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Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma
BACKGROUND: Partner of Sld five 3 (Psf3) is a member of the heterotetrameric complex that consists of SLD5, Psf1, Psf2, and Psf3. We have shown in previous studies that high Psf3 expression was a poor prognostic marker for pulmonary adenocarcinoma. Here, we statistically evaluated the relationship b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885426/ https://www.ncbi.nlm.nih.gov/pubmed/31637868 http://dx.doi.org/10.1111/1759-7714.13230 |
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author | Kimura, Kenji Tanaka, Yugo Tauchi, Shunsuke Kitamura, Yoshitaka Nishio, Wataru Sakai, Yasuhiro Hayashi, Yoshitake Yoshimura, Masahiro Maniwa, Yoshimasa |
author_facet | Kimura, Kenji Tanaka, Yugo Tauchi, Shunsuke Kitamura, Yoshitaka Nishio, Wataru Sakai, Yasuhiro Hayashi, Yoshitake Yoshimura, Masahiro Maniwa, Yoshimasa |
author_sort | Kimura, Kenji |
collection | PubMed |
description | BACKGROUND: Partner of Sld five 3 (Psf3) is a member of the heterotetrameric complex that consists of SLD5, Psf1, Psf2, and Psf3. We have shown in previous studies that high Psf3 expression was a poor prognostic marker for pulmonary adenocarcinoma. Here, we statistically evaluated the relationship between clinicopathologic factors and Psf3 expression in stage I pulmonary adenocarcinoma. METHODS: A total of 583 patients who had undergone complete resection of stage I pulmonary adenocarcinoma from January 2002 to December 2009 were included in the study. Tissue microarrays were performed, and the resected tumors were divided into groups according to Psf3 expression. RESULTS: Of 583 patients, high expression of Psf3 was observed in 211 (36.2%) and low expression of Psf3 observed in 372 (63.8%) patients. Among stage I patients, the five‐year survival rate was 76.7% in the Psf3 high expression group and 90.9% in the Psf3 low expression group (P < 0.0001). On multivariate analysis, Psf3 was found to be the independent prognostic factor. Among stage I patients in the Psf3 high expression group, a significantly greater five‐year survival rate was observed in patients who received postoperative chemotherapy with tegafur‐uracil than in those who underwent surgery alone (P < 0.0001). In contrast, among stage I patients in the Psf3 low expression group, no difference was found in the five‐year survival, regardless of the presence or absence of tegafur‐uracil (P = 0.873). CONCLUSION: The Psf3 expression was an independent prognostic factor and could be a biomarker of adjuvant tegafur‐uracil for stage I pulmonary adenocarcinoma. KEY POINTS: Significant findings of the study: The Psf3 expression could be a biomarker of adjuvant tegafur‐uracil administration for stage I pulmonary adenocarcinoma. What this study adds: Appropriate patients of adjuvant chemotherapy for stage I pulmonary adenocarcinoma using Psf3 expression could be selected. |
format | Online Article Text |
id | pubmed-6885426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68854262019-12-09 Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma Kimura, Kenji Tanaka, Yugo Tauchi, Shunsuke Kitamura, Yoshitaka Nishio, Wataru Sakai, Yasuhiro Hayashi, Yoshitake Yoshimura, Masahiro Maniwa, Yoshimasa Thorac Cancer Original Articles BACKGROUND: Partner of Sld five 3 (Psf3) is a member of the heterotetrameric complex that consists of SLD5, Psf1, Psf2, and Psf3. We have shown in previous studies that high Psf3 expression was a poor prognostic marker for pulmonary adenocarcinoma. Here, we statistically evaluated the relationship between clinicopathologic factors and Psf3 expression in stage I pulmonary adenocarcinoma. METHODS: A total of 583 patients who had undergone complete resection of stage I pulmonary adenocarcinoma from January 2002 to December 2009 were included in the study. Tissue microarrays were performed, and the resected tumors were divided into groups according to Psf3 expression. RESULTS: Of 583 patients, high expression of Psf3 was observed in 211 (36.2%) and low expression of Psf3 observed in 372 (63.8%) patients. Among stage I patients, the five‐year survival rate was 76.7% in the Psf3 high expression group and 90.9% in the Psf3 low expression group (P < 0.0001). On multivariate analysis, Psf3 was found to be the independent prognostic factor. Among stage I patients in the Psf3 high expression group, a significantly greater five‐year survival rate was observed in patients who received postoperative chemotherapy with tegafur‐uracil than in those who underwent surgery alone (P < 0.0001). In contrast, among stage I patients in the Psf3 low expression group, no difference was found in the five‐year survival, regardless of the presence or absence of tegafur‐uracil (P = 0.873). CONCLUSION: The Psf3 expression was an independent prognostic factor and could be a biomarker of adjuvant tegafur‐uracil for stage I pulmonary adenocarcinoma. KEY POINTS: Significant findings of the study: The Psf3 expression could be a biomarker of adjuvant tegafur‐uracil administration for stage I pulmonary adenocarcinoma. What this study adds: Appropriate patients of adjuvant chemotherapy for stage I pulmonary adenocarcinoma using Psf3 expression could be selected. John Wiley & Sons Australia, Ltd 2019-10-22 2019-12 /pmc/articles/PMC6885426/ /pubmed/31637868 http://dx.doi.org/10.1111/1759-7714.13230 Text en © 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kimura, Kenji Tanaka, Yugo Tauchi, Shunsuke Kitamura, Yoshitaka Nishio, Wataru Sakai, Yasuhiro Hayashi, Yoshitake Yoshimura, Masahiro Maniwa, Yoshimasa Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
title | Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
title_full | Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
title_fullStr | Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
title_full_unstemmed | Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
title_short | Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
title_sort | psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885426/ https://www.ncbi.nlm.nih.gov/pubmed/31637868 http://dx.doi.org/10.1111/1759-7714.13230 |
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