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题目:: The splicing factor SRSF1 regulates apoptosis and proliferation to promote mammary epithelial cell transformation.
作者:: Anczuków(Olga),Rosenberg(Avi Z),Akerman(Martin),Das(Shipra),Zhan(Lixing),Karni(Rotem),Muthuswamy(Senthil K),Krainer(Adrian R)
状态:: 发布时间2012-02-03 , 更新时间 2016-10-19
期刊:: Nat Struct Mol Biol
摘要:: The splicing-factor oncoprotein SRSF1 (also known as SF2/ASF or ASF/SF2) is upregulated in breast cancers. We investigated the ability of SRSF1 to transform human and mouse mammary epithelial cells in vivo and in vitro. SRSF1-overexpressing COMMA-1D cells formed tumors, following orthotopic transplantation to reconstitute the mammary gland. In three-dimensional (3D) culture, SRSF1-overexpressing MCF-10A cells formed larger acini than control cells, reflecting increased proliferation and delayed apoptosis during acinar morphogenesis. These effects required the first RNA-recognition motif and nuclear functions of SRSF1. SRSF1 overexpression promoted alternative splicing of BIM (also known as BCL2L11) and BIN1 to produce isoforms that lack pro-apoptotic functions and contribute to the phenotype. Finally, SRSF1 cooperated specifically with MYC to transform mammary epithelial cells, in part by potentiating eIF4E activation, and these cooperating oncogenes are significantly coexpressed in human breast tumors. Thus, SRSF1 can promote breast cancer, and SRSF1 itself or its downstream effectors may be valuable targets for the development of therapeutics.
语言:: eng
DOI:

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