Dickkopf-1 (DKK1) drives growth and metastases in castration-resistant prostate cancer

• Published in: Cancer gene therapy 2024-08, Vol.31 (8), p.1266-1279
• Main Authors: Rinella, Letizia, Fiorentino, Gloria, Compagno, Mara, Grange, Cristina, Cedrino, Massimo, Marano, Francesca, Bosco, Ornella, Vissio, Elena, Delsedime, Luisa, D’Amelio, Patrizia, Bussolati, Benedetta, Arvat, Emanuela, Catalano, Maria Graziella
• Format: Article
• Language: English
• Subjects: 13/2; 13/31; 13/44; 42/89; 45/77; 631/67; 631/67/589/466; 64/60; Biomedical and Life Sciences; Biomedicine; Cadherins; Castration; Cell cycle; Cell migration; Clonal deletion; CRISPR; Dkk1 protein; E-cadherin; Gene Expression; Gene Therapy; Localization; Lung cancer; Metastases; Metastasis; Prostate cancer; siRNA; Tubulin; Tumor cell lines; Tumors; Wnt protein; Xenografts; β-Catenin
• ISSN: 0929-1903; 1476-5500; 1476-5500
• DOI: 10.1038/s41417-024-00783-7

Metastatic castration-resistant prostate cancer (mCRPC) is associated with a poor prognosis and remains an incurable fatal disease. Therefore, the identification of molecular markers involved in cancer progression is urgently needed to develop more-effective therapies. The present study investigated the role of the Wnt signaling modulator Dickkopf-1 (DKK1) in the growth and metastatic progression of mCRPC. DKK1 silencing through siRNA and deletion via CRISPR/Cas9 editing were performed in two different metastatic castration-resistant prostate cancer cell lines (PC3 and DU145). A xenograft tumor model was used to assess tumor growth and metastases. In in vitro experiments, both DKK1 silencing and deletion reduced cell growth and migration of both cell lines. DKK1 knockout clones (DKK1-KO) exhibited cell cycle arrest, tubulin reorganization, and modulation of tumor metastasis-associated genes. Furthermore, in DKK1-KO cells, E-cadherin re-expression and its membrane co-localization with β-catenin were observed, contributing to reduced migration; Cadherin-11, known to increase during epithelial-mesenchymal transition, was down-regulated in DKK1-KO cells. In the xenograft mouse model, DKK1 deletion not only reduced tumor growth but also inhibited the formation of lung metastases. In conclusion, our findings support the key role of DKK1 in the growth and metastatic dissemination of mCRPC, both in vitro and in vivo.