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Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer
Bioactive sphingolipid is clearly relevant to lung physiology. The relationship of the bioactive sphingolipid pathway to pulmonary disease has been studied in cellular, tissue, and animal model, including lung cancer models. The samples of 53 patients diagnosed with nonsmall cell lung carcinoma (NSC...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879003/ https://www.ncbi.nlm.nih.gov/pubmed/33623898 http://dx.doi.org/10.1177/2632010X20988531 |
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author | Motono, Nozomu Ueda, Yoshimichi Shimasaki, Miyako Iwai, Shun Iijima, Yoshihito Usuda, Katsuo Uramoto, Hidetaka |
author_facet | Motono, Nozomu Ueda, Yoshimichi Shimasaki, Miyako Iwai, Shun Iijima, Yoshihito Usuda, Katsuo Uramoto, Hidetaka |
author_sort | Motono, Nozomu |
collection | PubMed |
description | Bioactive sphingolipid is clearly relevant to lung physiology. The relationship of the bioactive sphingolipid pathway to pulmonary disease has been studied in cellular, tissue, and animal model, including lung cancer models. The samples of 53 patients diagnosed with nonsmall cell lung carcinoma (NSCLC) between June 2009 and May 2014 at our hospital were analyzed. Immunohistochemical (IHC) analysis was performed. The degree of immunostaining was reviewed and scored. Using this method of assessment, we evaluated the IHC score of sphingosine kinase 1 (SPHK1), vimentin, E-cadherin, and Ki-67. Both invasive adenocarcinoma cell and squamous cell carcinoma cell were well stained by SPHK1, and fibroblasts were also well stained by SPHK1. Although the IHC score of SPHK1 was not significantly differed between invasive adenocarcinoma and squamous cell carcinoma, the IHC scores of fibroblast, vimentin, and Ki-67 were higher in squamous cell carcinoma than invasive adenocarcinoma. Correlation among IHC scores in each of invasive adenocarcinoma and squamous cell carcinoma was performed. SPHK1 had positive correlation with both fibroblast and Ki-67, and fibroblast and Ki-67 had also positive correlation in invasive adenocarcinoma. On the contrary, SPHK1 had no significant correlation with fibroblast, and had negative correlation with Ki-67 in squamous cell carcinoma. Although there was not significant prognostic difference in SPHK1 score (P = .09), IHC score high group tended to be worse on relapse-free survival. SPHK1 might be prognostic factor in lung-invasive adenocarcinoma and novel target for drug against lung-invasive adenocarcinoma. |
format | Online Article Text |
id | pubmed-7879003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78790032021-02-22 Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer Motono, Nozomu Ueda, Yoshimichi Shimasaki, Miyako Iwai, Shun Iijima, Yoshihito Usuda, Katsuo Uramoto, Hidetaka Clin Pathol Focus Section: Novel Therapies Bioactive sphingolipid is clearly relevant to lung physiology. The relationship of the bioactive sphingolipid pathway to pulmonary disease has been studied in cellular, tissue, and animal model, including lung cancer models. The samples of 53 patients diagnosed with nonsmall cell lung carcinoma (NSCLC) between June 2009 and May 2014 at our hospital were analyzed. Immunohistochemical (IHC) analysis was performed. The degree of immunostaining was reviewed and scored. Using this method of assessment, we evaluated the IHC score of sphingosine kinase 1 (SPHK1), vimentin, E-cadherin, and Ki-67. Both invasive adenocarcinoma cell and squamous cell carcinoma cell were well stained by SPHK1, and fibroblasts were also well stained by SPHK1. Although the IHC score of SPHK1 was not significantly differed between invasive adenocarcinoma and squamous cell carcinoma, the IHC scores of fibroblast, vimentin, and Ki-67 were higher in squamous cell carcinoma than invasive adenocarcinoma. Correlation among IHC scores in each of invasive adenocarcinoma and squamous cell carcinoma was performed. SPHK1 had positive correlation with both fibroblast and Ki-67, and fibroblast and Ki-67 had also positive correlation in invasive adenocarcinoma. On the contrary, SPHK1 had no significant correlation with fibroblast, and had negative correlation with Ki-67 in squamous cell carcinoma. Although there was not significant prognostic difference in SPHK1 score (P = .09), IHC score high group tended to be worse on relapse-free survival. SPHK1 might be prognostic factor in lung-invasive adenocarcinoma and novel target for drug against lung-invasive adenocarcinoma. SAGE Publications 2021-02-10 /pmc/articles/PMC7879003/ /pubmed/33623898 http://dx.doi.org/10.1177/2632010X20988531 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Focus Section: Novel Therapies Motono, Nozomu Ueda, Yoshimichi Shimasaki, Miyako Iwai, Shun Iijima, Yoshihito Usuda, Katsuo Uramoto, Hidetaka Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer |
title | Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer |
title_full | Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer |
title_fullStr | Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer |
title_full_unstemmed | Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer |
title_short | Prognostic Impact of Sphingosine Kinase 1 in Nonsmall Cell Lung Cancer |
title_sort | prognostic impact of sphingosine kinase 1 in nonsmall cell lung cancer |
topic | Focus Section: Novel Therapies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879003/ https://www.ncbi.nlm.nih.gov/pubmed/33623898 http://dx.doi.org/10.1177/2632010X20988531 |
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