. Specimens and paraffin blocks were collected from patients with CBM (12 cases), CGCG (24 cases) and GCT (37 cases). Histomorpho-metric differences in MGCs were compared among the three types of lesions. The expression of c-Src by immunohistochemistry and in situ hybridization and the expression of TRAP by enzyme histochemical staining were examined. Expression of c-Src mRNA and protein, as well as TRAP staining, was detected in both MGCs and a fraction of mononuclear cells in all investigated lesions. There are no quantitative differences for cytologic features and c-Src expression among the lesions. The results suggested that CBM, CGCG and GCT have overlapping cytological features at the histological level, and c-Src may be involved in the formation of MGCs in the three different diseases.

摘要

颌骨的 cherubism(CBM)、中央巨细胞肉芽肿(CGCG)以及长骨的巨细胞瘤(GCT)在临床上是不同的疾病。从组织学角度来看,它们均为含有多核巨细胞(MGC)的病变。本研究旨在评估 CBM、CGCG 和 GCT 中 c-Src 的表达及细胞学特征,以阐明这些病变中多核巨细胞(MGCs)形成的潜在共同机制。收集了 CBM 患者(12 例)、CGCG 患者(24 例)和 GCT 患者(37 例)的标本及石蜡块。比较了三种病变类型中 MGCs 的组织形态计量学差异。通过免疫组织化学和原位杂交检测 c-Src 的表达,通过酶组织化学染色检测 TRAP 的表达。在所有研究病变的 MGCs 和一部分单核细胞中均检测到了 c-Src mRNA 和蛋白的表达以及 TRAP 染色。病变之间在细胞学特征和 c-Src 表达方面没有定量差异。结果表明,CBM、CGCG 和 GCT 在组织学水平上具有重叠的细胞学特征,并且 c-Src 可能参与了这三种不同疾病中 MGCs 的形成。

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