Stuart E T, Kioussi C, Aguzzi A, Gruss P
Department of Molecular Cell Biology, Max-Planck Institute for Biophysical Chemistry, Am Fassberg, 37077 Göttingen, Germany.
Clin Cancer Res. 1995 Feb;1(2):207-14.
Rearrangements concerning chromosome 9p are a late event in the progression of human astrocytic tumors to their most malignant form. The expression of PAX5, which maps to chromosome 9p13, was studied in primary human brain tumors of astrocytic origin. Whereas murine Pax5 is not expressed in the forebrain at any stage, PAX5 expression was increased in a range of astrocytomas (WHO grades II-IV) which originated in the forebrain. Expression of PAX5 was limited to those cells which also expressed the oncogenes myc, fos, or jun singularly or in combination. The epidermal growth factor receptor was highly expressed in glioblastoma multiform tumors in areas which were also highly PAX5 positive. We conclude that the missappropriate expression of PAX5 may aid in promoting the progression of astrocytomal malignancy.
与9号染色体短臂相关的重排是人类星形细胞瘤发展至最恶性形式过程中的晚期事件。对定位于9号染色体短臂13区的PAX5在人原发性星形细胞源性脑肿瘤中的表达进行了研究。虽然小鼠Pax5在任何阶段的前脑中均不表达,但在一系列起源于前脑的星形细胞瘤(世界卫生组织分级II - IV级)中PAX5表达增加。PAX5的表达仅限于那些单独或联合表达癌基因myc、fos或jun的细胞。表皮生长因子受体在多形性胶质母细胞瘤中PAX5也呈高阳性的区域高度表达。我们得出结论,PAX5的异常表达可能有助于促进星形细胞瘤恶性程度的进展。