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JUN癌基因扩增和过表达会阻碍高侵袭性肉瘤中的脂肪细胞分化。

JUN oncogene amplification and overexpression block adipocytic differentiation in highly aggressive sarcomas.

作者信息

Mariani Odette, Brennetot Caroline, Coindre Jean-Michel, Gruel Nadège, Ganem Carine, Delattre Olivier, Stern Marc-Henri, Aurias Alain

机构信息

Institut Curie, Genetics and Biology of Cancers, 26 rue d'Ulm, 75248 Paris cedex 05, France; INSERM U830, F-75005 Paris, France.

出版信息

Cancer Cell. 2007 Apr;11(4):361-74. doi: 10.1016/j.ccr.2007.02.007.

Abstract

The human oncogene JUN encodes a component of the AP-1 complex and is consequently involved in a wide range of pivotal cellular processes, including cell proliferation, transformation, and apoptosis. Nevertheless, despite extensive analyses of its functions, it has never been directly involved in a human cancer. We demonstrate here that it is highly amplified and overexpressed in undifferentiated and aggressive human sarcomas, which are blocked at an early step of adipocyte differentiation. We confirm by cellular and xenograft mouse models recapitulating these sarcoma genetics that the failure to differentiate is dependent upon JUN amplification/overexpression.

摘要

人类癌基因JUN编码AP-1复合物的一个组分,因此参与广泛的关键细胞过程,包括细胞增殖、转化和凋亡。然而,尽管对其功能进行了广泛分析,但它从未直接参与人类癌症。我们在此证明,它在未分化的侵袭性人类肉瘤中高度扩增并过表达,这些肉瘤在脂肪细胞分化的早期阶段受阻。我们通过重现这些肉瘤遗传学的细胞和异种移植小鼠模型证实,分化失败取决于JUN扩增/过表达。

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