Cironi Luisa, Riggi Nicolò, Provero Paolo, Wolf Natalie, Suvà Mario-Luca, Suvà Domizio, Kindler Vincent, Stamenkovic Ivan
Division of Experimental Pathology, Institute of Pathology CHUV, University of Lausanne, Lausanne, Switzerland.
PLoS One. 2008 Jul 9;3(7):e2634. doi: 10.1371/journal.pone.0002634.
The EWS-FLI-1 fusion protein is associated with 85-90% of Ewing's sarcoma family tumors (ESFT), the remaining 10-15% of cases expressing chimeric genes encoding EWS or FUS fused to one of several ets transcription factor family members, including ERG-1, FEV, ETV1 and ETV6. ESFT are dependent on insulin-like growth factor-1 (IGF-1) for growth and survival and recent evidence suggests that mesenchymal progenitor/stem cells constitute a candidate ESFT origin.
METHODOLOGY/PRINCIPAL FINDINGS: To address the functional relatedness between ESFT-associated fusion proteins, we compared mouse progenitor cell (MPC) permissiveness for EWS-FLI-1, EWS-ERG and FUS-ERG expression and assessed the corresponding expression profile changes. Whereas all MPC isolates tested could stably express EWS-FLI-1, only some sustained stable EWS-ERG expression and none could express FUS-ERG for more than 3-5 days. Only 14% and 4% of the total number of genes that were respectively induced and repressed in MPCs by the three fusion proteins were shared. However, all three fusion proteins, but neither FLI-1 nor ERG-1 alone, activated the IGF1 promoter and induced IGF1 expression.
CONCLUSION/SIGNIFICANCE: Whereas expression of different ESFT-associated fusion proteins may require distinct cellular microenvironments and induce transcriptome changes of limited similarity, IGF1 induction may provide one common mechanism for their implication in ESFT pathogenesis.
EWS-FLI-1融合蛋白与85%-90%的尤因肉瘤家族肿瘤(ESFT)相关,其余10%-15%的病例表达编码EWS或FUS与几种ets转录因子家族成员之一融合的嵌合基因,包括ERG-1、FEV、ETV1和ETV6。ESFT的生长和存活依赖胰岛素样生长因子-1(IGF-1),最近的证据表明间充质祖细胞/干细胞是ESFT的一个可能起源。
方法/主要发现:为了研究ESFT相关融合蛋白之间的功能相关性,我们比较了小鼠祖细胞(MPC)对EWS-FLI-1、EWS-ERG和FUS-ERG表达的允许性,并评估了相应的表达谱变化。虽然所有测试的MPC分离株都能稳定表达EWS-FLI-1,但只有一些能持续稳定表达EWS-ERG,没有一个能表达FUS-ERG超过3-5天。三种融合蛋白分别在MPC中诱导和抑制的基因总数中,只有14%和4%是相同的。然而,所有三种融合蛋白,而不是单独的FLI-1或ERG-1,都激活了IGF1启动子并诱导IGF1表达。
结论/意义:虽然不同的ESFT相关融合蛋白的表达可能需要不同的细胞微环境,并诱导有限相似性的转录组变化,但IGF1的诱导可能为它们参与ESFT发病机制提供一种共同机制。