Estrogen Receptor α and β are Prognostic Factors in Non–Small Cell Lung Cancer

• Published in: Clinical cancer research Vol. 11; no. 14; pp. 5084 - 5089
• Main Authors: KAWAI, Hideki, ISHII, Akira, WASHIYA, Kiyotada, KONNO, Toshiko, KON, Hiroto, YAMAYA, Chiharu, ONO, Iwao, MINAMIYA, Yoshihiro, OGAWA, Junichi
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 15.07.2005
• Subjects: Adult; Aged; Aged, 80 and over; Antineoplastic agents; Biological and medical sciences; Biomarkers, Tumor - blood; Biomarkers, Tumor - genetics; Carcinoma, Non-Small-Cell Lung - genetics; Carcinoma, Non-Small-Cell Lung - pathology; estrogen receptor; Estrogen Receptor alpha - blood; Estrogen Receptor beta - blood; Female; Gene Expression Profiling; Humans; immunohistochemical staining; Immunohistochemistry; lung cancer; Lung Neoplasms - pathology; Male; Medical sciences; Middle Aged; Pharmacology. Drug treatments; Pneumology; Prognosis; prognostic factor; surgical specimen; Tumors of the respiratory system and mediastinum; Lung disease; Estrogen receptor α; Prognosis; Respiratory disease; Lung cancer; Bronchus disease; Malignant tumor; non-small cell lung carcinoma
• ISSN: 1078-0432; 1557-3265
• DOI: 10.1158/1078-0432.CCR-05-0200

Purpose: Estrogen receptor-α (ER-α) and -β (ER-β) play important roles in the carcinogenesis of breast tumors. Similarly, there have been several reports of ER expression in lung cancers, but the results have not been consistent, and the receptors' prognostic value remains unclear. Our goal was to investigate ER expression in non–small cell lung cancer (NSCLC) and to assess whether their expression correlates with prognosis. Experimental Design: ER expression was examined using immunohistochemical methods with sections from 132 resected NSCLC specimens. Kaplan-Meier survival curves were analyzed to determine the significance of ER expression in the prognosis of NSCLC patients. Results: ER-α was detected in the cytoplasm of 73% of the specimens analyzed, whereas ER-β was detected in the nucleus of 51%. ER-α expression correlated with poorer overall survival ( P <0.001), as did the absence of ER-β expression ( P = 0.048). Likewise, at histopathologic stage I, ER-α expression ( P = 0.028) or the absence of ER-β ( P = 0.037) correlated with a poorer prognosis, and ER-α(+)ER-β(−) patients had a significantly worse prognosis than ER-α(−)ER-β(+) patients ( P = 0.00007). Multivariate Cox regression analysis revealed the absence of ER-β to be an independent factor predictive of poor disease outcome (hazard ratio, 1.9; 95% confidence interval, 1.1-3.4; P = 0.0264). Conclusions: ER-α expression and the absence of ER-β expression are associated with a poorer prognosis among NSCLC patients. In particular, the absence of ER-β could serve as a marker identifying patients at high risk even at an early clinical stage.