4.6 Article

Tamoxifen inhibits transforming growth factor-α gene expression in human breast carcinoma samples treated with triiodothyronine

Journal

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
Volume 31, Issue 12, Pages 1047-1051

Publisher

SPRINGER
DOI: 10.1007/BF03345650

Keywords

Breast cancer samples; estrogen; tamoxifen; TGF-alpha; triiodothyronine

Funding

  1. FAPESP [04/12338-7, 05/55459-1]

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Objectives: To examine the effects of triiodothyronine (T-3), 17 beta-estradiol (E-2), and tamoxifen (TAM) on transforming growth factor (TGF)-alpha gene expression in primary breast cancer cell cultures and interactions between the different treatments. Methods and results: Patients included in the study (no.=12) had been newly diagnosed with breast cancer. Fresh human breast carcinoma tissue was cut into 0.3-mm slices. These slices were placed in six 35-mm dishes on 2-ml organ culture medium. Dishes received the following treatments: dish 1: ethanol; dish 2: T-3; dish 3: T-3+TAM; dish 4: TAM; dish 5: E-2; dish 6: E-2+TAM. TGF-alpha mRNA content was normalized to glyceraldehyde-3-phosphate dehydrogenase mRNA levels. All tissues included in this study were positive for estrogen receptor (ER) and thyroid hormone receptor expression. Treatment with T-3 for 48 h significantly increased TGF-alpha mRNA levels compared to controls (15-fold), and concomitant treatment with TAM reduced expression to 3.4-fold compared to controls. When only TAM was added to the culture medium, TGF-alpha mRNA expression increased 5.3-fold, significantly higher than with all other treatment modalities. Conclusion: We demonstrate that TGF-alpha mRNA expression is more efficiently upregulated by T-3 than E-2. Concomitant treatment with TAM had a mitigating effect on the T-3 effect, while E-2 induced TGF-alpha upregulation. Our findings show some similarities between primary culture and breast cancer cell lines, but also some important differences: a) induction of TGF-alpha, a mitogenic protein, by TAM; b) a differential effect of TAM that may depend on relative expression of ER alpha and beta; and c) supraphysiological doses of T3 may induce mitogenic signals in breast cancer tissue under conditions of low circulating E-2.. Endocrinol. Invest. 31: 1047-1051, 2008) (c) 2008, Editrice Kurtis

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