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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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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