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High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma
Background: Primary adenosquamous carcinoma (ASC) is a rare malignant tumor in the lung and its biological behavior has not yet been thoroughly described. In this study, we aimed to explore the clinical and biological role of CXCR4 in patients with resected lung ASC. Methods: We retrospectively revi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959020/ https://www.ncbi.nlm.nih.gov/pubmed/31949484 http://dx.doi.org/10.7150/jca.36498 |
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author | Zhu, Qiaoliang Luo, Rongkui Gu, Jie Hou, Yingyong Chen, Zongwei Xu, Fengkai Wang, Lin Mao, Wei Lu, Chunlai Ge, Di |
author_facet | Zhu, Qiaoliang Luo, Rongkui Gu, Jie Hou, Yingyong Chen, Zongwei Xu, Fengkai Wang, Lin Mao, Wei Lu, Chunlai Ge, Di |
author_sort | Zhu, Qiaoliang |
collection | PubMed |
description | Background: Primary adenosquamous carcinoma (ASC) is a rare malignant tumor in the lung and its biological behavior has not yet been thoroughly described. In this study, we aimed to explore the clinical and biological role of CXCR4 in patients with resected lung ASC. Methods: We retrospectively reviewed the clinical records of patients with histologically confirmed lung ASC who underwent surgical resection with systematic lymph node dissection. Immunohistochemical staining was performed to detect the expression of CXCR4 in tumor tissues. The correlation between CXCR4 expression and clinicopathological characteristics were evaluated. The association between CXCR4 expression and patients' prognosis was analyzed by Kaplan-Meier and Cox regression. Moreover, we performed in vitro studies including CCK8, transwell and cell apoptosis to explore the potential role of CXCR4 in lung ASC. Results: A total of 78 patients with resected lung ASC were reviewed. Seventy (89.7%) patient tumors expressed CXCR4, with high level of CXCR4 expression observed in 45 (57.7%) cases. In vitro, CXCR4 conferred no difference in proliferative capacity but increased invasive potential, enhanced chemoresistance and inhibited apoptosis of lung ASC. Clinically, high CXCR4 expression was significantly associated with solid ASC, lymph node metastasis and advanced TNM stage. Patients with high CXCR4 expression and solid ASC had decreased disease-free survival and overall survival.Conclusions: CXCR4 was commonly expressed in lung ASC tumors. High CXCR4 expression might be a novel marker in predicting a poor prognosis in resected lung ASC and might serve as a potential therapeutic target. |
format | Online Article Text |
id | pubmed-6959020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-69590202020-01-16 High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma Zhu, Qiaoliang Luo, Rongkui Gu, Jie Hou, Yingyong Chen, Zongwei Xu, Fengkai Wang, Lin Mao, Wei Lu, Chunlai Ge, Di J Cancer Research Paper Background: Primary adenosquamous carcinoma (ASC) is a rare malignant tumor in the lung and its biological behavior has not yet been thoroughly described. In this study, we aimed to explore the clinical and biological role of CXCR4 in patients with resected lung ASC. Methods: We retrospectively reviewed the clinical records of patients with histologically confirmed lung ASC who underwent surgical resection with systematic lymph node dissection. Immunohistochemical staining was performed to detect the expression of CXCR4 in tumor tissues. The correlation between CXCR4 expression and clinicopathological characteristics were evaluated. The association between CXCR4 expression and patients' prognosis was analyzed by Kaplan-Meier and Cox regression. Moreover, we performed in vitro studies including CCK8, transwell and cell apoptosis to explore the potential role of CXCR4 in lung ASC. Results: A total of 78 patients with resected lung ASC were reviewed. Seventy (89.7%) patient tumors expressed CXCR4, with high level of CXCR4 expression observed in 45 (57.7%) cases. In vitro, CXCR4 conferred no difference in proliferative capacity but increased invasive potential, enhanced chemoresistance and inhibited apoptosis of lung ASC. Clinically, high CXCR4 expression was significantly associated with solid ASC, lymph node metastasis and advanced TNM stage. Patients with high CXCR4 expression and solid ASC had decreased disease-free survival and overall survival.Conclusions: CXCR4 was commonly expressed in lung ASC tumors. High CXCR4 expression might be a novel marker in predicting a poor prognosis in resected lung ASC and might serve as a potential therapeutic target. Ivyspring International Publisher 2020-01-01 /pmc/articles/PMC6959020/ /pubmed/31949484 http://dx.doi.org/10.7150/jca.36498 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Zhu, Qiaoliang Luo, Rongkui Gu, Jie Hou, Yingyong Chen, Zongwei Xu, Fengkai Wang, Lin Mao, Wei Lu, Chunlai Ge, Di High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma |
title | High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma |
title_full | High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma |
title_fullStr | High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma |
title_full_unstemmed | High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma |
title_short | High CXCR4 Expression Predicts a Poor Prognosis in Resected Lung Adenosquamous Carcinoma |
title_sort | high cxcr4 expression predicts a poor prognosis in resected lung adenosquamous carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959020/ https://www.ncbi.nlm.nih.gov/pubmed/31949484 http://dx.doi.org/10.7150/jca.36498 |
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