Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells

被引:1727
作者
Al-Nedawi, Khalid [1 ]
Meehan, Brian [1 ]
Micallef, Johann [3 ]
Lhotak, Vladimir [2 ]
May, Linda [2 ]
Guha, Abhijit [3 ]
Rak, Janusz [1 ]
机构
[1] McGill Univ, Montreal Childrens Hosp, Res Inst, Montreal, PQ H3Z 2Z3, Canada
[2] McMaster Univ, Henderson Res Ctr, Hamilton, ON L8V 1C3, Canada
[3] Univ Toronto, Hosp Sick Children, Arthur & Sonia Labatts Brain Tumor Ctr, Toronto, ON M5G 1L7, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1038/ncb1725
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
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(1). 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.
引用
收藏
页码:619 / U24
页数:16
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