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10.1245/s10434-006-9001-4
Annals of Surgical Oncology 13:1224-1234 (2006)
© 2006 Society of Surgical Oncology
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Original Article

Clinical Implications of Microsomal Prostaglandin E Synthase-1 Overexpression in Human Non–Small-Cell Lung Cancer

Hao-Wei Wang, MD1, Chung-Tsen Hsueh, MD, PhD2, Chien-Fu Jeff Lin, MD, PhD3, Teh-Ying Chou, MD, PhD4, Wen-Hu Hsu, MD1, Liang-Shun Wang, MD1 and Yu-Chung Wu, MD1

1 Division of Thoracic Surgery, Department of Surgery, Taipei Veterans General Hospital and School of Medicine, National Yang-Ming University, 201, Sec 2, Shih-Pai Road, Taipei 112, Taiwan
2 Division of Hematology/Oncology, Department of Internal Medicine, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA
3 Department of Statistics, National Taipei University, 151 University Road, San Shia, Taipei 237, Taiwan
4 Department of Pathology, Taipei Veterans General Hospital and School of Medicine, National Yang-Ming University, 201, Sec 2, Shih-pai Road, Taipei 112, Taiwan

Correspondence: Address correspondence and reprint requests to: Yu-Chung Wu, MD; E-mail: wuyc{at}vghtpe.gov.tw

Background: Microsomal prostaglandin E synthase-1 (mPGES-1) has recently been found to overexpress in human cancers, including non–small-cell lung cancer (NSCLC). However, the clinical value is largely unknown. The aim of this study was to investigate the associations between mPGES-1 expression in NSCLC and the clinical characteristics and survival outcome.

Methods: Between 2001 and 2003, paired fresh tumorous and nontumorous samples were prospectively procured from patients undergoing surgery for NSCLC. The expression of mPGES-1 was assessed by using Western blot in 93 subjects and reverse transcriptase-polymerase chain reaction in 35. Overexpression of mPGES-1 was defined as a more than 2-fold expression in the tumorous sample compared with the corresponding nontumorous one. Immunohistochemistry was used to confirm its localization to the tumor cells. In a subset of 30 cases, cyclooxygenase-2 (COX-2) was also analyzed to assess its association with mPGES-1.

Results: The protein and messenger RNA of mPGES-1 were both expressed at higher levels in the tumor samples (P < .001 and P = .006, respectively). The expressions of mPGES-1 and COX-2 were unrelated (P = .715). Overexpression of mPGES-1 protein was observed in 61 (65.6%) of 93 patients, but it was not significantly associated with the clinicopathologic characteristics or overall and disease-free survivals. However, mPGES-1 overexpression seemed to be associated with the likelihood of subsequent pulmonary metastases and a lower tendency for developing bony metastases (P = .001 and P = .006, respectively).

Conclusions: Our results demonstrated that mPGES-1 was overexpressed in NSCLC, unassociated with COX-2. Overexpression of mPGES-1 per se was not a prognostic indicator, but it might be implicated in the organ preference of metastasis.

Key Words: Non–small-cell lung cancer • Prostaglandin-endoperoxide synthase • Prostaglandins • Cyclooxygenase inhibitors







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