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Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma
Due to the poor prognosis of advanced metastatic melanoma, it is crucial to find early biomarkers that help identify which melanomas will metastasize. By comparing the gene expression data from primary and cutaneous melanoma samples from The Cancer Genome Atlas (TCGA), we identified GPC6 among a set...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568403/ https://www.ncbi.nlm.nih.gov/pubmed/31199813 http://dx.doi.org/10.1371/journal.pone.0218067 |
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author | Li, Yuanyuan Li, Melissa Shats, Igor Krahn, Juno M. Flake, Gordon P. Umbach, David M. Li, Xiaoling Li, Leping |
author_facet | Li, Yuanyuan Li, Melissa Shats, Igor Krahn, Juno M. Flake, Gordon P. Umbach, David M. Li, Xiaoling Li, Leping |
author_sort | Li, Yuanyuan |
collection | PubMed |
description | Due to the poor prognosis of advanced metastatic melanoma, it is crucial to find early biomarkers that help identify which melanomas will metastasize. By comparing the gene expression data from primary and cutaneous melanoma samples from The Cancer Genome Atlas (TCGA), we identified GPC6 among a set of genes whose expression levels can distinguish between primary melanoma and regional cutaneous/subcutaneous metastases. Glypicans are thought to play a role in tumor growth by regulating the signaling pathways of Wnt, Hedgehogs, fibroblast growth factors (FGFs), and bone morphogenetic proteins (BMPs). We showed that GPC6 expression was up-regulated in a melanoma cell line compared to normal melanocytes and in metastatic melanoma compared to primary melanoma. Furthermore, GPC6 expression was positively correlated with genes largely involved in cell adhesion and migration in both melanoma samples and in RNA-seq samples from other TCGA tumors. Our results suggest that GPC6 may play a role in tumor metastatic progression. In TCGA melanoma samples, we also showed that GPC6 expression was negatively correlated with miR-509-3p, which has previously been shown to function as a tumor suppressor in various cancer cell lines. We overexpressed miR-509-3p in A375 melanoma cells and showed that GPC6 expression was significantly suppressed. This result suggested that GPC6 was a putative target of miR-509-3p in melanoma. Together, our findings identified GPC6 as an early biomarker for melanoma metastatic progression, one that can be regulated by miR-509-3p. |
format | Online Article Text |
id | pubmed-6568403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65684032019-06-20 Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma Li, Yuanyuan Li, Melissa Shats, Igor Krahn, Juno M. Flake, Gordon P. Umbach, David M. Li, Xiaoling Li, Leping PLoS One Research Article Due to the poor prognosis of advanced metastatic melanoma, it is crucial to find early biomarkers that help identify which melanomas will metastasize. By comparing the gene expression data from primary and cutaneous melanoma samples from The Cancer Genome Atlas (TCGA), we identified GPC6 among a set of genes whose expression levels can distinguish between primary melanoma and regional cutaneous/subcutaneous metastases. Glypicans are thought to play a role in tumor growth by regulating the signaling pathways of Wnt, Hedgehogs, fibroblast growth factors (FGFs), and bone morphogenetic proteins (BMPs). We showed that GPC6 expression was up-regulated in a melanoma cell line compared to normal melanocytes and in metastatic melanoma compared to primary melanoma. Furthermore, GPC6 expression was positively correlated with genes largely involved in cell adhesion and migration in both melanoma samples and in RNA-seq samples from other TCGA tumors. Our results suggest that GPC6 may play a role in tumor metastatic progression. In TCGA melanoma samples, we also showed that GPC6 expression was negatively correlated with miR-509-3p, which has previously been shown to function as a tumor suppressor in various cancer cell lines. We overexpressed miR-509-3p in A375 melanoma cells and showed that GPC6 expression was significantly suppressed. This result suggested that GPC6 was a putative target of miR-509-3p in melanoma. Together, our findings identified GPC6 as an early biomarker for melanoma metastatic progression, one that can be regulated by miR-509-3p. Public Library of Science 2019-06-14 /pmc/articles/PMC6568403/ /pubmed/31199813 http://dx.doi.org/10.1371/journal.pone.0218067 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Li, Yuanyuan Li, Melissa Shats, Igor Krahn, Juno M. Flake, Gordon P. Umbach, David M. Li, Xiaoling Li, Leping Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
title | Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
title_full | Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
title_fullStr | Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
title_full_unstemmed | Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
title_short | Glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
title_sort | glypican 6 is a putative biomarker for metastatic progression of cutaneous melanoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568403/ https://www.ncbi.nlm.nih.gov/pubmed/31199813 http://dx.doi.org/10.1371/journal.pone.0218067 |
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