Department of Morphofunctional Sciences I-Histology, Pathology, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Department of Pathology, Institute of Legal Medicine, Iasi, Romania.
Biomed Res Int. 2017;2017:8701386. doi: 10.1155/2017/8701386. Epub 2017 Dec 25.
Periostin (PN) epithelial and stromal overexpression in tumor pathology has been studied according to tumor growth, angiogenesis, invasiveness, and metastasis, but a limited number of studies address PN in thyroid tumors.
Our study aimed to analyze PN expression in different histological variants of PTC and to correlate its expression with the clinicopathological prognostic factors.
PN expression has been immunohistochemically assessed in 50 cases of PTC (conventional, follicular, oncocytic, macrofollicular, and tall cell variants), in tumor epithelial cells and intratumoral stroma. The association between PN expression and clinicopathological characteristics has been evaluated.
Our results show that PTC presented different patterns of PN immunoreaction, stromal PN being significantly associated with advanced tumor stage and extrathyroidal extension. No correlations were found between PN overexpression in tumor epithelial cells and clinicopathological features, except for specific histological variants, the highest risk of poor outcome being registered for the conventional subtype in comparison to the oncocytic type.
Our study demonstrates differences in PN expression in histological subtypes of PTC. Our results plead in favor of a dominant protumorigenic role of stromal PN, while the action of epithelial PN is less noticeable.
已有研究表明,在肿瘤病理学中,骨膜蛋白(periostin,PN)在肿瘤上皮细胞和基质中的过度表达与肿瘤的生长、血管生成、侵袭和转移有关,但关于甲状腺肿瘤中 PN 的研究数量有限。
本研究旨在分析不同组织学类型的甲状腺癌(papillary thyroid carcinoma,PTC)中 PN 的表达,并探讨其表达与临床病理预后因素的关系。
采用免疫组织化学方法检测 50 例 PTC(普通型、滤泡型、嗜酸细胞型、巨滤泡型和高细胞型)中 PN 的表达,检测肿瘤上皮细胞和肿瘤间质中 PN 的表达。评估 PN 表达与临床病理特征的关系。
本研究结果显示,PTC 呈现出不同的 PN 免疫反应模式,间质 PN 与晚期肿瘤分期和甲状腺外侵犯显著相关。肿瘤上皮细胞中 PN 的过度表达与临床病理特征之间无相关性,但在特定的组织学类型中除外,与嗜酸细胞型相比,普通型的不良预后风险最高。
本研究表明,PTC 的组织学亚型中存在 PN 表达的差异。我们的研究结果表明,基质 PN 具有明显的促肿瘤作用,而上皮 PN 的作用则不明显。