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TIM-3 expression in human osteosarcoma: Correlation with the expression of epithelial-mesenchymal transition-specific biomarkers

机译:TIM-3在人骨肉瘤中的表达:与上皮-间质转化特异性生物标志物的表达相关

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摘要

Signals from the T cell Ig- and mucin-domain-containing molecules (TIMs) have been demonstrated to be actively involved in regulating the progression of carcinomas. However, the expression and distribution of these molecules in osteosarcoma, the most common primary bone malignancy with poor prognosis, have not been investigated. In this study, the expression of TIMs was examined in nine invasive human osteosarcomas using immunohistochemistry, and the phenotypes were detected by dual immunofluorescence staining. Using immunohistochemistry, it was observed that only TIM-3, rather than TIM-1 or TIM-4, was expressed in these tumor specimens, where it was localized in the cytoplasm and plasma membrane of tumor cells. Dual immunofluorescence staining revealed that the expression of TIM-3 was observed in all cell types investigated, including CD68+ macrophages, CD31+ endothelial cells, CK-18+ epithelial cells and PCNA+ tumor cells. Notably, in sarcoma cells, TIM-3 was co-expressed with certain biomarkers of epithelial-mesenchymal transition (EMT), including vimentin, Slug, Snail and Smad. These combined results suggest that TIM-3 triggers tumor cells to acquire features of aggressive EMT and may be involved in the pathogenesis of this malignancy.
机译:来自T细胞含Ig和粘蛋白域的分子(TIM)的信号已被证明积极参与调节癌症的进展。但是,尚未研究这些分子在骨肉瘤(最常见的原发性恶性肿瘤,预后不良)中的表达和分布。在这项研究中,使用免疫组织化学检查了TIMs在9种侵袭性人骨肉瘤中的表达,并通过双重免疫荧光染色检测了表型。使用免疫组织化学,观察到在这些肿瘤标本中仅表达TIM-3,而不表达TIM-1或TIM-4,其定位在肿瘤细胞的细胞质和质膜中。双重免疫荧光染色显示,在所有研究的细胞类型中均观察到TIM-3的表达,包括CD68 + 巨噬细胞,CD31 + 内皮细胞,CK-18 + 上皮细胞和PCNA + 肿瘤细胞。值得注意的是,在肉瘤细胞中,TIM-3与上皮-间质转化(EMT)的某些生物标记物共表达,包括波形蛋白,Slug,Snail和Smad。这些综合结果表明,TIM-3触发肿瘤细胞获得侵袭性EMT的特征,并可能参与了这种恶性肿瘤的发病机理。

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