Literature DB >> 29074607

Targeting the lipid metabolic axis ACSL/SCD in colorectal cancer progression by therapeutic miRNAs: miR-19b-1 role.

Silvia Cruz-Gil1, Ruth Sanchez-Martinez2, Marta Gomez de Cedron1, Roberto Martin-Hernandez3, Teodoro Vargas1, Susana Molina1, Jesús Herranz4, Alberto Davalos5, Guillermo Reglero1, Ana Ramirez de Molina2.   

Abstract

An abnormal acyl-CoA synthetase/stearoyl-CoA desaturase (ACSL/SCD) lipid network fuels colon cancer progression, endowing cells with invasive and migratory properties. Therapies against this metabolic network may be useful to improve clinical outcomes. Because micro-RNAs (miRNAs/miRs) are important epigenetic regulators, we investigated novel miRNAs targeting this pro-tumorigenic axis; hence to be used as therapeutic or prognostic miRNAs. Thirty-one putative common miRNAs were predicted to simultaneously target the three enzymes comprising the ACSL/SCD network. Target validation by quantitative RT-PCR, Western blotting, and luciferase assays showed miR-544a, miR-142, and miR-19b-1 as major regulators of the metabolic axis, ACSL/SCD Importantly, lower miR-19b-1 expression was associated with a decreased survival rate in colorectal cancer (CRC) patients, accordingly with ACSL/SCD involvement in patient relapse. Finally, miR-19b-1 regulated the pro-tumorigenic axis, ACSL/SCD, being able to inhibit invasion in colon cancer cells. Because its expression correlated with an increased survival rate in CRC patients, we propose miR-19b-1 as a potential noninvasive biomarker of disease-free survival and a promising therapeutic miRNA in CRC.
Copyright © 2018 by the American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  acyl-CoA synthetase/stearoyl-CoA desaturase; clinical studies; colorectal tumors; fatty acid/metabolism; invasiveness; lipid and lipoprotein metabolism; micro-ribonucleic acid; molecular biology; patient relapse

Mesh:

Substances:

Year:  2017        PMID: 29074607      PMCID: PMC5748493          DOI: 10.1194/jlr.M076752

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


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