Downregulation of YAP-dependent Nupr1 promotes tumor-repopulating cell growth in soft matrices

作者：Jia, Q.; Zhou, W.; Yao, W.; Yang, F.; Zhang, S.; Singh, R.; Chen, J.; Chen, J. J.; Zhang, Y.; Wei, F.; Zhang, Y.; Jia, H.; Wang, N.^*

来源：Oncogenesis, 2016, 5(4): e220.

DOI：10.1038/oncsis.2016.29

• BREAST-CANCER CELLS
• STEM-CELLS
• CONTACT INHIBITION
• INITIATING CELLS
• HIPPO PATHWAY
• EMERGING ROLE
• SELF-RENEWAL
• SOX2
• EXPRESSION
• STRESS

Despite decades of significant progress in understanding the molecular mechanisms of malignant tumorigenic cells, it remains elusive what these tumorigenic cells are and what controls the growth of these malignant cells. Recently, we have mechanically selected and grown highly malignant and tumorigenic tumor-repopulating cells (TRCs), a small sub-population of cancer cells, by culturing single cancer cells in soft fibrin matrices. However, it is unclear what regulates TRC growth besides Sox2. Here we show that nuclear protein 1 (Nupr1), a protein independent of Sox2, is downregulated in TRCs of melanoma, ovarian cancer and breast cancer cultured in soft fibrin matrices. Nupr1 expression depends on nuclear translocation of YAP that is enriched at the Nupr1 promoter sites; YAP is controlled by Cdc42-mediated F-actin and Lats1 interactions. Nupr1 regulates tumor-suppressor p53 and negatively regulates Nestin and Tert that are independent of Sox2 and promote TRC growth. Silencing Nupr1 increases TRC growth and Nupr1 overexpression inhibits TRC growth in culture and in immune-competent mice. Our results suggest that Nupr1 is a suppressor of growth of highly tumorigenic TRCs and may have a critical role in cancer progression.

• 出版日期2016-4
• 单位华中科技大学