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Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis
AIM: The purpose of this study is to consider the function of cytoskeleton-associated protein 2-like (CKAP2L) in lung adenocarcinoma (LAD) development and its prognostic value. METHODS: The mRNA expression of CKAP2L and its correlation with clinical factors in LAD patients were analyzed from the dat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388994/ https://www.ncbi.nlm.nih.gov/pubmed/30863084 http://dx.doi.org/10.2147/OTT.S182242 |
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author | Xiong, Guosheng Li, Liyin Chen, Xiaobo Song, Sinuo Zhao, Yunping Cai, Wenke Peng, Jingping |
author_facet | Xiong, Guosheng Li, Liyin Chen, Xiaobo Song, Sinuo Zhao, Yunping Cai, Wenke Peng, Jingping |
author_sort | Xiong, Guosheng |
collection | PubMed |
description | AIM: The purpose of this study is to consider the function of cytoskeleton-associated protein 2-like (CKAP2L) in lung adenocarcinoma (LAD) development and its prognostic value. METHODS: The mRNA expression of CKAP2L and its correlation with clinical factors in LAD patients were analyzed from the data taken from The Cancer Genome Atlas and The First Affiliated Hospital of Kunming Medical University. We constructed H460 and A549 cell lines with silenced CKAP2L using RNA interference. Cell counting kit-8 assay and colony formation assays were carried out to determine the function of CKAP2L in H460 and A549 cell proliferation. Transwell and wound healing assays were applied to determine the effect of CKAP2L on H460 and A549 cell invasion and migration. The influences of CKAP2L on mitogen-activated protein kinase signaling pathway-related proteins were tested by Western blotting. RESULTS: CKAP2L expression is enhanced in LAD tissues and is predictive of poor prognosis in LAD patients. High expression of CKAP2L is associated with stage (P<0.001), lymph node status (P=0.002), and metastasis (P=0.025). Depletion of CKAP2L dramatically suppressed the proliferation, migration, and invasion of H460 and A549 cells. Moreover, the ratio of p-MEK/ MEK and p-ERK/ERK reduced obviously in A549 cells after depleting CKAP2L. CONCLUSION: Our findings implied that CKAP2L might be a promoter of LAD and could serve as a predictor for LAD patients. |
format | Online Article Text |
id | pubmed-6388994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63889942019-03-12 Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis Xiong, Guosheng Li, Liyin Chen, Xiaobo Song, Sinuo Zhao, Yunping Cai, Wenke Peng, Jingping Onco Targets Ther Original Research AIM: The purpose of this study is to consider the function of cytoskeleton-associated protein 2-like (CKAP2L) in lung adenocarcinoma (LAD) development and its prognostic value. METHODS: The mRNA expression of CKAP2L and its correlation with clinical factors in LAD patients were analyzed from the data taken from The Cancer Genome Atlas and The First Affiliated Hospital of Kunming Medical University. We constructed H460 and A549 cell lines with silenced CKAP2L using RNA interference. Cell counting kit-8 assay and colony formation assays were carried out to determine the function of CKAP2L in H460 and A549 cell proliferation. Transwell and wound healing assays were applied to determine the effect of CKAP2L on H460 and A549 cell invasion and migration. The influences of CKAP2L on mitogen-activated protein kinase signaling pathway-related proteins were tested by Western blotting. RESULTS: CKAP2L expression is enhanced in LAD tissues and is predictive of poor prognosis in LAD patients. High expression of CKAP2L is associated with stage (P<0.001), lymph node status (P=0.002), and metastasis (P=0.025). Depletion of CKAP2L dramatically suppressed the proliferation, migration, and invasion of H460 and A549 cells. Moreover, the ratio of p-MEK/ MEK and p-ERK/ERK reduced obviously in A549 cells after depleting CKAP2L. CONCLUSION: Our findings implied that CKAP2L might be a promoter of LAD and could serve as a predictor for LAD patients. Dove Medical Press 2019-02-12 /pmc/articles/PMC6388994/ /pubmed/30863084 http://dx.doi.org/10.2147/OTT.S182242 Text en © 2019 Xiong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Xiong, Guosheng Li, Liyin Chen, Xiaobo Song, Sinuo Zhao, Yunping Cai, Wenke Peng, Jingping Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
title | Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
title_full | Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
title_fullStr | Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
title_full_unstemmed | Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
title_short | Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
title_sort | up-regulation of ckap2l expression promotes lung adenocarcinoma invasion and is associated with poor prognosis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388994/ https://www.ncbi.nlm.nih.gov/pubmed/30863084 http://dx.doi.org/10.2147/OTT.S182242 |
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