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YKL-40由肿瘤细胞直接产生,在胶质母细胞瘤中与表皮生长因子受体呈负相关。

YKL-40 is directly produced by tumor cells and is inversely linked to EGFR in glioblastomas.

作者信息

Horbinski Craig, Wang Guoji, Wiley Clayton A

机构信息

Department of Pathology, Division of Neuropathology, University of Kentucky, 800 Rose Street, Lexington, KY 40536, USA.

出版信息

Int J Clin Exp Pathol. 2010 Jan 1;3(3):226-37.

Abstract

YKL-40 is a secreted chitinase-like molecule whose expression is associated with glioma grade. Expression is higher in astrocytomas than oligodendrogliomas and has been reported to predict shorter survival and radiation resistance in glioblastomas (GBMs). Whether YKL-40 is directly produced by glioma cells or other admixed nonneo-plastic cells, and whether it correlates with 1p/19q status or other hallmark molecular abnormalities, are unclear. A rank-order list of YKL-40 expression was determined immunohistochemically in 79 untreated high-grade adult glio-mas, including 28 anaplastic oligodendrogliomas (AOs) and 51 GBMs. Relative YKL-40 expression was compared with glioma class, key molecular alterations, and immunohistochemical markers via a series of Spearman rank correlations. YKL-40 mRNA in situ hybridization with colocalization assessment via confocal microscopy was also performed. YKL-40 mRNA was abundant in glioma cells as well as reactive astrocytes, but was low in admixed neurons and macrophages. YKL-40 expression was higher in GBMs than AOs (P < 0.0001) and among GBMs, YKL-40 expression was lower in tumors with either EGFR amplification (P = 0.005) or elevated EGFR expression (P = 0.001). Among AOs, no difference in YKL-40 expression was seen in tumors with 1p19q codeletion (P = 0.3), but loss of heterozygosity in 10q23 correlated with increased YKL-40 expression (P = 0.03). These data suggest that YKL-40 is predominantly expressed by neoplastic glial cells and is related to certain key molecular alterations.

摘要

YKL-40是一种分泌型几丁质酶样分子,其表达与胶质瘤分级相关。在星形细胞瘤中的表达高于少突胶质细胞瘤,并且据报道在胶质母细胞瘤(GBM)中可预测生存期较短和具有放射抗性。YKL-40是由胶质瘤细胞还是其他混合的非肿瘤细胞直接产生,以及它是否与1p/19q状态或其他标志性分子异常相关,目前尚不清楚。通过免疫组织化学方法确定了79例未经治疗的高级别成人胶质瘤(包括28例间变性少突胶质细胞瘤(AO)和51例GBM)中YKL-40表达的排序清单。通过一系列Spearman等级相关性分析,将YKL-40相对表达与胶质瘤类别、关键分子改变和免疫组织化学标志物进行了比较。还进行了YKL-40 mRNA原位杂交,并通过共聚焦显微镜进行了共定位评估。YKL-40 mRNA在胶质瘤细胞以及反应性星形胶质细胞中丰富,但在混合的神经元和巨噬细胞中含量较低。YKL-40在GBM中的表达高于AO(P<0.0001),并且在GBM中,YKL-40在伴有表皮生长因子受体(EGFR)扩增(P=0.005)或EGFR表达升高(P=0.001)的肿瘤中表达较低。在AO中,1p19q共缺失的肿瘤中YKL-40表达无差异(P=0.3),但10q23杂合性缺失与YKL-40表达增加相关(P=0.03)。这些数据表明YKL-40主要由肿瘤性胶质细胞表达,并与某些关键分子改变有关。

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