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Erschienen in: Breast Cancer 4/2008

01.10.2008 | Special Feature

Intratumoral estrogen production in breast carcinoma: significance of aromatase

verfasst von: Takashi Suzuki, Yasuhiro Miki, Noriaki Ohuchi, Hironobu Sasano

Erschienen in: Breast Cancer | Ausgabe 4/2008

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Abstract

It is well known that estrogens are closely involved in the growth of human breast carcinoma, and that the great majority of breast carcinomas express estrogen receptor. Recent studies have demonstrated that estrogens are locally produced in breast carcinoma by several enzymes. Among these, aromatase is generally considered the most important enzyme, and aromatase inhibitors are currently used in the treatment of breast carcinoma in postmenopausal women as an estrogen deprivation therapy. Therefore, in this review, we summarize the results of recent studies on aromatase in breast carcinoma, and we discuss its biological and/or clinical significance. Aromatase was expressed in various cell types in breast carcinoma, such as carcinoma cells, intratumoral stromal cells and adipocytes adjacent to the carcinoma, and the aromatase expression was regulated by various factors, including carcinoma cell–stromal cell interactions, cytokines and nuclear receptors, depending on the cell types. Aromatase was involved not only in local estrogen production but also the inhibition of intratumoral androgen synthesis in breast carcinoma. Finally, tissue concentrations of sex steroids were significantly higher in noninvasive breast carcinoma, regarded as a precursor lesion to invasive carcinoma, than in non-neoplastic breast tissue, and various sex steroid-producing enzymes (including aromatase) were abundantly expressed in noninvasive breast carcinoma tissue. Therefore, sex steroids are locally produced in noninvasive breast carcinoma as well as invasive carcinoma, and endocrine therapies may be clinically effective in a select group of noninvasive breast carcinoma patients.
Literatur
1.
Zurück zum Zitat Sasano H, Suzuki T, Nakata T, Moriya T. New development in intracrinology of breast carcinoma. Breast Cancer. 2006;13:129–36.PubMedCrossRef Sasano H, Suzuki T, Nakata T, Moriya T. New development in intracrinology of breast carcinoma. Breast Cancer. 2006;13:129–36.PubMedCrossRef
2.
Zurück zum Zitat Chetrite GS, Cortes-Prieto J, Philippe JC, Wright F, Pasqualini JR. Comparison of estrogen concentrations, estrone sulfatase and aromatase activities in normal, and in cancerous, human breast tissues. J Steroid Biochem Mol Biol. 2000;72:23–7.PubMedCrossRef Chetrite GS, Cortes-Prieto J, Philippe JC, Wright F, Pasqualini JR. Comparison of estrogen concentrations, estrone sulfatase and aromatase activities in normal, and in cancerous, human breast tissues. J Steroid Biochem Mol Biol. 2000;72:23–7.PubMedCrossRef
3.
Zurück zum Zitat Miyoshi Y, Ando A, Shiba E, Taguchi T, Tamaki Y, Noguchi S. Involvement of up-regulation of 17β-hydroxysteroid dehydrogenase type 1 in maintenance of intratumoral high estradiol levels in postmenopausal breast cancers. Int J Cancer. 2001;94:685–9.PubMedCrossRef Miyoshi Y, Ando A, Shiba E, Taguchi T, Tamaki Y, Noguchi S. Involvement of up-regulation of 17β-hydroxysteroid dehydrogenase type 1 in maintenance of intratumoral high estradiol levels in postmenopausal breast cancers. Int J Cancer. 2001;94:685–9.PubMedCrossRef
4.
Zurück zum Zitat Labrie F, Luu-The V, Labrie C, Belanger A, Simard J, Lin SX, et al. Endocrine and intracrine sources of androgens in women: inhibition of breast cancer and other roles of androgens and their precursor dehydroepiandrosterone. Endocr Rev. 2003;24:152–82.PubMedCrossRef Labrie F, Luu-The V, Labrie C, Belanger A, Simard J, Lin SX, et al. Endocrine and intracrine sources of androgens in women: inhibition of breast cancer and other roles of androgens and their precursor dehydroepiandrosterone. Endocr Rev. 2003;24:152–82.PubMedCrossRef
5.
Zurück zum Zitat Miller WR, Dixon JM. Endocrine and clinical endpoints of exemestane as neoadjuvant therapy. Cancer Control. 2002;9:9–15.PubMed Miller WR, Dixon JM. Endocrine and clinical endpoints of exemestane as neoadjuvant therapy. Cancer Control. 2002;9:9–15.PubMed
6.
Zurück zum Zitat Geisler J, Lonning PE. Endocrine effects of aromatase inhibitors and inactivators in vivo: review of data and method limitations. J Steroid Biochem Mol Biol. 2005;95:75–81.PubMedCrossRef Geisler J, Lonning PE. Endocrine effects of aromatase inhibitors and inactivators in vivo: review of data and method limitations. J Steroid Biochem Mol Biol. 2005;95:75–81.PubMedCrossRef
7.
Zurück zum Zitat Geisler J. Breast cancer tissue estrogens and their manipulation with aromatase inhibitors and inactivators. J Steroid Biochem Mol Biol. 2003;86:245–53.PubMedCrossRef Geisler J. Breast cancer tissue estrogens and their manipulation with aromatase inhibitors and inactivators. J Steroid Biochem Mol Biol. 2003;86:245–53.PubMedCrossRef
8.
Zurück zum Zitat Baum M. Current status of aromatase inhibitors in the management of breast cancer and critique of the NCIC MA-17 trial. Cancer Control. 2004;11:217–21.PubMed Baum M. Current status of aromatase inhibitors in the management of breast cancer and critique of the NCIC MA-17 trial. Cancer Control. 2004;11:217–21.PubMed
9.
Zurück zum Zitat Coombes RC, Hall E, Gibson LJ, Paridaens R, Jassem J, Delozier T, et al. A randomized trial of exemestane after two to three years of tamoxifen therapy in postmenopausal women with primary breast cancer. N Engl J Med. 2004;350:1081–92.PubMedCrossRef Coombes RC, Hall E, Gibson LJ, Paridaens R, Jassem J, Delozier T, et al. A randomized trial of exemestane after two to three years of tamoxifen therapy in postmenopausal women with primary breast cancer. N Engl J Med. 2004;350:1081–92.PubMedCrossRef
10.
Zurück zum Zitat Howell A, Cuzick J, Baum M, Buzdar A, Dowsett M, Forbes JF, et al. Results of the ATAC (Arimidex, Tamoxifen, alone or in combination) trial after completion of 5 years’ adjuvant treatment for breast cancer. Lancet. 2005;365:60–2.PubMedCrossRef Howell A, Cuzick J, Baum M, Buzdar A, Dowsett M, Forbes JF, et al. Results of the ATAC (Arimidex, Tamoxifen, alone or in combination) trial after completion of 5 years’ adjuvant treatment for breast cancer. Lancet. 2005;365:60–2.PubMedCrossRef
11.
Zurück zum Zitat Utsumi T, Kobayashi N, Hanada H. Recent perspectives of endocrine therapy for breast cancer. Breast Cancer. 2007;14:194–9.PubMedCrossRef Utsumi T, Kobayashi N, Hanada H. Recent perspectives of endocrine therapy for breast cancer. Breast Cancer. 2007;14:194–9.PubMedCrossRef
12.
Zurück zum Zitat Suzuki T, Miki Y, Nakamura Y, Moriya T, Ito K, Ohuchi N, et al. Sex steroid-producing enzymes in human breast cancer. Endocr Relat Cancer. 2005;12:701–20.PubMedCrossRef Suzuki T, Miki Y, Nakamura Y, Moriya T, Ito K, Ohuchi N, et al. Sex steroid-producing enzymes in human breast cancer. Endocr Relat Cancer. 2005;12:701–20.PubMedCrossRef
13.
Zurück zum Zitat Utsumi T, Harada N, Maruta M, Takagi Y. Presence of alternatively spliced transcripts of aromatase gene in human breast cancer. J Clin Endocrinol Metab. 1996;81:2344–9.PubMedCrossRef Utsumi T, Harada N, Maruta M, Takagi Y. Presence of alternatively spliced transcripts of aromatase gene in human breast cancer. J Clin Endocrinol Metab. 1996;81:2344–9.PubMedCrossRef
14.
Zurück zum Zitat Sasano H, Nagura H, Harada N, Goukon Y, Kimura M. Immunolocalization of aromatase and other steroidogenic enzymes in human breast disorders. Hum Pathol. 1994;5:530–3.CrossRef Sasano H, Nagura H, Harada N, Goukon Y, Kimura M. Immunolocalization of aromatase and other steroidogenic enzymes in human breast disorders. Hum Pathol. 1994;5:530–3.CrossRef
15.
Zurück zum Zitat Santen RJ, Martel J, Hoagland M, Naftolin F, Roa L, Harada N, et al. Stromal spindle cells contain aromatase in human breast tumors. J Clin Endocrinol Metab. 1994;79:627–32.PubMedCrossRef Santen RJ, Martel J, Hoagland M, Naftolin F, Roa L, Harada N, et al. Stromal spindle cells contain aromatase in human breast tumors. J Clin Endocrinol Metab. 1994;79:627–32.PubMedCrossRef
16.
Zurück zum Zitat Esteban JM, Warsi Z, Haniu M, Hall P, Shively JE, Chen S. Detection of intratumoral aromatase in breast carcinomas. An immunohistochemical study with clinicopathologic correlation. Am J Pathol. 1992;140:337–43.PubMed Esteban JM, Warsi Z, Haniu M, Hall P, Shively JE, Chen S. Detection of intratumoral aromatase in breast carcinomas. An immunohistochemical study with clinicopathologic correlation. Am J Pathol. 1992;140:337–43.PubMed
17.
Zurück zum Zitat Brodie AM, Lu Q, Long BJ, Fulton A, Chen T, Macpherson N, et al. Aromatase and COX-2 expression in human breast cancers. J Steroid Biochem Mol Biol. 2001;79:41–7.PubMedCrossRef Brodie AM, Lu Q, Long BJ, Fulton A, Chen T, Macpherson N, et al. Aromatase and COX-2 expression in human breast cancers. J Steroid Biochem Mol Biol. 2001;79:41–7.PubMedCrossRef
18.
Zurück zum Zitat Sasano H, Anderson TJ, Silverberg SG, Santen RJ, Conway M, Edwards DP, et al. The validation of new aromatase monoclonal antibodies for immunohistochemistry—a correlation with biochemical activities in 46 cases of breast cancer. J Steroid Biochem Mol Biol. 2005;95:35–9.PubMedCrossRef Sasano H, Anderson TJ, Silverberg SG, Santen RJ, Conway M, Edwards DP, et al. The validation of new aromatase monoclonal antibodies for immunohistochemistry—a correlation with biochemical activities in 46 cases of breast cancer. J Steroid Biochem Mol Biol. 2005;95:35–9.PubMedCrossRef
19.
Zurück zum Zitat Shibuya R, Suzuki T, Miki Y, Yoshida K, Moriya T, Katsuhiko Ono K, et al. Intratumoral concentration of sex steroids and expression of sex steroid-producing enzymes in ductal carcinoma in situ of human breast. Endocr Relat Cancer. 2008;15:113–24.PubMedCrossRef Shibuya R, Suzuki T, Miki Y, Yoshida K, Moriya T, Katsuhiko Ono K, et al. Intratumoral concentration of sex steroids and expression of sex steroid-producing enzymes in ductal carcinoma in situ of human breast. Endocr Relat Cancer. 2008;15:113–24.PubMedCrossRef
20.
Zurück zum Zitat Miki Y, Suzuki T, Tazawa C, Yamaguchi Y, Kitada K, Honma S, et al. Aromatase localization in human breast cancer tissues: possible interactions between intratumoral stromal and parenchymal cells. Cancer Res. 2007;67:3945–54.PubMedCrossRef Miki Y, Suzuki T, Tazawa C, Yamaguchi Y, Kitada K, Honma S, et al. Aromatase localization in human breast cancer tissues: possible interactions between intratumoral stromal and parenchymal cells. Cancer Res. 2007;67:3945–54.PubMedCrossRef
21.
Zurück zum Zitat Reed MJ, Purohit A, Woo LW, Newman SP, Potter BV. Steroid sulfatase: molecular biology, regulation, and inhibition. Endocr Rev. 2005;26:171–202.PubMedCrossRef Reed MJ, Purohit A, Woo LW, Newman SP, Potter BV. Steroid sulfatase: molecular biology, regulation, and inhibition. Endocr Rev. 2005;26:171–202.PubMedCrossRef
22.
Zurück zum Zitat Yamaguchi Y. Microenvironmental regulation of estrogen signals in breast cancer. Breast Cancer. 2007;14:175–81.PubMedCrossRef Yamaguchi Y. Microenvironmental regulation of estrogen signals in breast cancer. Breast Cancer. 2007;14:175–81.PubMedCrossRef
23.
Zurück zum Zitat Clyne CD, Speed CJ, Zhou J, Simpson ER. Liver receptor homologue-1 (LRH-1) regulates expression of aromatase in preadipocytes. J Biol Chem. 2002;277:20591–7.PubMedCrossRef Clyne CD, Speed CJ, Zhou J, Simpson ER. Liver receptor homologue-1 (LRH-1) regulates expression of aromatase in preadipocytes. J Biol Chem. 2002;277:20591–7.PubMedCrossRef
24.
Zurück zum Zitat Zhou J, Suzuki T, Kovacic A, Saito R, Miki Y, Ishida T, et al. Interactions between prostaglandin E(2), liver receptor homologue-1, and aromatase in breast cancer. Cancer Res. 2005;65:657–63.PubMed Zhou J, Suzuki T, Kovacic A, Saito R, Miki Y, Ishida T, et al. Interactions between prostaglandin E(2), liver receptor homologue-1, and aromatase in breast cancer. Cancer Res. 2005;65:657–63.PubMed
25.
Zurück zum Zitat Miki Y, Clyne CD, Suzuki T, Moriya T, Nakamura Y, Ishida T, et al. Immunolocalization of liver receptor homologue-1 (LRH-1) in human breast carcinoma: possible regulator of in situ steroidogenesis. Cancer Lett. 2006;244:24–33.PubMedCrossRef Miki Y, Clyne CD, Suzuki T, Moriya T, Nakamura Y, Ishida T, et al. Immunolocalization of liver receptor homologue-1 (LRH-1) in human breast carcinoma: possible regulator of in situ steroidogenesis. Cancer Lett. 2006;244:24–33.PubMedCrossRef
26.
Zurück zum Zitat Yang C, Zhou D, Chen S. Modulation of aromatase expression in the breast tissue by ERR α-1 orphan receptor. Cancer Res. 1998;58:5695–700.PubMed Yang C, Zhou D, Chen S. Modulation of aromatase expression in the breast tissue by ERR α-1 orphan receptor. Cancer Res. 1998;58:5695–700.PubMed
27.
Zurück zum Zitat Suzuki T, Miki Y, Moriya T, Shimada N, Ishida T, Hirakawa H, et al. Estrogen-related receptor α in human breast carcinoma as a potent prognostic factor. Cancer Res. 2004;64:4670–6.PubMedCrossRef Suzuki T, Miki Y, Moriya T, Shimada N, Ishida T, Hirakawa H, et al. Estrogen-related receptor α in human breast carcinoma as a potent prognostic factor. Cancer Res. 2004;64:4670–6.PubMedCrossRef
28.
Zurück zum Zitat Pasqualini JR. The selective estrogen enzyme modulators in breast cancer: a review. Biochim Biophys Acta. 2004;1654:123–43.PubMed Pasqualini JR. The selective estrogen enzyme modulators in breast cancer: a review. Biochim Biophys Acta. 2004;1654:123–43.PubMed
29.
Zurück zum Zitat Saeki T, Takashima S, Sasaki H, Hanai N, Salomon DS. Localization of estrone sulfatase in human breast carcinomas. Breast Cancer. 1999;6:331–7.PubMedCrossRef Saeki T, Takashima S, Sasaki H, Hanai N, Salomon DS. Localization of estrone sulfatase in human breast carcinomas. Breast Cancer. 1999;6:331–7.PubMedCrossRef
30.
Zurück zum Zitat Suzuki T, Nakata T, Miki Y, Kaneko C, Moriya T, Ishida T, et al. Estrogen sulfotransferase and steroid sulfatase in human breast carcinoma. Cancer Res. 2003;63:2762–70.PubMed Suzuki T, Nakata T, Miki Y, Kaneko C, Moriya T, Ishida T, et al. Estrogen sulfotransferase and steroid sulfatase in human breast carcinoma. Cancer Res. 2003;63:2762–70.PubMed
31.
Zurück zum Zitat Utsumi T, Yoshimura N, Takeuchi S, Ando J, Maruta M, Maeda K, et al. Steroid sulfatase expression is an independent predictor of recurrence in human breast cancer. Cancer Res. 1999;59:377–81.PubMed Utsumi T, Yoshimura N, Takeuchi S, Ando J, Maruta M, Maeda K, et al. Steroid sulfatase expression is an independent predictor of recurrence in human breast cancer. Cancer Res. 1999;59:377–81.PubMed
32.
Zurück zum Zitat Miyoshi Y, Ando A, Hasegawa S, Ishitobi M, Taguchi T, Tamaki Y, et al. High expression of steroid sulfatase mRNA predicts poor prognosis in patients with estrogen receptor-positive breast cancer. Clin Cancer Res. 2003;9:2288–93.PubMed Miyoshi Y, Ando A, Hasegawa S, Ishitobi M, Taguchi T, Tamaki Y, et al. High expression of steroid sulfatase mRNA predicts poor prognosis in patients with estrogen receptor-positive breast cancer. Clin Cancer Res. 2003;9:2288–93.PubMed
33.
Zurück zum Zitat Stanway SJ, Purohit A, Woo LW, Sufi S, Vigushin D, Ward R, et al. Phase I study of STX 64 (667 Coumate) in breast cancer patients: the first study of a steroid sulfatase inhibitor. Clin Cancer Res. 2006;12:1585–9.PubMedCrossRef Stanway SJ, Purohit A, Woo LW, Sufi S, Vigushin D, Ward R, et al. Phase I study of STX 64 (667 Coumate) in breast cancer patients: the first study of a steroid sulfatase inhibitor. Clin Cancer Res. 2006;12:1585–9.PubMedCrossRef
34.
Zurück zum Zitat Horiguchi Y, Araki M, Motojima K. 17beta-Hydroxysteroid dehydrogenase type 13 is a liver-specific lipid droplet-associated protein. Biochem Biophys Res Commun. 2008;370:235–8.PubMedCrossRef Horiguchi Y, Araki M, Motojima K. 17beta-Hydroxysteroid dehydrogenase type 13 is a liver-specific lipid droplet-associated protein. Biochem Biophys Res Commun. 2008;370:235–8.PubMedCrossRef
35.
Zurück zum Zitat Suzuki T, Moriya T, Ariga N, Kaneko C, Kanazawa M, Sasano H. 17β-hydroxysteroid dehydrogenase type 1 and type 2 in human breast carcinoma: a correlation to clinicopathological parameters. Br J Cancer. 2000;82:518–23.PubMedCrossRef Suzuki T, Moriya T, Ariga N, Kaneko C, Kanazawa M, Sasano H. 17β-hydroxysteroid dehydrogenase type 1 and type 2 in human breast carcinoma: a correlation to clinicopathological parameters. Br J Cancer. 2000;82:518–23.PubMedCrossRef
36.
Zurück zum Zitat Gunnarsson C, Olsson BM, Stal O, Southeast Sweden Breast Cancer Group. Abnormal expression of 17β-hydroxysteroid dehydrogenases in breast cancer predicts late recurrence. Cancer Res. 2001;61:8448–51.PubMed Gunnarsson C, Olsson BM, Stal O, Southeast Sweden Breast Cancer Group. Abnormal expression of 17β-hydroxysteroid dehydrogenases in breast cancer predicts late recurrence. Cancer Res. 2001;61:8448–51.PubMed
37.
Zurück zum Zitat Mistry P, Griffiths K, Maynard PV. Endogenous C19-steroids and oestradiol levels in human primary breast tumour tissues and their correlation with androgen and oestrogen receptors. J Steroid Biochem. 1986;24:1117–25.PubMedCrossRef Mistry P, Griffiths K, Maynard PV. Endogenous C19-steroids and oestradiol levels in human primary breast tumour tissues and their correlation with androgen and oestrogen receptors. J Steroid Biochem. 1986;24:1117–25.PubMedCrossRef
38.
Zurück zum Zitat Recchione C, Venturelli E, Manzari A, Cavalleri A, Martinetti A, Secreto G. Testosterone, dihydrotestosterone and oestradiol levels in postmenopausal breast cancer tissues. J Steroid Biochem Mol Biol. 1995;52:541–6.PubMedCrossRef Recchione C, Venturelli E, Manzari A, Cavalleri A, Martinetti A, Secreto G. Testosterone, dihydrotestosterone and oestradiol levels in postmenopausal breast cancer tissues. J Steroid Biochem Mol Biol. 1995;52:541–6.PubMedCrossRef
39.
Zurück zum Zitat Suzuki T, Miki Y, Moriya T, Akahira J, Ishida T, Hirakawa H, et al. 5α-reductase type 1 and aromatase in breast carcinoma as regulators of in situ androgen production. Int J Cancer. 2007;20:285–91.CrossRef Suzuki T, Miki Y, Moriya T, Akahira J, Ishida T, Hirakawa H, et al. 5α-reductase type 1 and aromatase in breast carcinoma as regulators of in situ androgen production. Int J Cancer. 2007;20:285–91.CrossRef
40.
Zurück zum Zitat Isola JJ. Immunohistochemical demonstration of androgen receptor in breast cancer and its relationship to other prognostic factors. J Pathol. 1993;170:31–5.PubMedCrossRef Isola JJ. Immunohistochemical demonstration of androgen receptor in breast cancer and its relationship to other prognostic factors. J Pathol. 1993;170:31–5.PubMedCrossRef
41.
Zurück zum Zitat Suzuki T, Darnel AD, Akahira JI, Ariga N, Ogawa S, Kaneko C, et al. 5α-reductases in human breast carcinoma: possible modulator of in situ androgenic actions. J Clin Endocrinol Metab. 2001;86:2250–7.PubMedCrossRef Suzuki T, Darnel AD, Akahira JI, Ariga N, Ogawa S, Kaneko C, et al. 5α-reductases in human breast carcinoma: possible modulator of in situ androgenic actions. J Clin Endocrinol Metab. 2001;86:2250–7.PubMedCrossRef
42.
Zurück zum Zitat Moinfar F, Okcu M, Tsybrovskyy O, Regitnig P, Lax SF, Weybora W, et al. Androgen receptors frequently are expressed in breast carcinomas: potential relevance to new therapeutic strategies. Cancer. 2003;98:703–11.PubMedCrossRef Moinfar F, Okcu M, Tsybrovskyy O, Regitnig P, Lax SF, Weybora W, et al. Androgen receptors frequently are expressed in breast carcinomas: potential relevance to new therapeutic strategies. Cancer. 2003;98:703–11.PubMedCrossRef
43.
Zurück zum Zitat Spinola PG, Marchetti B, Merand Y, Belanger A, Labrie F. Effects of the aromatase inhibitor 4-hydroxyandrostenedione and the antiandrogen flutamide on growth and steroid levels in DMBA-induced rat mammary tumors. Breast Cancer Res Treat. 1988;12:287–96.PubMedCrossRef Spinola PG, Marchetti B, Merand Y, Belanger A, Labrie F. Effects of the aromatase inhibitor 4-hydroxyandrostenedione and the antiandrogen flutamide on growth and steroid levels in DMBA-induced rat mammary tumors. Breast Cancer Res Treat. 1988;12:287–96.PubMedCrossRef
44.
Zurück zum Zitat Sonne-Hansen K, Lykkesfeldt AE. Endogenous aromatization of testosterone results in growth stimulation of the human MCF-7 breast cancer cell line. J Steroid Biochem Mol Biol. 2005;93:25–34.PubMedCrossRef Sonne-Hansen K, Lykkesfeldt AE. Endogenous aromatization of testosterone results in growth stimulation of the human MCF-7 breast cancer cell line. J Steroid Biochem Mol Biol. 2005;93:25–34.PubMedCrossRef
45.
Zurück zum Zitat Franceschi S, Levi F, La VC, Randimbison L, Te VC. Second cancers following in situ carcinoma of the breast. Int J Cancer. 1998;77:392–5.PubMedCrossRef Franceschi S, Levi F, La VC, Randimbison L, Te VC. Second cancers following in situ carcinoma of the breast. Int J Cancer. 1998;77:392–5.PubMedCrossRef
46.
Zurück zum Zitat Warnberg F, Yuen J, Holmberg L. Risk of subsequent invasive breast cancer after breast carcinoma in situ. Lancet. 2000;355:724–5.PubMedCrossRef Warnberg F, Yuen J, Holmberg L. Risk of subsequent invasive breast cancer after breast carcinoma in situ. Lancet. 2000;355:724–5.PubMedCrossRef
47.
Zurück zum Zitat Kusama R, Takayama F, Tsuchiya S. MRI of the breast: comparison of MRI signals and histological characteristics of the same slices. Med Mol Morphol. 2005;38:204–15.PubMedCrossRef Kusama R, Takayama F, Tsuchiya S. MRI of the breast: comparison of MRI signals and histological characteristics of the same slices. Med Mol Morphol. 2005;38:204–15.PubMedCrossRef
48.
Zurück zum Zitat Li CI, Daling JR, Malone KE. Age specific incidence rates of in situ breast carcinomas by histologic type, 1980 to 2001. Cancer Epidemiol Biomarkers Prev. 2005;14:1008–11.PubMedCrossRef Li CI, Daling JR, Malone KE. Age specific incidence rates of in situ breast carcinomas by histologic type, 1980 to 2001. Cancer Epidemiol Biomarkers Prev. 2005;14:1008–11.PubMedCrossRef
49.
Zurück zum Zitat Moriya T, Hirakawa H, Suzuki T, Sasano H, Ohuchi N. Ductal carcinoma in situ and related lesions of the breast: recent advances in pathology practice. Breast Cancer. 2004;11:325–33. Moriya T, Hirakawa H, Suzuki T, Sasano H, Ohuchi N. Ductal carcinoma in situ and related lesions of the breast: recent advances in pathology practice. Breast Cancer. 2004;11:325–33.
50.
Zurück zum Zitat Kepple J, Henry-Tillman RS, Klimberg VS, Layeeque R, Siegel E, Westbrook K, et al. The receptor expression pattern in ductal carcinoma in situ predicts recurrence. Am J Surg. 2006;192:68–71.PubMedCrossRef Kepple J, Henry-Tillman RS, Klimberg VS, Layeeque R, Siegel E, Westbrook K, et al. The receptor expression pattern in ductal carcinoma in situ predicts recurrence. Am J Surg. 2006;192:68–71.PubMedCrossRef
51.
Zurück zum Zitat Tsikitis VL, Chung MA. Biology of ductal carcinoma in situ classification based on biologic potential. Am J Clin Oncol. 2006;29:305–10.PubMedCrossRef Tsikitis VL, Chung MA. Biology of ductal carcinoma in situ classification based on biologic potential. Am J Clin Oncol. 2006;29:305–10.PubMedCrossRef
52.
Zurück zum Zitat Selim AG, El-Ayat G, Wells CA. Androgen receptor expression in ductal carcinoma in situ of the breast: relation to oestrogen and progesterone receptors. J Clin Pathol. 2002;55:14–6.PubMed Selim AG, El-Ayat G, Wells CA. Androgen receptor expression in ductal carcinoma in situ of the breast: relation to oestrogen and progesterone receptors. J Clin Pathol. 2002;55:14–6.PubMed
53.
Zurück zum Zitat Barnes NL, Boland GP, Davenport A, Knox WF, Bundred NJ. Relationship between hormone receptor status and tumour size, grade and comedo necrosis in ductal carcinoma in situ. Br J Surg. 2005;92:429–34.PubMedCrossRef Barnes NL, Boland GP, Davenport A, Knox WF, Bundred NJ. Relationship between hormone receptor status and tumour size, grade and comedo necrosis in ductal carcinoma in situ. Br J Surg. 2005;92:429–34.PubMedCrossRef
54.
Zurück zum Zitat Rody A, Diallo R, Poremba C, Wuelfing P, Kissler S, Solbach C, et al. Androgen receptor expression in ductal carcinoma in situ of the breast: not a helpful marker for classification such as estrogen receptor alpha and progesterone receptor. Appl Immunohistochem Mol Morphol. 2005;13:25–9.PubMedCrossRef Rody A, Diallo R, Poremba C, Wuelfing P, Kissler S, Solbach C, et al. Androgen receptor expression in ductal carcinoma in situ of the breast: not a helpful marker for classification such as estrogen receptor alpha and progesterone receptor. Appl Immunohistochem Mol Morphol. 2005;13:25–9.PubMedCrossRef
55.
Zurück zum Zitat Namba R, Young LJ, Maglione JE, McGoldrick ET, Liu S, Wurz GT, et al. Selective estrogen receptor modulators inhibit growth and progression of premalignant lesions in a mouse model of ductal carcinoma in situ. Breast Cancer Res. 2005;7:R881–9.PubMedCrossRef Namba R, Young LJ, Maglione JE, McGoldrick ET, Liu S, Wurz GT, et al. Selective estrogen receptor modulators inhibit growth and progression of premalignant lesions in a mouse model of ductal carcinoma in situ. Breast Cancer Res. 2005;7:R881–9.PubMedCrossRef
56.
Zurück zum Zitat Dunn BK, Wickerham DL, Ford LG. Prevention of hormone-related cancers: breast cancer. J Clin Oncol. 2005;23:357–67.PubMedCrossRef Dunn BK, Wickerham DL, Ford LG. Prevention of hormone-related cancers: breast cancer. J Clin Oncol. 2005;23:357–67.PubMedCrossRef
57.
Metadaten
Titel
Intratumoral estrogen production in breast carcinoma: significance of aromatase
verfasst von
Takashi Suzuki
Yasuhiro Miki
Noriaki Ohuchi
Hironobu Sasano
Publikationsdatum
01.10.2008
Verlag
Springer Japan
Erschienen in
Breast Cancer / Ausgabe 4/2008
Print ISSN: 1340-6868
Elektronische ISSN: 1880-4233
DOI
https://doi.org/10.1007/s12282-008-0062-z

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