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Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma
Background: Prostaglandin E2 (PGE2) is metabolized to prostaglandin E-major urinary metabolite (PGE-MUM). Enhanced cyclooxygenase-2 (COX-2) expression demonstrated in lung adenocarcinoma indicates increased PGE-MUM levels in patients with lung adenocarcinoma. Objectives: We aimed to elucidate the cl...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627988/ https://www.ncbi.nlm.nih.gov/pubmed/31163629 http://dx.doi.org/10.3390/cancers11060768 |
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author | Kawamoto, Hironori Hara, Hiromichi Araya, Jun Ichikawa, Akihiro Fujita, Yu Utsumi, Hirofumi Hashimoto, Mitsuo Wakui, Hiroshi Minagawa, Shunsuke Numata, Takanori Arihiro, Seiji Matsuura, Tomokazu Fujiwara, Mutsunori Ito, Satoru Kuwano, Kazuyoshi |
author_facet | Kawamoto, Hironori Hara, Hiromichi Araya, Jun Ichikawa, Akihiro Fujita, Yu Utsumi, Hirofumi Hashimoto, Mitsuo Wakui, Hiroshi Minagawa, Shunsuke Numata, Takanori Arihiro, Seiji Matsuura, Tomokazu Fujiwara, Mutsunori Ito, Satoru Kuwano, Kazuyoshi |
author_sort | Kawamoto, Hironori |
collection | PubMed |
description | Background: Prostaglandin E2 (PGE2) is metabolized to prostaglandin E-major urinary metabolite (PGE-MUM). Enhanced cyclooxygenase-2 (COX-2) expression demonstrated in lung adenocarcinoma indicates increased PGE-MUM levels in patients with lung adenocarcinoma. Objectives: We aimed to elucidate the clinical usefulness of measuring PGE-MUM as an indicator of tumor burden in patients with lung adenocarcinoma. Methods: PGE-MUM was measured by a radioimmunoassay in control healthy volunteers (n = 124) and patients with lung adenocarcinoma (n = 54). Associations between PGE-MUM levels and clinical characteristics of the patients (including lung cancer stage and TNM factors (T: Tumor, N: Node, M: Metastasis) were examined. Results: PGE-MUM levels were significantly elevated in patients with lung adenocarcinoma. A PGE-MUM level of 14.9 μg/g∙Cr showed 70.4% sensitivity and 67.7% specificity for the diagnosis of lung adenocarcinoma. PGE-MUM levels tended to be positively correlated with cancer progression as determined by the TNM staging system. Advanced stage (stage III, stage IV, and recurrence) was significantly associated with high PGE-MUM levels by logistic regression analysis. No apparent correlation was demonstrated between PGE-MUM and carcinoma embryonic antigen (CEA) levels. Conclusions: PGE-MUM can be a promising biomarker reflecting the systemic tumor burden of lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-6627988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66279882019-07-23 Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma Kawamoto, Hironori Hara, Hiromichi Araya, Jun Ichikawa, Akihiro Fujita, Yu Utsumi, Hirofumi Hashimoto, Mitsuo Wakui, Hiroshi Minagawa, Shunsuke Numata, Takanori Arihiro, Seiji Matsuura, Tomokazu Fujiwara, Mutsunori Ito, Satoru Kuwano, Kazuyoshi Cancers (Basel) Article Background: Prostaglandin E2 (PGE2) is metabolized to prostaglandin E-major urinary metabolite (PGE-MUM). Enhanced cyclooxygenase-2 (COX-2) expression demonstrated in lung adenocarcinoma indicates increased PGE-MUM levels in patients with lung adenocarcinoma. Objectives: We aimed to elucidate the clinical usefulness of measuring PGE-MUM as an indicator of tumor burden in patients with lung adenocarcinoma. Methods: PGE-MUM was measured by a radioimmunoassay in control healthy volunteers (n = 124) and patients with lung adenocarcinoma (n = 54). Associations between PGE-MUM levels and clinical characteristics of the patients (including lung cancer stage and TNM factors (T: Tumor, N: Node, M: Metastasis) were examined. Results: PGE-MUM levels were significantly elevated in patients with lung adenocarcinoma. A PGE-MUM level of 14.9 μg/g∙Cr showed 70.4% sensitivity and 67.7% specificity for the diagnosis of lung adenocarcinoma. PGE-MUM levels tended to be positively correlated with cancer progression as determined by the TNM staging system. Advanced stage (stage III, stage IV, and recurrence) was significantly associated with high PGE-MUM levels by logistic regression analysis. No apparent correlation was demonstrated between PGE-MUM and carcinoma embryonic antigen (CEA) levels. Conclusions: PGE-MUM can be a promising biomarker reflecting the systemic tumor burden of lung adenocarcinoma. MDPI 2019-06-03 /pmc/articles/PMC6627988/ /pubmed/31163629 http://dx.doi.org/10.3390/cancers11060768 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kawamoto, Hironori Hara, Hiromichi Araya, Jun Ichikawa, Akihiro Fujita, Yu Utsumi, Hirofumi Hashimoto, Mitsuo Wakui, Hiroshi Minagawa, Shunsuke Numata, Takanori Arihiro, Seiji Matsuura, Tomokazu Fujiwara, Mutsunori Ito, Satoru Kuwano, Kazuyoshi Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma |
title | Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma |
title_full | Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma |
title_fullStr | Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma |
title_full_unstemmed | Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma |
title_short | Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma |
title_sort | prostaglandin e-major urinary metabolite (pge-mum) as a tumor marker for lung adenocarcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627988/ https://www.ncbi.nlm.nih.gov/pubmed/31163629 http://dx.doi.org/10.3390/cancers11060768 |
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