Shoshan Y, Nishiyama A, Chang A, Mörk S, Barnett G H, Cowell J K, Trapp B D, Staugaitis S M
Department of Neurosciences, The Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Proc Natl Acad Sci U S A. 1999 Aug 31;96(18):10361-6. doi: 10.1073/pnas.96.18.10361.
The early events in neoplastic transformation can be understood only by comparison of the neoplastic cell with its nontransformed counterpart. The most common central nervous system gliomas traditionally are thought to arise from mature astrocytes and oligodendrocytes. We examined the possibility that gliomas arise from a population of glia that has properties of oligodendrocyte progenitors. These glial cells express the NG2 chondroitin sulfate proteoglycan and the alpha receptor of platelet-derived growth factor in vivo. We identified NG2 and the alpha receptor of platelet-derived growth factor expression in tissue from seven of seven oligodendrogliomas, three of three pilocytic astrocytomas, and one of five glioblastoma multiforme. These data provide evidence that glial tumors arise from glial progenitor cells. Molecules expressed by these progenitor cells should be considered as targets for novel therapeutics.
只有通过将肿瘤细胞与其未转化的对应细胞进行比较,才能理解肿瘤转化的早期事件。传统上认为,最常见的中枢神经系统胶质瘤起源于成熟的星形胶质细胞和少突胶质细胞。我们研究了胶质瘤是否起源于具有少突胶质前体细胞特性的胶质细胞群体的可能性。这些胶质细胞在体内表达硫酸软骨素蛋白聚糖NG2和血小板衍生生长因子的α受体。我们在7例少突胶质细胞瘤、3例毛细胞型星形细胞瘤和5例多形性胶质母细胞瘤中的1例的组织中鉴定出了NG2和血小板衍生生长因子的α受体表达。这些数据提供了胶质肿瘤起源于胶质前体细胞的证据。这些前体细胞表达的分子应被视为新型治疗的靶点。