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- W2743305788 abstract "Abstract Mounting evidence indicates that hotspot p53 mutant proteins often possess gain-of-function property in promoting cell mobility and tumor metastasis. However, the molecular mechanisms are not totally understood. In this study, we demonstrate that the hotspot mutation, p53-R273H, promotes cell migration, invasion in vitro and tumor metastasis in vivo . p53-R273H significantly represses expression of DLX2, a homeobox protein involved in cell proliferation and pattern formation. We show that p53-R273H-mediated DLX2 repression leads to upregulation of Neuropilin-2 (NRP2), a multifunctional co-receptor involved in tumor initiation, growth, survival and metastasis. p53-R273H-induced cell mobility is effectively suppressed by DLX2 expression. Furthermore, knockdown of NRP2 significantly inhibits p53-R273H-induced tumor metastasis in xenograft mouse model. Together, these results reveal an important role for DLX2-NRP2 in p53-R273H-induced cell mobility and tumor metastasis." @default.
- W2743305788 created "2017-08-17" @default.
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- W2743305788 date "2017-08-10" @default.
- W2743305788 modified "2023-10-06" @default.
- W2743305788 title "p53-R273H upregulates neuropilin-2 to promote cell mobility and tumor metastasis" @default.
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- W2743305788 doi "https://doi.org/10.1038/cddis.2017.376" @default.
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