Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression

Although mounting evidence indicates the involvement of galectin-3 in cancer progression and metastasis, the underlying molecular mechanisms remain largely unknown. In this study, we investigated the effect and possible mechanism of galectin-3 on the migration and invasion of B16F10, a metastatic me...

Full description

Bibliographic Details
Main Authors: Wang, Yuan-Guo, Kim, Seok-Jun, Baek, Jung-Hwan, Lee, Hyun-Woo, Jeong, Seo-Young, Chun, Kyung-Hee
Format: Online
Language:English
Published: Korean Society for Biochemistry and Molecular Biology 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389077/
id pubmed-3389077
recordtype oai_dc
spelling pubmed-33890772012-07-11 Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression Wang, Yuan-Guo Kim, Seok-Jun Baek, Jung-Hwan Lee, Hyun-Woo Jeong, Seo-Young Chun, Kyung-Hee Original Article Although mounting evidence indicates the involvement of galectin-3 in cancer progression and metastasis, the underlying molecular mechanisms remain largely unknown. In this study, we investigated the effect and possible mechanism of galectin-3 on the migration and invasion of B16F10, a metastatic melanoma cell line, in which galectin-3 and matrix metalloproteinase-1 (MMP-1) were both found to be highly expressed. Knockdown of galectin-3 with specific siRNA reduced migration and invasion, which was associated with reduced expression of MMP-1. To further investigate the underlying mechanism, we examined the effect of galectin-3 knockdown on the activity of AP-1, a transcriptional factor regulating MMP-1 expression. We found that galectin-3 directly interacted with AP-1 and facilitated the binding of this complex to the MMP-1 promoter that drives MMP-1 transcription. Moreover, silencing of galectin-3 inhibited binding of fra-1 and c-Jun to promoter sites of MMP-1 gene. Consistent with these in vitro findings, our in vivo study demonstrated that galectin-3 shRNA treatment significantly reduced the total number of mouse lung metastatic nodules. Taken together, galectin-3 facilitates cell migration and invasion in melanoma in vitro and can induce metastasis in vivo, in part through, regulating the transcription activity of AP-1 and thereby up-regulating MMP-1 expression. Korean Society for Biochemistry and Molecular Biology 2012-06-30 2012-03-21 /pmc/articles/PMC3389077/ /pubmed/22437631 http://dx.doi.org/10.3858/emm.2012.44.6.044 Text en Copyright © 2012 by the Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Wang, Yuan-Guo
Kim, Seok-Jun
Baek, Jung-Hwan
Lee, Hyun-Woo
Jeong, Seo-Young
Chun, Kyung-Hee
spellingShingle Wang, Yuan-Guo
Kim, Seok-Jun
Baek, Jung-Hwan
Lee, Hyun-Woo
Jeong, Seo-Young
Chun, Kyung-Hee
Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
author_facet Wang, Yuan-Guo
Kim, Seok-Jun
Baek, Jung-Hwan
Lee, Hyun-Woo
Jeong, Seo-Young
Chun, Kyung-Hee
author_sort Wang, Yuan-Guo
title Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
title_short Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
title_full Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
title_fullStr Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
title_full_unstemmed Galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
title_sort galectin-3 increases the motility of mouse melanoma cells by regulating matrix metalloproteinase-1 expression
description Although mounting evidence indicates the involvement of galectin-3 in cancer progression and metastasis, the underlying molecular mechanisms remain largely unknown. In this study, we investigated the effect and possible mechanism of galectin-3 on the migration and invasion of B16F10, a metastatic melanoma cell line, in which galectin-3 and matrix metalloproteinase-1 (MMP-1) were both found to be highly expressed. Knockdown of galectin-3 with specific siRNA reduced migration and invasion, which was associated with reduced expression of MMP-1. To further investigate the underlying mechanism, we examined the effect of galectin-3 knockdown on the activity of AP-1, a transcriptional factor regulating MMP-1 expression. We found that galectin-3 directly interacted with AP-1 and facilitated the binding of this complex to the MMP-1 promoter that drives MMP-1 transcription. Moreover, silencing of galectin-3 inhibited binding of fra-1 and c-Jun to promoter sites of MMP-1 gene. Consistent with these in vitro findings, our in vivo study demonstrated that galectin-3 shRNA treatment significantly reduced the total number of mouse lung metastatic nodules. Taken together, galectin-3 facilitates cell migration and invasion in melanoma in vitro and can induce metastasis in vivo, in part through, regulating the transcription activity of AP-1 and thereby up-regulating MMP-1 expression.
publisher Korean Society for Biochemistry and Molecular Biology
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389077/
_version_ 1611540898328346624