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Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells
The tumor suppressor p53 functions by inducing the transcription of a collection of target genes. We previously attempted to identify p53 target genes by microarray expression and ChIP‐sequencing analyses. In this study, we describe a novel p53 target gene, FUCA1, which encodes a fucosidase. Althoug...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968591/ https://www.ncbi.nlm.nih.gov/pubmed/26998741 http://dx.doi.org/10.1111/cas.12933 |
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author | Ezawa, Issei Sawai, Yuichiro Kawase, Tatsuya Okabe, Atsushi Tsutsumi, Shuichi Ichikawa, Hitoshi Kobayashi, Yuka Tashiro, Fumio Namiki, Hideo Kondo, Tadashi Semba, Kentaro Aburatani, Hiroyuki Taya, Yoichi Nakagama, Hitoshi Ohki, Rieko |
author_facet | Ezawa, Issei Sawai, Yuichiro Kawase, Tatsuya Okabe, Atsushi Tsutsumi, Shuichi Ichikawa, Hitoshi Kobayashi, Yuka Tashiro, Fumio Namiki, Hideo Kondo, Tadashi Semba, Kentaro Aburatani, Hiroyuki Taya, Yoichi Nakagama, Hitoshi Ohki, Rieko |
author_sort | Ezawa, Issei |
collection | PubMed |
description | The tumor suppressor p53 functions by inducing the transcription of a collection of target genes. We previously attempted to identify p53 target genes by microarray expression and ChIP‐sequencing analyses. In this study, we describe a novel p53 target gene, FUCA1, which encodes a fucosidase. Although fucosidase, α‐l‐1 (FUCA1) has been reported to be a lysosomal protein, we detected it outside of lysosomes and observed that its activity is highest at physiological pH. As there is a reported association between fucosylation and tumorigenesis, we investigated the potential role of FUCA1 in cancer. We found that overexpression of FUCA1, but not a mutant defective in enzyme activity, suppressed the growth of cancer cells and induced cell death. Furthermore, we showed that FUCA1 reduced fucosylation and activation of epidermal growth factor receptor, and concomitantly suppressed epidermal growth factor signaling pathways. FUCA1 loss‐of‐function mutations are found in several cancers, its expression is reduced in cancers of the large intestine, and low FUCA1 expression is associated with poorer prognosis in several cancers. These results show that protein defucosylation mediated by FUCA1 is involved in tumor suppression. |
format | Online Article Text |
id | pubmed-4968591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49685912016-08-10 Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells Ezawa, Issei Sawai, Yuichiro Kawase, Tatsuya Okabe, Atsushi Tsutsumi, Shuichi Ichikawa, Hitoshi Kobayashi, Yuka Tashiro, Fumio Namiki, Hideo Kondo, Tadashi Semba, Kentaro Aburatani, Hiroyuki Taya, Yoichi Nakagama, Hitoshi Ohki, Rieko Cancer Sci Original Articles The tumor suppressor p53 functions by inducing the transcription of a collection of target genes. We previously attempted to identify p53 target genes by microarray expression and ChIP‐sequencing analyses. In this study, we describe a novel p53 target gene, FUCA1, which encodes a fucosidase. Although fucosidase, α‐l‐1 (FUCA1) has been reported to be a lysosomal protein, we detected it outside of lysosomes and observed that its activity is highest at physiological pH. As there is a reported association between fucosylation and tumorigenesis, we investigated the potential role of FUCA1 in cancer. We found that overexpression of FUCA1, but not a mutant defective in enzyme activity, suppressed the growth of cancer cells and induced cell death. Furthermore, we showed that FUCA1 reduced fucosylation and activation of epidermal growth factor receptor, and concomitantly suppressed epidermal growth factor signaling pathways. FUCA1 loss‐of‐function mutations are found in several cancers, its expression is reduced in cancers of the large intestine, and low FUCA1 expression is associated with poorer prognosis in several cancers. These results show that protein defucosylation mediated by FUCA1 is involved in tumor suppression. John Wiley and Sons Inc. 2016-05-16 2016-06 /pmc/articles/PMC4968591/ /pubmed/26998741 http://dx.doi.org/10.1111/cas.12933 Text en © 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Ezawa, Issei Sawai, Yuichiro Kawase, Tatsuya Okabe, Atsushi Tsutsumi, Shuichi Ichikawa, Hitoshi Kobayashi, Yuka Tashiro, Fumio Namiki, Hideo Kondo, Tadashi Semba, Kentaro Aburatani, Hiroyuki Taya, Yoichi Nakagama, Hitoshi Ohki, Rieko Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells |
title | Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells |
title_full | Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells |
title_fullStr | Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells |
title_full_unstemmed | Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells |
title_short | Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells |
title_sort | novel p53 target gene fuca1 encodes a fucosidase and regulates growth and survival of cancer cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968591/ https://www.ncbi.nlm.nih.gov/pubmed/26998741 http://dx.doi.org/10.1111/cas.12933 |
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