American Association for Cancer Research
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Supplementary Fig S2 from miR-154* and miR-379 in the DLK1-DIO3 MicroRNA Mega-Cluster Regulate Epithelial to Mesenchymal Transition and Bone Metastasis of Prostate Cancer

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posted on 2023-03-31, 18:28 authored by Murali Gururajan, Sajni Josson, Gina Chia-Yi Chu, Chia-Lun Lu, Yi-Tsung Lu, Christopher L. Haga, Haiyen E. Zhau, Chunyan Liu, Jake Lichterman, Peng Duan, Edwin M. Posadas, Leland W.K. Chung

Supplementary Fig S2. (A) Expression of miR-409-3p and miR-154* assayed by qRT- PCR in ARCaPM-C control PCa cells and ARCaPM-cluster inhibitor transduced cells. Data is normalized to RNU6B. (B) Morphological changes in ARCaPM-cluster inhibitor compared to ARCaPM-C control PCa cells. (C) E-cadherin and N-cadherin mRNA assayed in ARCaPM-C control PCa cells and ARCaPM cluster inhibitor expressing PCa cells by qRT-PCR, normalized to 18s RNA. (D) Invasion assay of in ARCaPM-C and ARCaPM-cluster inhibitor expressing PCa cells. *: p<0.05 was considered to be statistically significant by t-test.



Purpose: MicroRNAs in the delta-like 1 homolog–deiodinase, iodothyronine 3 (DLK1-DIO3) cluster have been shown to be critical for embryonic development and epithelial to mesenchymal transition (EMT). DLK1-DIO3 cluster miRNAs are elevated in the serum of patients with metastatic cancer. However, the biologic functions of these miRNAs in the EMT and metastasis of cancer cells are poorly understood. We previously demonstrated the oncogenic and metastatic role of miR-409-3p/5p, a member of this cluster, in prostate cancer. In this study, we defined the role of miR-154* and miR-379, two key members of this cluster, in prostate cancer progression and bone metastasis in both cell line models and clinical specimens.Experimental Design: Genetic manipulation of miR-154* and miR-379 was performed to determine their role in tumor growth, EMT, and bone metastasis in mouse models. We determined the expression of miR-154* in prostate cancer clinical samples and bone metastasis samples using in situ hybridization and quantum dot labeling.Results: Elevated expression of miR-154* and miR-379 was observed in bone metastatic prostate cancer cell lines and tissues, and miR-379 expression correlated with progression-free survival of patients with prostate cancer. Intracardiac inoculation (to mimic systemic dissemination) of miR-154* inhibitor-treated bone metastatic ARCaPM prostate cancer cells in mice led to decreased bone metastasis and increased survival.Conclusion: miR-154* and miR-379 play important roles in prostate cancer biology by facilitating tumor growth, EMT, and bone metastasis. This finding has particular translational importance because miRNAs in the DLK1-DIO3 cluster can be attractive biomarkers and possible therapeutic targets to treat bone metastatic prostate cancer. Clin Cancer Res; 20(24); 6559–69. ©2014 AACR.