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CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma
BACKGROUND: Adenocarcinoma is a non–small-cell lung cancer that is common cancer in both genders, and has poor clinical outcomes. We aimed to evaluate the role of cytoskeleton-associated protein 2 (CKAP2), its prognostic significance, and the relationship between CKAP2 expression and lung adenocarci...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333529/ https://www.ncbi.nlm.nih.gov/pubmed/35905213 http://dx.doi.org/10.1097/MD.0000000000029796 |
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author | Zhang, Sen Li, Na Yang, Yonghua Li, Yan Lin, Chenshi Fu, Guoquan Cai, Jun |
author_facet | Zhang, Sen Li, Na Yang, Yonghua Li, Yan Lin, Chenshi Fu, Guoquan Cai, Jun |
author_sort | Zhang, Sen |
collection | PubMed |
description | BACKGROUND: Adenocarcinoma is a non–small-cell lung cancer that is common cancer in both genders, and has poor clinical outcomes. We aimed to evaluate the role of cytoskeleton-associated protein 2 (CKAP2), its prognostic significance, and the relationship between CKAP2 expression and lung adenocarcinoma driver genes. METHODS: The expression of CKAP2 was studied by immunohistochemical staining of specimens from 88 patients with lung adenocarcinoma. The correlation between clinicopathological features and CKAP2 expression was analyzed. Kaplan-Meier analysis and Cox proportional hazard models were used to examine the prognostic value of CKAP2 in terms of overall survival (OS). The correlation between epidermal growth factor receptor (EGFR) mutation, anaplastic lymphoma kinase (ALK) rearrangement, and CKAP2 expression was analyzed. All histological samples were detected by fluorescence in situ hybridization for EGFR mutations and ALK rearrangements. RESULTS: Eighty-eight patients with positive CKAP2 expression were observed in this study. Patients with high levels of CKAP2 expression were associated with OS (P = .021). Multivariate Cox regression analysis disclosed that positive CKAP2 expression (P = .043) could independently predict unfavorable OS. In addition, CKAP2 expression was not associated with EGFR mutation (P = .219) and ALK rearrangement (P = .389) in lung adenocarcinoma patients. CONCLUSION: High expression of CKAP2 may serve as a marker of poor prognosis in lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-9333529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-93335292022-08-03 CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma Zhang, Sen Li, Na Yang, Yonghua Li, Yan Lin, Chenshi Fu, Guoquan Cai, Jun Medicine (Baltimore) Research Article BACKGROUND: Adenocarcinoma is a non–small-cell lung cancer that is common cancer in both genders, and has poor clinical outcomes. We aimed to evaluate the role of cytoskeleton-associated protein 2 (CKAP2), its prognostic significance, and the relationship between CKAP2 expression and lung adenocarcinoma driver genes. METHODS: The expression of CKAP2 was studied by immunohistochemical staining of specimens from 88 patients with lung adenocarcinoma. The correlation between clinicopathological features and CKAP2 expression was analyzed. Kaplan-Meier analysis and Cox proportional hazard models were used to examine the prognostic value of CKAP2 in terms of overall survival (OS). The correlation between epidermal growth factor receptor (EGFR) mutation, anaplastic lymphoma kinase (ALK) rearrangement, and CKAP2 expression was analyzed. All histological samples were detected by fluorescence in situ hybridization for EGFR mutations and ALK rearrangements. RESULTS: Eighty-eight patients with positive CKAP2 expression were observed in this study. Patients with high levels of CKAP2 expression were associated with OS (P = .021). Multivariate Cox regression analysis disclosed that positive CKAP2 expression (P = .043) could independently predict unfavorable OS. In addition, CKAP2 expression was not associated with EGFR mutation (P = .219) and ALK rearrangement (P = .389) in lung adenocarcinoma patients. CONCLUSION: High expression of CKAP2 may serve as a marker of poor prognosis in lung adenocarcinoma. Lippincott Williams & Wilkins 2022-07-29 /pmc/articles/PMC9333529/ /pubmed/35905213 http://dx.doi.org/10.1097/MD.0000000000029796 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | Research Article Zhang, Sen Li, Na Yang, Yonghua Li, Yan Lin, Chenshi Fu, Guoquan Cai, Jun CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
title | CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
title_full | CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
title_fullStr | CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
title_full_unstemmed | CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
title_short | CKAP2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
title_sort | ckap2 overexpression correlates with worse overall survival in patients with lung adenocarcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333529/ https://www.ncbi.nlm.nih.gov/pubmed/35905213 http://dx.doi.org/10.1097/MD.0000000000029796 |
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