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Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis
Chondrosarcoma is a malignancy of soft tissue and bone that has a high propensity to metastasize to distant organs. Nerve growth factor (NGF) is critical for neuronal cell growth, apoptosis, and differentiation, and also appears to promote the progression and metastasis of several different types of...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611026/ https://www.ncbi.nlm.nih.gov/pubmed/34815382 http://dx.doi.org/10.1038/s41419-021-04392-2 |
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author | Tzeng, Huey-En Lin, Syuan-Ling Thadevoos, Louis Anoop Lien, Ming-Yu Yang, Wei-Hung Ko, Chih-Yuan Lin, Chih-Yang Huang, Yu-Wen Liu, Ju-Fang Fong, Yi-Chin Chen, Hsien-Te Tang, Chih-Hsin |
author_facet | Tzeng, Huey-En Lin, Syuan-Ling Thadevoos, Louis Anoop Lien, Ming-Yu Yang, Wei-Hung Ko, Chih-Yuan Lin, Chih-Yang Huang, Yu-Wen Liu, Ju-Fang Fong, Yi-Chin Chen, Hsien-Te Tang, Chih-Hsin |
author_sort | Tzeng, Huey-En |
collection | PubMed |
description | Chondrosarcoma is a malignancy of soft tissue and bone that has a high propensity to metastasize to distant organs. Nerve growth factor (NGF) is critical for neuronal cell growth, apoptosis, and differentiation, and also appears to promote the progression and metastasis of several different types of tumors, although the effects of NGF upon chondrosarcoma mechanisms are not very clear. We report that NGF facilitates lysyl oxidase (LOX)-dependent cellular migration and invasion in human chondrosarcoma cells, and that NGF overexpression enhances lung metastasis in a mouse model of chondrosarcoma. NGF-induced stimulation of LOX production and cell motility occurs through the inhibition of miR-149-5p expression, which was reversed by PI3K, Akt, and mTOR inhibitors and their respective short interfering RNAs. Notably, levels of NGF and LOX expression correlated with tumor stage in human chondrosarcoma samples. Thus, NGF appears to be a worthwhile therapeutic target for metastatic chondrosarcoma. |
format | Online Article Text |
id | pubmed-8611026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86110262021-12-01 Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis Tzeng, Huey-En Lin, Syuan-Ling Thadevoos, Louis Anoop Lien, Ming-Yu Yang, Wei-Hung Ko, Chih-Yuan Lin, Chih-Yang Huang, Yu-Wen Liu, Ju-Fang Fong, Yi-Chin Chen, Hsien-Te Tang, Chih-Hsin Cell Death Dis Article Chondrosarcoma is a malignancy of soft tissue and bone that has a high propensity to metastasize to distant organs. Nerve growth factor (NGF) is critical for neuronal cell growth, apoptosis, and differentiation, and also appears to promote the progression and metastasis of several different types of tumors, although the effects of NGF upon chondrosarcoma mechanisms are not very clear. We report that NGF facilitates lysyl oxidase (LOX)-dependent cellular migration and invasion in human chondrosarcoma cells, and that NGF overexpression enhances lung metastasis in a mouse model of chondrosarcoma. NGF-induced stimulation of LOX production and cell motility occurs through the inhibition of miR-149-5p expression, which was reversed by PI3K, Akt, and mTOR inhibitors and their respective short interfering RNAs. Notably, levels of NGF and LOX expression correlated with tumor stage in human chondrosarcoma samples. Thus, NGF appears to be a worthwhile therapeutic target for metastatic chondrosarcoma. Nature Publishing Group UK 2021-11-23 /pmc/articles/PMC8611026/ /pubmed/34815382 http://dx.doi.org/10.1038/s41419-021-04392-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tzeng, Huey-En Lin, Syuan-Ling Thadevoos, Louis Anoop Lien, Ming-Yu Yang, Wei-Hung Ko, Chih-Yuan Lin, Chih-Yang Huang, Yu-Wen Liu, Ju-Fang Fong, Yi-Chin Chen, Hsien-Te Tang, Chih-Hsin Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis |
title | Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis |
title_full | Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis |
title_fullStr | Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis |
title_full_unstemmed | Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis |
title_short | Nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing miR-149-5p synthesis |
title_sort | nerve growth factor promotes lysyl oxidase-dependent chondrosarcoma cell metastasis by suppressing mir-149-5p synthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611026/ https://www.ncbi.nlm.nih.gov/pubmed/34815382 http://dx.doi.org/10.1038/s41419-021-04392-2 |
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