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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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