AI Article Synopsis
- GLIPR1 is frequently downregulated in prostate cancer, and this downregulation is associated with increased levels of c-Myc, a factor promoting cancer growth.
- Restoration of GLIPR1 expression leads to decreased c-Myc levels, inhibiting cancer cell progression by disrupting a specific signaling pathway that typically enhances c-Myc production.
- The study highlights the role of GLIPR1 in regulating c-Myc degradation through mechanisms involving phosphorylation and the movement of signaling proteins, suggesting that GLIPR1 plays a critical role in preventing prostate cancer development.
Article Abstract
Downregulation of the proapoptotic p53 target gene glioma pathogenesis-related protein 1 (GLIPR1) occurs frequently in prostate cancer, but the functional meaning of this event is obscure. Here, we report the discovery of functional relationship between GLIPR1 and c-Myc in prostate cancer where c-Myc is often upregulated. We found that the expression of GLIPR1 and c-Myc were inversely correlated in human prostate cancer. Restoration of GLIPR1 expression in prostate cancer cells downregulated c-myc levels, inhibiting cell-cycle progression. Downregulation was linked to a reduction in β-catenin/TCF4-mediated transcription of the c-myc gene, which was caused by GLIPR1-mediated redistribution of casein kinase 1α (CK1α) from the Golgi apparatus to the cytoplasm where CK1α could phosphorylate β-catenin and mediate its destruction. In parallel, GLIPR1 also promoted c-Myc protein ubiquitination and degradation by glycogen synthase kinase-3α- and/or CK1α-mediated c-Myc phosphorylation. Notably, genetic ablation of the mouse homolog of Glipr1 cooperated with c-myc overexpression to induce prostatic intraepithelial neoplasia and prostate cancer. Together, our findings provide evidence for CK1α-mediated destruction of c-Myc and identify c-Myc S252 as a crucial CK1α phosphorylation site for c-Myc degradation. Furthermore, they reveal parallel mechanisms of c-myc downregulation by GLIPR1 that when ablated in the prostate are sufficient to drive c-Myc expression and malignant development.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813470 | PMC |
| http://dx.doi.org/10.1158/0008-5472.CAN-11-1714 | DOI Listing |
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