Cargando…
Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1
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 exp...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453412/ https://www.ncbi.nlm.nih.gov/pubmed/28570591 http://dx.doi.org/10.1371/journal.pbio.2000784 |
_version_ | 1783240660037402624 |
---|---|
author | Juneja, Manisha Kobelt, Dennis Walther, Wolfgang Voss, Cynthia Smith, Janice Specker, Edgar Neuenschwander, Martin Gohlke, Björn-Oliver Dahlmann, Mathias Radetzki, Silke Preissner, Robert von Kries, Jens Peter Schlag, Peter Michael Stein, Ulrike |
author_facet | Juneja, Manisha Kobelt, Dennis Walther, Wolfgang Voss, Cynthia Smith, Janice Specker, Edgar Neuenschwander, Martin Gohlke, Björn-Oliver Dahlmann, Mathias Radetzki, Silke Preissner, Robert von Kries, Jens Peter Schlag, Peter Michael Stein, Ulrike |
author_sort | Juneja, Manisha |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5453412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54534122017-06-12 Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 Juneja, Manisha Kobelt, Dennis Walther, Wolfgang Voss, Cynthia Smith, Janice Specker, Edgar Neuenschwander, Martin Gohlke, Björn-Oliver Dahlmann, Mathias Radetzki, Silke Preissner, Robert von Kries, Jens Peter Schlag, Peter Michael Stein, Ulrike PLoS Biol Research Article 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. Public Library of Science 2017-06-01 /pmc/articles/PMC5453412/ /pubmed/28570591 http://dx.doi.org/10.1371/journal.pbio.2000784 Text en © 2017 Juneja et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Juneja, Manisha Kobelt, Dennis Walther, Wolfgang Voss, Cynthia Smith, Janice Specker, Edgar Neuenschwander, Martin Gohlke, Björn-Oliver Dahlmann, Mathias Radetzki, Silke Preissner, Robert von Kries, Jens Peter Schlag, Peter Michael Stein, Ulrike Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 |
title | Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 |
title_full | Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 |
title_fullStr | Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 |
title_full_unstemmed | Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 |
title_short | Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1 |
title_sort | statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via macc1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453412/ https://www.ncbi.nlm.nih.gov/pubmed/28570591 http://dx.doi.org/10.1371/journal.pbio.2000784 |
work_keys_str_mv | AT junejamanisha statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT kobeltdennis statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT waltherwolfgang statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT vosscynthia statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT smithjanice statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT speckeredgar statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT neuenschwandermartin statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT gohlkebjornoliver statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT dahlmannmathias statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT radetzkisilke statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT preissnerrobert statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT vonkriesjenspeter statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT schlagpetermichael statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 AT steinulrike statinandrottlerinsmallmoleculeinhibitorsrestrictcoloncancerprogressionandmetastasisviamacc1 |