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Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis

BACKGROUND: To investigate the expression of neuro-oncological ventral antigen-1 (Nova1) in small-cell lung cancer (SCLC) and its value in clinical pathological diagnosis of SCLCs. METHODS: Nova1 expression in the SCLC cell line H446, lung adenocarcinoma cell line A549, squamous cell carcinoma (SCC)...

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Autores principales: Deng, Shuangshuang, Liu, Meixuan, Xiao, Tianyu, Gao, Jinli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799250/
https://www.ncbi.nlm.nih.gov/pubmed/35117458
http://dx.doi.org/10.21037/tcr.2019.12.99
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author Deng, Shuangshuang
Liu, Meixuan
Xiao, Tianyu
Gao, Jinli
author_facet Deng, Shuangshuang
Liu, Meixuan
Xiao, Tianyu
Gao, Jinli
author_sort Deng, Shuangshuang
collection PubMed
description BACKGROUND: To investigate the expression of neuro-oncological ventral antigen-1 (Nova1) in small-cell lung cancer (SCLC) and its value in clinical pathological diagnosis of SCLCs. METHODS: Nova1 expression in the SCLC cell line H446, lung adenocarcinoma cell line A549, squamous cell carcinoma (SCC) cell line H226 and bronchial epithelial cell line BEAS-2B were examined by RT-PCR. It’s expression in paraffin specimens of 100 SCLC cases, 15 specimens of lung adenocarcinoma cases and 15 specimens of lung SCC cases, as well as adjacent normal tissue was determined by immunohistochemistry. The positive rate of Nova1 in SCLC tissue was compared with those of traditional neuroendocrine markers CD56, Syn and CgA. RESULTS: Nova1 expression in SCLC cell line H446 was significantly higher than that of bronchial epithelial cell line BEAS-2B and lung adenocarcinoma cell line A549 and SCC cell line H226. The positive rate of Nova1 in SCLC tissue was similar to that of CD56 but higher than those of Syn and CgA. Nova1 was neither expressed in the cancer tissue nor in the adjacent normal tissue of the 15 cases of SCC and the 15 cases of adenocarcinoma. In all six cases of combined SCLC, Nova1 was expressed in the SCLC component, whereas markers of SCC or adenocarcinoma were absent. CONCLUSIONS: Nova1 can be used as a novel neuroendocrine marker for pathological diagnosis of SCLC in clinical practice with high sensitivity and specificity, in addition to its role as an independent prognostic marker of overall survival and tumour recurrence, as suggested by previous studies.
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spelling pubmed-87992502022-02-02 Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis Deng, Shuangshuang Liu, Meixuan Xiao, Tianyu Gao, Jinli Transl Cancer Res Original Article BACKGROUND: To investigate the expression of neuro-oncological ventral antigen-1 (Nova1) in small-cell lung cancer (SCLC) and its value in clinical pathological diagnosis of SCLCs. METHODS: Nova1 expression in the SCLC cell line H446, lung adenocarcinoma cell line A549, squamous cell carcinoma (SCC) cell line H226 and bronchial epithelial cell line BEAS-2B were examined by RT-PCR. It’s expression in paraffin specimens of 100 SCLC cases, 15 specimens of lung adenocarcinoma cases and 15 specimens of lung SCC cases, as well as adjacent normal tissue was determined by immunohistochemistry. The positive rate of Nova1 in SCLC tissue was compared with those of traditional neuroendocrine markers CD56, Syn and CgA. RESULTS: Nova1 expression in SCLC cell line H446 was significantly higher than that of bronchial epithelial cell line BEAS-2B and lung adenocarcinoma cell line A549 and SCC cell line H226. The positive rate of Nova1 in SCLC tissue was similar to that of CD56 but higher than those of Syn and CgA. Nova1 was neither expressed in the cancer tissue nor in the adjacent normal tissue of the 15 cases of SCC and the 15 cases of adenocarcinoma. In all six cases of combined SCLC, Nova1 was expressed in the SCLC component, whereas markers of SCC or adenocarcinoma were absent. CONCLUSIONS: Nova1 can be used as a novel neuroendocrine marker for pathological diagnosis of SCLC in clinical practice with high sensitivity and specificity, in addition to its role as an independent prognostic marker of overall survival and tumour recurrence, as suggested by previous studies. AME Publishing Company 2020-02 /pmc/articles/PMC8799250/ /pubmed/35117458 http://dx.doi.org/10.21037/tcr.2019.12.99 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Deng, Shuangshuang
Liu, Meixuan
Xiao, Tianyu
Gao, Jinli
Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
title Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
title_full Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
title_fullStr Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
title_full_unstemmed Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
title_short Expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
title_sort expression of neuro-oncological ventral antigen-1 in small-cell lung cancer and its value in pathological diagnosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799250/
https://www.ncbi.nlm.nih.gov/pubmed/35117458
http://dx.doi.org/10.21037/tcr.2019.12.99
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