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Prostaglandin E-Major Urinary Metabolite (PGE-MUM) as a Tumor Marker for Lung Adenocarcinoma

Authors :
Mitsuo Hashimoto
Satoru Ito
Kazuyoshi Kuwano
Mutsunori Fujiwara
Yu Fujita
Hirofumi Utsumi
Hiromichi Hara
Jun Araya
Takanori Numata
Hironori Kawamoto
Seiji Arihiro
Shunsuke Minagawa
Tomokazu Matsuura
Hiroshi Wakui
Akihiro Ichikawa
Source :
Cancers, Volume 11, Issue 6, Cancers, Vol 11, Iss 6, p 768 (2019)
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

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 &mu<br />g/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.

Details

ISSN :
20726694
Volume :
11
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....5a3249f08af4ea16c7882110e67a0fb4
Full Text :
https://doi.org/10.3390/cancers11060768