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Volume 41, Issue 2, Pages 190-198 (February 2010)


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Highly concordant coexpression of aromatase and estrogen receptor β in non–small cell lung cancer

Keiko Abe, MD, PhDaCorresponding Author Informationemail address, Yasuhiro Miki, PhDa, Katsuhiko Ono, CTa, Miki Mori, CTa, Hideaki Kakinumaa, Yuki Koua, Nobutaka Kudoa, Masashi Koguchia, Hiromichi Niikawa, MD, PhDb, Satoshi Suzuki, MD, PhDc, Dean B. Evansd, Shunichi Sugawara, MDe, Takashi Suzuki, MD, PhDa, Hironobu Sasano, MD, PhDa

Received 14 May 2009; received in revised form 15 July 2009; accepted 17 July 2009. published online 05 October 2009.

Summary 

Estrogen receptor expression has been reported in non–small cell lung cancer. We examined the correlation between aromatase, a key enzyme in the synthesis of estrogen, and estrogen receptor expressions in 105 non–small cell lung cancer cases. All patients were older than 60 years, and all female patients were postmenopausal. Estrogen receptor α and progesterone receptor were detected in only 1 and 14 cases, respectively. Estrogen receptor β and aromatase were positive in 75 and 89 cases respectively. Estrogen receptor β expression in non–small cell lung cancer showed an inverse correlation with lymph node metastasis (P < .05). Only among females, both estrogen receptor β and aromatase expressions were correlated with higher Ki-67 labeling index and younger age (P < .05). Among 89 aromatase-positive cases, 70 were positive for estrogen receptor β, demonstrating a significant concordance (P < .05). Simultaneous immunohistochemical staining for aromatase and estrogen receptor β showed a high rate of double positive association. Male non–small cell lung cancer cases with double positivity for aromatase and estrogen receptor β demonstrated lower status in N factor by TNM classification (P < .05). In addition, among 89 aromatase-positive cases, a low-Allred total score of estrogen receptor β showed a significant relationship with large tumor size and high T factor by TNM classification (P < .05). In conclusion, frequent coexpression of aromatase and estrogen receptor β in non–small cell lung cancer might suggest some functional correlation between aromatase and estrogen receptor β, whereas estrogen receptor β negativity might be correlated with malignant progression of non–small cell lung cancer.

a Department of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan

b Department of Thoracic Surgery, Iwate Prefecture Central Hospital, Iwate, Japan

c Department of Thoracic Surgery, Ishinomaki Redcross Hospital, Ishinomaki, Japan

d Novartis, Institutes for BioMedical Research Basel, Oncology Research, Basel, Switzerland

e Department of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan

Corresponding Author InformationCorresponding author.

 This work was supported, in part, by a grant-in-aid for Scientific Research from the Ministry of Health and Welfare, and a grant-in-aid from the Ministry of Education, Science and Culture.

PII: S0046-8177(09)00260-3

doi:10.1016/j.humpath.2009.07.010


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