MAGE-A1 promotes melanoma proliferation and migration through C-JUN activation
Copyright © 2016. Published by Elsevier Inc..
MAGE-A1 belongs to the chromosome X-clustered genes of cancer-testis antigen family and is normally expressed in the human germ line but is also overexpressed in various tumors. Previous studies of MAGE-A1 in melanoma mainly focused on methylation changes or its role in immunotherapy, however, its biological functions in melanoma have remained unknown. In order to determine the role of MAGE-A1 in melanoma growth and metastasis, we manipulated melanoma cell lines with overexpression and knockdown of MAGE-A1. Integration of cell proliferation assays, transwell migration and invasion assays, and RNA-Seq analysis revealed that up-regulation of MAGE-A1 dramatically promoted proliferation, migration, and invasion of human melanoma cell lines in vitro, while down-regulation of MAGE-A1 inhibited those characteristics associated with tumor cells. Furthermore, transcriptome sequencing revealed that MAGE-A1 exerts its tumor promoting activity by activating p-C-JUN directly or through ERK-MAPK signaling pathways. Based on our findings, we propose that MAGE-A1 may be a potential therapeutic target for melanoma patients.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2016 |
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| Erschienen: |
2016 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:473 |
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| Enthalten in: |
Biochemical and biophysical research communications - 473(2016), 4 vom: 13. Mai, Seite 959-965 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Wang, Dong [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Completed 13.06.2017 Date Revised 09.04.2022 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1016/j.bbrc.2016.03.161 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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NLM259080241 |
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| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Copyright © 2016. Published by Elsevier Inc. | ||
| 520 | |a MAGE-A1 belongs to the chromosome X-clustered genes of cancer-testis antigen family and is normally expressed in the human germ line but is also overexpressed in various tumors. Previous studies of MAGE-A1 in melanoma mainly focused on methylation changes or its role in immunotherapy, however, its biological functions in melanoma have remained unknown. In order to determine the role of MAGE-A1 in melanoma growth and metastasis, we manipulated melanoma cell lines with overexpression and knockdown of MAGE-A1. Integration of cell proliferation assays, transwell migration and invasion assays, and RNA-Seq analysis revealed that up-regulation of MAGE-A1 dramatically promoted proliferation, migration, and invasion of human melanoma cell lines in vitro, while down-regulation of MAGE-A1 inhibited those characteristics associated with tumor cells. Furthermore, transcriptome sequencing revealed that MAGE-A1 exerts its tumor promoting activity by activating p-C-JUN directly or through ERK-MAPK signaling pathways. Based on our findings, we propose that MAGE-A1 may be a potential therapeutic target for melanoma patients | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 4 | |a C-JUN | |
| 650 | 4 | |a ERK-MAPK | |
| 650 | 4 | |a MAGE-A1 | |
| 650 | 4 | |a RNA-seq | |
| 650 | 4 | |a Tumor metastasis | |
| 650 | 7 | |a MAGEA1 protein, human |2 NLM | |
| 650 | 7 | |a Melanoma-Specific Antigens |2 NLM | |
| 650 | 7 | |a Proto-Oncogene Proteins c-jun |2 NLM | |
| 650 | 7 | |a Extracellular Signal-Regulated MAP Kinases |2 NLM | |
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| 700 | 1 | |a Wang, Junyun |e verfasserin |4 aut | |
| 700 | 1 | |a Ding, Nan |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Yongjun |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Yaran |e verfasserin |4 aut | |
| 700 | 1 | |a Fang, Xiangdong |e verfasserin |4 aut | |
| 700 | 1 | |a Zhao, Hua |e verfasserin |4 aut | |
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