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Endocrine-Related Cancer 15 (1) 113-124    DOI: 10.1677/ERC-07-0092
Copyright © 2008 by the Society for Endocrinology.
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Intratumoral concentration of sex steroids and expression of sex steroid-producing enzymes in ductal carcinoma in situ of human breast

Rie Shibuya, Takashi Suzuki, Yasuhiro Miki, Kimako Yoshida, Takuya Moriya, Katsuhiko Ono, Jun-ichi Akahira, Takanori Ishida1, Hisashi Hirakawa2, Dean B Evans3 and Hironobu Sasano

Department of Pathology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan1 Department of Surgery, Tohoku University School of Medicine, 980-575 Sendai, Japan2 Department of Surgery, Tohoku Kosai Hospital, 980-0803 Sendai, Japan3 Novartis Institutes for BioMedical Research Basel, Oncology Research, 4002 Basel, Switzerland

(Correspondence should be addressed to T Suzuki; Email: t-suzuki{at}patholo2.med.tohoku.ac.jp)

It is well known that sex steroids play important roles in the development of invasive ductal carcinoma (IDC) of the human breast. However, biological significance of sex steroids remains largely unclear in ductal carcinoma in situ (DCIS), regarded as a precursor lesion of IDC, which is partly due to the fact that the intratumoral concentration of sex steroids has not been examined in DCIS. Therefore, in this study, we first examined the intratumoral concentrations of estradiol and 5{alpha}-dihydrotestosterone (DHT) using liquid chromatography/electrospray tandem mass spectrometry in DCIS. Intratumoral concentrations of both estradiol and DHT were threefold higher in DCIS than non-neoplastic breast tissues and estrogen-producing enzymes (aromatase, steroid sulfatase, and 17β-hydroxysteroid dehydrogenase type 1 (17βHSD1)), and androgen-producing enzymes (17βHSD5 and 5{alpha}-reductase type 1 (5{alpha}Red1)) were abundantly expressed in DCIS by real-time PCR and immunohistochemical analyses. The intratumoral concentration of DHT was significantly lower in IDC than DCIS, while the expression of aromatase mRNA in carcinoma cells and intratumoral stromal cells was significantly higher in IDC than those in DCIS. Immunohistochemistry for sex steroid-producing enzymes in DCIS demonstrated that 5{alpha}Red1 immunoreactivity was positively correlated with Ki-67 labeling index and histological grade and was also associated with an increased risk of recurrence in patients with DCIS examined. Results of our study suggest that intratumoral concentrations of estradiol and DHT are increased in DCIS, which is possibly due to intratumoral production of these steroids. Therefore, estradiol and DHT may play important roles in the development of DCIS of the human breast.







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