S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction

The aberrant activity of Wnt signaling is an early step in the transformation of normal intestinal cells to malignant tissue, leading to more aggressive tumors, and eventually metastases. In colorectal cancer (CRC), metastasis accounts for about 90% of patient deaths, representing the most lethal ev...

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Main Authors: Mathias Dahlmann, Dennis Kobelt, Wolfgang Walther, Giridhar Mudduluru, Ulrike Stein
Format: Article
Language:English
Published: MDPI AG 2016-06-01
Series:Cancers
Subjects:
Online Access:http://www.mdpi.com/2072-6694/8/6/59
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spelling doaj-d8d13ec1bc3f4019bdd6f121f2a7f3332020-11-24T23:16:18ZengMDPI AGCancers2072-66942016-06-01865910.3390/cancers8060059cancers8060059S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis RestrictionMathias Dahlmann0Dennis Kobelt1Wolfgang Walther2Giridhar Mudduluru3Ulrike Stein4Experimental and Clinical Research Center, Charité University Medicine, Berlin and Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Str. 10, 13125 Berlin, GermanyExperimental and Clinical Research Center, Charité University Medicine, Berlin and Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Str. 10, 13125 Berlin, GermanyExperimental and Clinical Research Center, Charité University Medicine, Berlin and Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Str. 10, 13125 Berlin, GermanyExperimental and Clinical Research Center, Charité University Medicine, Berlin and Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Str. 10, 13125 Berlin, GermanyExperimental and Clinical Research Center, Charité University Medicine, Berlin and Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Str. 10, 13125 Berlin, GermanyThe aberrant activity of Wnt signaling is an early step in the transformation of normal intestinal cells to malignant tissue, leading to more aggressive tumors, and eventually metastases. In colorectal cancer (CRC), metastasis accounts for about 90% of patient deaths, representing the most lethal event during the course of the disease and is directly linked to patient survival, critically limiting successful therapy. This review focuses on our studies of the metastasis-inducing gene S100A4, which we identified as transcriptional target of β-catenin. S100A4 increased migration and invasion in vitro and metastasis in mice. In patient CRC samples, high S100A4 levels predict metastasis and reduced patient survival. Our results link pathways important for tumor progression and metastasis: the Wnt signaling pathway and S100A4, which regulates motility and invasiveness. S100A4 suppression by interdicting Wnt signaling has potential for therapeutic intervention. As proof of principle, we applied S100A4 shRNA systemically and prevented metastasis in mice. Furthermore, we identified small molecule inhibitors from high-throughput screens of pharmacologically active compounds employing an S100A4 promoter-driven reporter. Best hits act, as least in part, via intervening in the Wnt pathway and restricted metastasis in mouse models. We currently translate our findings on restricting S100A4-driven metastasis into clinical practice. The repositioned FDA-approved drug niclosamide, targeting Wnt signaling, is being tested in a prospective phase II clinical trial for treatment of CRC patients. Our assay for circulating S100A4 transcripts in patient blood is used to monitor treatment success.http://www.mdpi.com/2072-6694/8/6/59Wnt signalingcolorectal cancermetastasisS100A4intervention
collection DOAJ
language English
format Article
sources DOAJ
author Mathias Dahlmann
Dennis Kobelt
Wolfgang Walther
Giridhar Mudduluru
Ulrike Stein
spellingShingle Mathias Dahlmann
Dennis Kobelt
Wolfgang Walther
Giridhar Mudduluru
Ulrike Stein
S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction
Cancers
Wnt signaling
colorectal cancer
metastasis
S100A4
intervention
author_facet Mathias Dahlmann
Dennis Kobelt
Wolfgang Walther
Giridhar Mudduluru
Ulrike Stein
author_sort Mathias Dahlmann
title S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction
title_short S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction
title_full S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction
title_fullStr S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction
title_full_unstemmed S100A4 in Cancer Metastasis: Wnt Signaling-Driven Interventions for Metastasis Restriction
title_sort s100a4 in cancer metastasis: wnt signaling-driven interventions for metastasis restriction
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2016-06-01
description The aberrant activity of Wnt signaling is an early step in the transformation of normal intestinal cells to malignant tissue, leading to more aggressive tumors, and eventually metastases. In colorectal cancer (CRC), metastasis accounts for about 90% of patient deaths, representing the most lethal event during the course of the disease and is directly linked to patient survival, critically limiting successful therapy. This review focuses on our studies of the metastasis-inducing gene S100A4, which we identified as transcriptional target of β-catenin. S100A4 increased migration and invasion in vitro and metastasis in mice. In patient CRC samples, high S100A4 levels predict metastasis and reduced patient survival. Our results link pathways important for tumor progression and metastasis: the Wnt signaling pathway and S100A4, which regulates motility and invasiveness. S100A4 suppression by interdicting Wnt signaling has potential for therapeutic intervention. As proof of principle, we applied S100A4 shRNA systemically and prevented metastasis in mice. Furthermore, we identified small molecule inhibitors from high-throughput screens of pharmacologically active compounds employing an S100A4 promoter-driven reporter. Best hits act, as least in part, via intervening in the Wnt pathway and restricted metastasis in mouse models. We currently translate our findings on restricting S100A4-driven metastasis into clinical practice. The repositioned FDA-approved drug niclosamide, targeting Wnt signaling, is being tested in a prospective phase II clinical trial for treatment of CRC patients. Our assay for circulating S100A4 transcripts in patient blood is used to monitor treatment success.
topic Wnt signaling
colorectal cancer
metastasis
S100A4
intervention
url http://www.mdpi.com/2072-6694/8/6/59
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