Al-Nedawi Khalid, Meehan Brian, Micallef Johann, Lhotak Vladimir, May Linda, Guha Abhijit, Rak Janusz
Montreal Children's Hospital Research Institute, McGill University, 4060 Ste Catherine West, Montreal, Quebec, Canada H3Z 2Z3.
Nat Cell Biol. 2008 May;10(5):619-24. doi: 10.1038/ncb1725. Epub 2008 Apr 20.
Aggressive human brain tumours (gliomas) often express a truncated and oncogenic form of the epidermal growth factor receptor, known as EGFRvIII. Within each tumour only a small percentage of glioma cells may actually express EGFRvIII; however, most of the cells exhibit a transformed phenotype. Here we show that EGFRvIII can be 'shared' between glioma cells by intercellular transfer of membrane-derived microvesicles ('oncosomes'). EGFRvIII expression in indolent glioma cells stimulates formation of lipid-raft related microvesicles containing EGFRvIII. Microvesicles containing this receptor are then released to cellular surroundings and blood of tumour-bearing mice, and can merge with the plasma membranes of cancer cells lacking EGFRvIII. This event leads to the transfer of oncogenic activity, including activation of transforming signalling pathways (MAPK and Akt), changes in expression of EGFRvIII-regulated genes (VEGF, Bcl-x(L), p27), morphological transformation and increase in anchorage-independent growth capacity. Thus, membrane microvesicles of cancer cells can contribute to a horizontal propagation of oncogenes and their associated transforming phenotype among subsets of cancer cells.
侵袭性人脑肿瘤(胶质瘤)通常表达一种截短的、具有致癌性的表皮生长因子受体形式,即EGFRvIII。在每个肿瘤中,实际上只有一小部分胶质瘤细胞可能表达EGFRvIII;然而,大多数细胞呈现出转化表型。我们在此表明,EGFRvIII可通过膜衍生微泡(“肿瘤小体”)的细胞间转移在胶质瘤细胞之间“共享”。惰性胶质瘤细胞中EGFRvIII的表达刺激了含有EGFRvIII的脂筏相关微泡的形成。然后,含有该受体的微泡被释放到细胞周围环境和荷瘤小鼠的血液中,并可与缺乏EGFRvIII的癌细胞的质膜融合。这一事件导致致癌活性的转移,包括转化信号通路(MAPK和Akt)的激活、EGFRvIII调控基因(VEGF、Bcl-x(L)、p27)表达的变化、形态转化以及锚定非依赖性生长能力的增加。因此,癌细胞的膜微泡可促进癌基因及其相关转化表型在癌细胞亚群之间的水平传播。