Munne Pauliina M, Gu Yuexi, Tumiati Manuela, Gao Ping, Koopal Sonja, Uusivirta Sanna, Sawicki Janet, Wei Gong-Hong, Kuznetsov Sergey G
Institute for Molecular Medicine Finland (FIMM), University of Helsinki, PO Box 20, FIN-00014, Helsinki, Finland.
Biocenter Oulu and Department of Medical Biochemistry and Molecular Biology, Faculty of Biochemistry and Molecular Medicine, University of Oulu, P.O. Box 5000, Oulu FIN-90014, Finland.
Sci Rep. 2014 Apr 11;4:4663. doi: 10.1038/srep04663.
Multiple observations suggest a cell type-specific role for TP53 in mammary epithelia. We developed an in vitro assay, in which primary mouse mammary epithelial cells (mMECs) progressed from lumenal to basal-like phenotypes based on expression of Krt18 or ΔNp63, respectively. Such transition was markedly delayed in Trp53(-/-) mMECs suggesting that Trp53 is required for specification of the basal, but not lumenal cells. Evidence from human basal-like cell lines suggests that TP53 may support the activity of ΔNp63 by preventing its translocation from nucleoplasm into nucleoli. In human lumenal cells, activation of TP53 by inhibiting MDM2 or BRCA1 restored the nucleoplasmic expression of ΔNp63. Trp53(-/-) mMECs eventually lost epithelial features resulting in upregulation of MDM2 and translocation of ΔNp63 into nucleoli. We propose that TP63 may contribute to TP53-mediated oncogenic transformation of epithelial cells and shed light on tissue- and cell type-specific biases observed for TP53-related cancers.
多项观察结果表明,TP53在乳腺上皮细胞中具有细胞类型特异性作用。我们开发了一种体外检测方法,在该方法中,原代小鼠乳腺上皮细胞(mMECs)分别根据Krt18或ΔNp63的表达从管腔型转变为基底样表型。这种转变在Trp53(-/-) mMECs中明显延迟,这表明Trp53是基底细胞而非管腔细胞特化所必需的。来自人类基底样细胞系的证据表明,TP53可能通过阻止ΔNp63从核质转运到核仁来支持其活性。在人类管腔细胞中,通过抑制MDM2或BRCA1激活TP53可恢复ΔNp63的核质表达。Trp53(-/-) mMECs最终失去上皮特征,导致MDM2上调和ΔNp63转运到核仁。我们提出,TP63可能有助于TP53介导的上皮细胞致癌转化,并揭示了TP53相关癌症中观察到的组织和细胞类型特异性偏差。