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获得一种致癌融合蛋白足以全面改变微小RNA(miRNA)表达格局,从而抑制肌源性分化。

Acquisition of an oncogenic fusion protein is sufficient to globally alter the landscape of miRNA expression to inhibit myogenic differentiation.

作者信息

Loupe Jacob M, Miller Patrick J, Crabtree Judy S, Zabaleta Jovanny, Hollenbach Andrew D

机构信息

Current/Present address: Center for Human Genetic Research, Massachusetts General Hospital, Richard B. Simches Research Center, Boston, MA 02114, USA.

Current/Present address: Tulane University, New Orleans, LA 70112, USA.

出版信息

Oncotarget. 2017 Jul 29;8(50):87054-87072. doi: 10.18632/oncotarget.19693. eCollection 2017 Oct 20.

Abstract

The differentiation status of tumors is used as a prognostic indicator, with tumors comprised of less differentiated cells exhibiting higher levels of aggressiveness that correlate with a poor prognosis. Although oncogenes contribute to blocking differentiation, it is not clear how they globally alter miRNA expression during differentiation to achieve this result. The pediatric sarcoma Alveolar Rhabdomyosarcoma, which is primarily characterized by the expression of the PAX3-FOXO1 oncogenic fusion protein, consists of undifferentiated muscle cells. However, it is unclear what role PAX3-FOXO1 plays in promoting the undifferentiated state. We demonstrate that expression of PAX3-FOXO1 globally alters the expression of over 80 individual miRNA during early myogenic differentiation, resulting in three primary effects: 1) inhibition of the expression of 51 miRNA essential for promoting myogenesis, 2) promoting the aberrant expression of 43 miRNA not normally expressed during myogenesis, and 3) altering the expression pattern of 39 additional miRNA. Combined, these changes are predicted to have an overall negative effect on myogenic differentiation. This is one of the first studies describing how an oncogene globally alters miRNA expression to block differentiation and has clinical implications for the development of much needed multi-faceted tumor-specific therapeutic regimens.

摘要

肿瘤的分化状态被用作一种预后指标,由分化程度较低的细胞组成的肿瘤表现出更高的侵袭性水平,这与不良预后相关。尽管癌基因有助于阻止分化,但尚不清楚它们在分化过程中如何全局改变miRNA表达以实现这一结果。小儿肉瘤肺泡横纹肌肉瘤主要以PAX3-FOXO1致癌融合蛋白的表达为特征,由未分化的肌肉细胞组成。然而,尚不清楚PAX3-FOXO1在促进未分化状态中起什么作用。我们证明,在早期肌源性分化过程中,PAX3-FOXO1的表达全局改变了80多个个体miRNA的表达,产生了三个主要影响:1)抑制51种对促进肌生成至关重要的miRNA的表达;2)促进43种在肌生成过程中通常不表达的miRNA的异常表达;3)改变另外39种miRNA的表达模式。综合起来,这些变化预计对肌源性分化产生总体负面影响。这是首批描述癌基因如何全局改变miRNA表达以阻止分化的研究之一,对开发急需的多方面肿瘤特异性治疗方案具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1e/5675615/4eca0e6c3c08/oncotarget-08-87054-g001.jpg

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