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Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1.

Authors :
Juneja M
Kobelt D
Walther W
Voss C
Smith J
Specker E
Neuenschwander M
Gohlke BO
Dahlmann M
Radetzki S
Preissner R
von Kries JP
Schlag PM
Stein U
Source :
PLoS biology [PLoS Biol] 2017 Jun 01; Vol. 15 (6), pp. e2000784. Date of Electronic Publication: 2017 Jun 01 (Print Publication: 2017).
Publication Year :
2017

Abstract

MACC1 (Metastasis Associated in Colon Cancer 1) is a key driver and prognostic biomarker for cancer progression and metastasis in a large variety of solid tumor types, particularly colorectal cancer (CRC). However, no MACC1 inhibitors have been identified yet. Therefore, we aimed to target MACC1 expression using a luciferase reporter-based high-throughput screening with the ChemBioNet library of more than 30,000 compounds. The small molecules lovastatin and rottlerin emerged as the most potent MACC1 transcriptional inhibitors. They remarkably inhibited MACC1 promoter activity and expression, resulting in reduced cell motility. Lovastatin impaired the binding of the transcription factors c-Jun and Sp1 to the MACC1 promoter, thereby inhibiting MACC1 transcription. Most importantly, in CRC-xenografted mice, lovastatin and rottlerin restricted MACC1 expression and liver metastasis. This is-to the best of our knowledge-the first identification of inhibitors restricting cancer progression and metastasis via the novel target MACC1. This drug repositioning might be of therapeutic value for CRC patients.

Subjects

Subjects :
Acetophenones adverse effects
Acetophenones chemistry
Acetophenones pharmacology
Animals
Antineoplastic Agents adverse effects
Antineoplastic Agents chemistry
Antineoplastic Agents pharmacology
Benzopyrans adverse effects
Benzopyrans chemistry
Benzopyrans pharmacology
Binding Sites
Cell Line, Tumor
Cell Proliferation drug effects
Colorectal Neoplasms metabolism
Colorectal Neoplasms pathology
Female
Genes, Reporter drug effects
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors chemistry
Hydroxymethylglutaryl-CoA Reductase Inhibitors pharmacology
Liver Neoplasms, Experimental prevention & control
Liver Neoplasms, Experimental secondary
Mice, SCID
Molecular Docking Simulation
Neoplasm Proteins antagonists & inhibitors
Neoplasm Proteins chemistry
Neoplasm Proteins genetics
Neoplasm Proteins metabolism
Promoter Regions, Genetic drug effects
Random Allocation
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Small Molecule Libraries
Trans-Activators
Transcription Factors chemistry
Transcription Factors genetics
Transcription Factors metabolism
Tumor Burden drug effects
Uncoupling Agents adverse effects
Uncoupling Agents chemistry
Uncoupling Agents pharmacology
Xenograft Model Antitumor Assays
Acetophenones therapeutic use
Antineoplastic Agents therapeutic use
Benzopyrans therapeutic use
Colorectal Neoplasms drug therapy
Gene Expression Regulation, Neoplastic drug effects
Hydroxymethylglutaryl-CoA Reductase Inhibitors therapeutic use
Transcription Factors antagonists & inhibitors
Uncoupling Agents therapeutic use

Details

Language :
English
ISSN :
1545-7885
Volume :
15
Issue :
6
Database :
MEDLINE
Journal :
PLoS biology
Publication Type :
Academic Journal
Accession number :
28570591
Full Text :
https://doi.org/10.1371/journal.pbio.2000784