Expression level of enzymes related to in situ estrogen synthesis and clinicopathological parameters in breast cancer patients

被引:28
作者
Suzuki, Masayo [1 ]
Ishida, Hiroyuki [1 ]
Shiotsu, Yukimasa [1 ]
Nakata, Taisuke [1 ]
Akinaga, Shiro [1 ]
Takashima, Shigemitsu [2 ]
Utsumi, Toshiaki [3 ]
Saeki, Toshiaki [4 ]
Harada, Nobuhiro [3 ]
机构
[1] Kyowa Hakko Kogyo Co Ltd, Pharmaceut Res Ctr, Nagaizumi, Shizuoka 4118731, Japan
[2] Shikoku Canc Ctr, Dept Surg, Matsuyama, Ehime 7910288, Japan
[3] Fujita Hlth Univ, Sch Med, Dept Surg & Biochem, Aichi 4701192, Japan
[4] Saitama Med Univ, Dept Breast Oncol, Saitama 3500495, Japan
关键词
Tumor; Gene expression (RT-PCR); Hormone; Steroid; Enzyme; (STS; EST; aromatase; 17; beta-HSD); Receptor; (ER; erbB2); STEROID SULFATASE EXPRESSION; ESTRADIOL; AROMATASE; CARCINOMA; SULFOTRANSFERASE; 17-BETA-HYDROXYSTEROID-DEHYDROGENASE; DEHYDROGENASE; RECURRENCE; ACTIVATION; RECEPTOR;
D O I
10.1016/j.jsbmb.2008.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to evaluate the importance of estrogen production in tumor and Surrounding tissues, we measured mRNA expression levels of 5 enzymes participating to estrogen synthesis in situ and 4 breast cancer-related proteins in 27 pairs of tumor and non-malignant tissues. Steroid sulfatase (STS) mRNA was more frequently detected in tumor tissues rather than in their non-malignant counterparts. Estrogen sulfotransferase (EST) was constantly expressed with high level not only in tumor tissues but also in their surrounding non-malignant counterparts. In contrast, mRNA expression levels of aromatase, and 17 beta-hydroxysteroid dehydrogenase type I and II were relatively low and detected only in small proportion of the patients. We also measured the mRNA expression levels of the same nine genes in tumor tissues of 197 breast cancer patients, and analyzed relationship between the mRNA expression level and the clinicopathological parameters. The mRNA expression levels of STS, aromatase and erbB2 in tumor tissues increased as breast cancer progressed. The tumoral mRNA expression levels of STS. estrogen receptor P, and erbB2 in patients with recurrence were higher than those in patients without recurrence. Upregulation of STS expression plays an important role in tumor progression of human breast cancer and is considered to be responsible for estrogen production in tumor and surrounding tissues. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:195 / 201
页数:7
相关论文
共 26 条
  • [1] ADAMS JB, 1979, CANCER RES, V39, P5124
  • [2] Altucci L, 1996, ONCOGENE, V12, P2315
  • [3] INTRATUMORAL ESTRONE SULFATASE ACTIVITY AS A PROGNOSTIC MARKER IN HUMAN BREAST-CARCINOMA
    EVANS, TRJ
    ROWLANDS, MG
    LAW, M
    COOMBES, RC
    [J]. BRITISH JOURNAL OF CANCER, 1994, 69 (03) : 555 - 561
  • [4] Gunnarsson C, 2001, CANCER RES, V61, P8448
  • [5] THE BIOLOGY OF ERBB-2 NEU HER-2 AND ITS ROLE IN CANCER
    HYNES, NE
    STERN, DF
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1994, 1198 (2-3): : 165 - 184
  • [6] Genetic variants of CYP19 (aromatase) and breast cancer risk
    Kristensen, VN
    Harada, N
    Yoshimura, N
    Haraldsen, E
    Lonning, P
    Erikstein, B
    Kåresen, R
    Kristensen, T
    Borresen-Dale, AL
    [J]. ONCOGENE, 2000, 19 (10) : 1329 - 1333
  • [7] Adrenal androgens and intracrinology
    Labrie, F
    [J]. SEMINARS IN REPRODUCTIVE MEDICINE, 2004, 22 (04) : 299 - 309
  • [8] STRUCTURE, REGULATION AND ROLE OF 3-BETA-HYDROXYSTEROID DEHYDROGENASE, 17-BETA-HYDROXYSTEROID DEHYDROGENASE AND AROMATASE ENZYMES IN THE FORMATION OF SEX STEROIDS IN CLASSICAL AND PERIPHERAL INTRACRINE TISSUES
    LABRIE, F
    SIMARD, J
    LUUTHE, V
    PELLETIER, G
    BELGHMI, K
    BELANGER, A
    [J]. BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1994, 8 (02): : 451 - 474
  • [9] Pasqualini JR, 1996, J ENDOCRINOL, V150, pS99
  • [10] Concentrations of estrone, estradiol, and estrone sulfate and evaluation of sulfatase and aromatase activities in pre- and postmenopausal breast cancer patients
    Pasqualini, JR
    Chetrite, G
    Blacker, C
    Feinstein, MC
    Delalonde, L
    Talbi, M
    Maloche, C
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (04) : 1460 - 1464