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Histological study of chordoma origin from fetal notochordal cell rests

机译:胎儿脊索细胞休息区脊索瘤起源的组织学研究

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STUDY DESIGN.: The histological comparative study was performed on chordoma and notochordal cell rests (NCRs). OBJECTIVE.: To understand the histological similarity and homology of chordoma and NCRs, further supplying direct evidence of chordoma origin from NCRs. SUMMARY OF BACKGROUND DATA.: Although many studies supported the hypothesis that chordoma arise from NCRs, there has been little direct evidence reported to date. Of the base of our previous study, we conducted a comparative histological study among NCRs coexisting in chordoma, fetal NCRs, and chordoma tumor components. METHODS.: Thirty fetal nucleus pulposus and 46 chordoma specimens were harvested, and classic chordoma tumor markers and brachyury expression levels were investigated through immunohistochemical method. RESULTS.: The fetal NCRs existed in the form of clusters in the center of nucleus pulposus <36 gestational weeks; NCRs coexisting in chordoma specimens consisted of packed cells without extracellular myxoid matrix. Both the above-mentioned NCRs as well as chordoma tumor components showed high sensitivity for classic chordoma tumor makers (epithelial membrane antigen, AE1/AE3, CAM5.2, vimentin, S-100); both kinds of NCRs showed completely negative expression for brachyury, whereas chordoma tumor components demonstrated 100% positivity. CONCLUSION.: Our study results supported histological similarity and homology of NCRs coexisting in chordoma and in fetal nucleus pulposus. Brachyury activation probably takes an important role in chordoma tumoregenesis.
机译:研究设计:组织学比较研究在脊索瘤和脊索细胞休息(NCRs)。目的:了解脊索瘤和NCRs的组织学相似性和同源性,进一步为脊索瘤起源于NCRs提供直接证据。背景数据摘要:尽管许多研究支持脊索瘤起源于NCR的假说,但迄今为止,几乎没有直接的证据报道。在我们先前研究的基础上,我们在脊索瘤,胎儿NCR和脊索瘤肿瘤成分共存的NCR之间进行了比较组织学研究。方法:收集30例胎儿髓核和46例脊索瘤标本,并通过免疫组织化学方法研究经典脊索瘤的肿瘤标志物和腕膜上皮细胞的表达水平。结果:胎儿NCR以簇的形式存在于<36孕周的髓核中心。脊索瘤标本中共存的NCR由没有细胞外粘液样基质的堆积细胞组成。上述NCRs和脊索瘤肿瘤成分均显示出对经典脊索瘤肿瘤产生者(上皮膜抗原,AE1 / AE3,CAM5.2,波形蛋白,S-100)的高敏感性。两种NCR均显示出对短毛象的完全阴性表达,而脊索瘤的肿瘤成分则显示100%阳性。结论:我们的研究结果支持在脊索瘤和胎儿髓核中共存的NCRs的组织学相似性和同源性。布氏短视激活可能在脊索瘤的肿瘤发生中起重要作用。

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