Cargando…
Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study
Cervical cancer is one of the most common malignant tumor in women. The mechanisms of cervical cancer are intricate and have not been fully understood. Therefore, we employed iTRAQ to obtain novel proteins profile which participates in the tumor oncogenesis of cervical cancer. 3300 proteins were ide...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342753/ https://www.ncbi.nlm.nih.gov/pubmed/27690342 http://dx.doi.org/10.18632/oncotarget.12258 |
_version_ | 1782513247105056768 |
---|---|
author | Liu, Shuaibin Hao, Xiaoming Ouyang, Xiaolan Dong, Xiaojing Yang, Yixuan Yu, Tinghe Hu, Jianguo Hu, Lina |
author_facet | Liu, Shuaibin Hao, Xiaoming Ouyang, Xiaolan Dong, Xiaojing Yang, Yixuan Yu, Tinghe Hu, Jianguo Hu, Lina |
author_sort | Liu, Shuaibin |
collection | PubMed |
description | Cervical cancer is one of the most common malignant tumor in women. The mechanisms of cervical cancer are intricate and have not been fully understood. Therefore, we employed iTRAQ to obtain novel proteins profile which participates in the tumor oncogenesis of cervical cancer. 3300 proteins were identified aberrantly expressed in cervical cancer, and western bolt was performed to validate the results of iTRAQ. Then, we selected LYN for further study. Immunohistochemistry identified that LYN expression was significantly increased in cervical cancer tissues than that in cancer adjacent normal cervical tissues and normal cervical tissues. The increased LYN expression was significantly correlated with cancer differentiation and FIGO stage. Silencing LYN inhibited cell proliferation, migration and invasion, conversely, overexpression LYN promoted cell proliferation, migration and invasion. In terms of mechanism, LYN could also promote cervical cancer cells metastasis through activating IL-6/STAT3 pathway. In vivo study, overexpression LYN promoted tumor growth, meanwhile knockdown LYN inhibited tumor growth. These results indicate that LYN tyrosine kinase is an oncogenic gene and can serve as a novel target for cervical cancer research and therapy. |
format | Online Article Text |
id | pubmed-5342753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53427532017-03-28 Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study Liu, Shuaibin Hao, Xiaoming Ouyang, Xiaolan Dong, Xiaojing Yang, Yixuan Yu, Tinghe Hu, Jianguo Hu, Lina Oncotarget Research Paper Cervical cancer is one of the most common malignant tumor in women. The mechanisms of cervical cancer are intricate and have not been fully understood. Therefore, we employed iTRAQ to obtain novel proteins profile which participates in the tumor oncogenesis of cervical cancer. 3300 proteins were identified aberrantly expressed in cervical cancer, and western bolt was performed to validate the results of iTRAQ. Then, we selected LYN for further study. Immunohistochemistry identified that LYN expression was significantly increased in cervical cancer tissues than that in cancer adjacent normal cervical tissues and normal cervical tissues. The increased LYN expression was significantly correlated with cancer differentiation and FIGO stage. Silencing LYN inhibited cell proliferation, migration and invasion, conversely, overexpression LYN promoted cell proliferation, migration and invasion. In terms of mechanism, LYN could also promote cervical cancer cells metastasis through activating IL-6/STAT3 pathway. In vivo study, overexpression LYN promoted tumor growth, meanwhile knockdown LYN inhibited tumor growth. These results indicate that LYN tyrosine kinase is an oncogenic gene and can serve as a novel target for cervical cancer research and therapy. Impact Journals LLC 2016-09-26 /pmc/articles/PMC5342753/ /pubmed/27690342 http://dx.doi.org/10.18632/oncotarget.12258 Text en Copyright: © 2016 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Shuaibin Hao, Xiaoming Ouyang, Xiaolan Dong, Xiaojing Yang, Yixuan Yu, Tinghe Hu, Jianguo Hu, Lina Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study |
title | Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study |
title_full | Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study |
title_fullStr | Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study |
title_full_unstemmed | Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study |
title_short | Tyrosine kinase LYN is an oncotarget in human cervical cancer: A quantitative proteomic based study |
title_sort | tyrosine kinase lyn is an oncotarget in human cervical cancer: a quantitative proteomic based study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342753/ https://www.ncbi.nlm.nih.gov/pubmed/27690342 http://dx.doi.org/10.18632/oncotarget.12258 |
work_keys_str_mv | AT liushuaibin tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT haoxiaoming tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT ouyangxiaolan tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT dongxiaojing tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT yangyixuan tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT yutinghe tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT hujianguo tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy AT hulina tyrosinekinaselynisanoncotargetinhumancervicalcanceraquantitativeproteomicbasedstudy |