口腔鳞状细胞癌实质细胞和基质细胞中血管内皮生长因子和 iNOS 的共定位

A. Essa
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引用次数: 0

摘要

背景和目的:肿瘤血管生成和炎症感知与癌症进展有着错综复杂的联系。血管内皮生长因子(VEGF)与炎症细胞因子诱导型一氧化氮合酶(iNOS)在口腔鳞状细胞癌(OSCC)的实质细胞和基质细胞中的作用以及微血管密度(MVD)的评估中控制着不同病理条件下癌细胞代谢功能的血管生成过程。方法:免疫组化采用免疫组化方法分析 31 块石蜡切片中 VEGF、iNOS 和 CD31 的表达情况,这些石蜡切片分为 13 个分化良好、10 个中度分化和 8 个分化不良(石蜡切片 OSCC)。结果在所有等级的 OSCC 中,VEGF 和 iNOS 在实质细胞和基质细胞中均有较强的表达,同时 MVD 也有所增加。结论:VEGF 和 iNOS 的表达增强以及 MVD 可能与 OSCC 的分级有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Colocalization of VEGF and iNOS in Parenchymal and Stromal Cells of Oral Squamous Cell Carcinoma
Background and objectives: Tumor angiogenesis and inflammation perception are intricately linked to cancer progression. Vascular endothelial growth factor (VEGF) controls distinct procedures in angiogenesis of pathological conditions in metabolic functions of cancer cells with the inflammatory cytokine inducible nitric oxide synthase (iNOS) in parenchymal together with stromal cells of oral squamous cell carcinoma (OSCC) as well as assessing microvessel density (MVD). Methods: Immunohistochemistry was applied to analyze VEGF, iNOS as well as CD31 expression within 31 OSCCs paraffin blocks, which grouped into 13 well differentiated, 10 moderately differentiated, and 8 poorly differentiated (paraffin blocks OSCC). Results: Both VEGF and iNOS exhibit strong expression in both parenchymal and stromal cells in all grades of OSCC together with increased MVD. Conclusion: Enhanced expression of VEGF and iNOS together with MVD potentially correlate with OSCC grades.
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