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UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling
BACKGROUND: UFM1 has been found to be involved in the regulation of tumor development. This study aims to clarify the role and potential molecular mechanisms of UFM1 in the invasion and metastasis of gastric cancer. METHODS: Expression of UFM1 in gastric tumor and paired adjacent noncancerous tissue...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751655/ https://www.ncbi.nlm.nih.gov/pubmed/31533855 http://dx.doi.org/10.1186/s13046-019-1416-4 |
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author | Lin, Jian-Xian Xie, Xin-Sheng Weng, Xiong-Feng Qiu, Sheng-Liang Yoon, Changhwan Lian, Ning-Zi Xie, Jian-Wei Wang, Jia-Bin Lu, Jun Chen, Qi-Yue Cao, Long-Long Lin, Mi Tu, Ru-Hong Yang, Ying-Hong Huang, Chang-Ming Zheng, Chao-Hui Li, Ping |
author_facet | Lin, Jian-Xian Xie, Xin-Sheng Weng, Xiong-Feng Qiu, Sheng-Liang Yoon, Changhwan Lian, Ning-Zi Xie, Jian-Wei Wang, Jia-Bin Lu, Jun Chen, Qi-Yue Cao, Long-Long Lin, Mi Tu, Ru-Hong Yang, Ying-Hong Huang, Chang-Ming Zheng, Chao-Hui Li, Ping |
author_sort | Lin, Jian-Xian |
collection | PubMed |
description | BACKGROUND: UFM1 has been found to be involved in the regulation of tumor development. This study aims to clarify the role and potential molecular mechanisms of UFM1 in the invasion and metastasis of gastric cancer. METHODS: Expression of UFM1 in gastric tumor and paired adjacent noncancerous tissues from 437 patients was analyzed by Western blotting, immunohistochemistry, and realtime PCR. Its correlation with the clinicopathological characteristics and prognosis of gastric cancer patients was analyzed. The effects of UFM1 on the invasion and migration of gastric cancer cells were determined by the wound and trans-well assays, and the effect of UFM1 on subcutaneous tumor formation was verified in nude mice. The potential downstream targets of UFM1 and related molecular mechanisms were clarified by the human protein kinase assay and co-immunoprecipitation technique. RESULTS: Compared with the corresponding adjacent tissues, the transcription level and protein expression level of UFM1 in gastric cancer tissues were significantly downregulated (P < 0.05). The 5-year survival rate of gastric cancer patients with low UFM1 expression was significantly lower than the patients with high UFM1 expression (42.1% vs 63.0%, P < 0.05). The invasion and migration abilities of gastric cancer cells with stable UFM1 overexpression were significantly decreased, and the gastric cancer cells with UFM1 stable knockdown showed the opposite results; similar results were also obtained in the nude mouse model. Further studies have revealed that UFM1 could increase the ubiquitination level of PDK1 and decrease the expression of PDK1 at protein level, thereby inhibiting the phosphorylation level of AKT at Ser473. Additionally, the effect of UFM1 on gastric cancer cell function is dependent on the expression of PDK1. The expression level of UFM1 can improve the poor prognosis of PDK1 in patients with gastric cancer. CONCLUSION: UFM1 suppresses the invasion and metastasis of gastric cancer by increasing the ubiquitination of PDK1 through negatively regulating PI3K/AKT signaling. |
format | Online Article Text |
id | pubmed-6751655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67516552019-09-23 UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling Lin, Jian-Xian Xie, Xin-Sheng Weng, Xiong-Feng Qiu, Sheng-Liang Yoon, Changhwan Lian, Ning-Zi Xie, Jian-Wei Wang, Jia-Bin Lu, Jun Chen, Qi-Yue Cao, Long-Long Lin, Mi Tu, Ru-Hong Yang, Ying-Hong Huang, Chang-Ming Zheng, Chao-Hui Li, Ping J Exp Clin Cancer Res Research BACKGROUND: UFM1 has been found to be involved in the regulation of tumor development. This study aims to clarify the role and potential molecular mechanisms of UFM1 in the invasion and metastasis of gastric cancer. METHODS: Expression of UFM1 in gastric tumor and paired adjacent noncancerous tissues from 437 patients was analyzed by Western blotting, immunohistochemistry, and realtime PCR. Its correlation with the clinicopathological characteristics and prognosis of gastric cancer patients was analyzed. The effects of UFM1 on the invasion and migration of gastric cancer cells were determined by the wound and trans-well assays, and the effect of UFM1 on subcutaneous tumor formation was verified in nude mice. The potential downstream targets of UFM1 and related molecular mechanisms were clarified by the human protein kinase assay and co-immunoprecipitation technique. RESULTS: Compared with the corresponding adjacent tissues, the transcription level and protein expression level of UFM1 in gastric cancer tissues were significantly downregulated (P < 0.05). The 5-year survival rate of gastric cancer patients with low UFM1 expression was significantly lower than the patients with high UFM1 expression (42.1% vs 63.0%, P < 0.05). The invasion and migration abilities of gastric cancer cells with stable UFM1 overexpression were significantly decreased, and the gastric cancer cells with UFM1 stable knockdown showed the opposite results; similar results were also obtained in the nude mouse model. Further studies have revealed that UFM1 could increase the ubiquitination level of PDK1 and decrease the expression of PDK1 at protein level, thereby inhibiting the phosphorylation level of AKT at Ser473. Additionally, the effect of UFM1 on gastric cancer cell function is dependent on the expression of PDK1. The expression level of UFM1 can improve the poor prognosis of PDK1 in patients with gastric cancer. CONCLUSION: UFM1 suppresses the invasion and metastasis of gastric cancer by increasing the ubiquitination of PDK1 through negatively regulating PI3K/AKT signaling. BioMed Central 2019-09-18 /pmc/articles/PMC6751655/ /pubmed/31533855 http://dx.doi.org/10.1186/s13046-019-1416-4 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lin, Jian-Xian Xie, Xin-Sheng Weng, Xiong-Feng Qiu, Sheng-Liang Yoon, Changhwan Lian, Ning-Zi Xie, Jian-Wei Wang, Jia-Bin Lu, Jun Chen, Qi-Yue Cao, Long-Long Lin, Mi Tu, Ru-Hong Yang, Ying-Hong Huang, Chang-Ming Zheng, Chao-Hui Li, Ping UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling |
title | UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling |
title_full | UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling |
title_fullStr | UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling |
title_full_unstemmed | UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling |
title_short | UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling |
title_sort | ufm1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of pdk1 through pi3k/akt signaling |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751655/ https://www.ncbi.nlm.nih.gov/pubmed/31533855 http://dx.doi.org/10.1186/s13046-019-1416-4 |
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