Cancer Genomics Group, International Centre for Genetic Engineering and Biotechnology, Cape Town 7925, South Africa.
Division of Chemical and Systems Biology, Department of Integrative Biomedical Sciences, University of Cape Town, Cape Town 7925, South Africa.
Cells. 2023 Jul 31;12(15):1973. doi: 10.3390/cells12151973.
Defective in cullin neddylation 1 domain containing 1 (DCUN1D1) is an E3 ligase for the neddylation, a post-translational process similar to and occurring in parallel to ubiquitin proteasome pathway. Although established as an oncogene in a variety of squamous cell carcinomas, the precise role of DCUN1D1 in prostate cancer (PCa) has not been previously explored thoroughly. Here, we investigated the role of DCUN1D1 in PCa and demonstrated that DCUN1D1 is upregulated in cell lines as well as human tissue samples. Inhibition of DCUN1D1 significantly reduced PCa cell proliferation and migration and remarkably inhibited xenograft formation in mice. Applying both genomics and proteomics approaches, we provide novel information about the DCUN1D1 mechanism of action. We identified CUL3, CUL4B, RBX1, CAND1 and RPS19 proteins as DCUN1D1 binding partners. Our analysis also revealed the dysregulation of genes associated with cellular growth and proliferation, developmental, cell death and cancer pathways and the WNT/β-catenin pathway as potential mechanisms. Inhibition of DCUN1D1 leads to the inactivation of β-catenin through its phosphorylation and degradation which inhibits the downstream action of β-catenin, reducing its interaction with Lef1 in the Lef1/TCF complex that regulates Wnt target gene expression. Together our data point to an essential role of the DCUN1D1 protein in PCa which can be explored for potential targeted therapy.
缺乏环指蛋白 1 样结构域 1(DCUN1D1)是一种 neddylation 的 E3 连接酶,neddylation 是一种翻译后修饰过程,与泛素蛋白酶体途径相似且平行发生。虽然在多种鳞状细胞癌中已被确定为癌基因,但 DCUN1D1 在前列腺癌(PCa)中的确切作用尚未被充分探索。在这里,我们研究了 DCUN1D1 在 PCa 中的作用,并证明 DCUN1D1 在细胞系以及人类组织样本中均上调。抑制 DCUN1D1 可显著降低 PCa 细胞的增殖和迁移,并显著抑制小鼠异种移植的形成。通过应用基因组学和蛋白质组学方法,我们提供了关于 DCUN1D1 作用机制的新信息。我们确定了 CUL3、CUL4B、RBX1、CAND1 和 RPS19 蛋白作为 DCUN1D1 的结合伴侣。我们的分析还揭示了与细胞生长和增殖、发育、细胞死亡和癌症途径以及 WNT/β-catenin 途径相关的基因失调,这些途径可能是潜在的机制。抑制 DCUN1D1 会导致 β-catenin 磷酸化和降解,从而使其失活,从而抑制β-catenin 的下游作用,减少其与 Lef1/TCF 复合物中调节 Wnt 靶基因表达的 Lef1 的相互作用。综上所述,我们的数据表明 DCUN1D1 蛋白在 PCa 中起着至关重要的作用,可用于探索潜在的靶向治疗。