Publication: Tamoxifen inhibits transforming growth factor-alpha gene expression in human breast carcinoma samples treated with triiodothyronine
dc.contributor.author | Condel, S. J. | |
dc.contributor.author | Luvizotto, R. A. M. | |
dc.contributor.author | Sibio, M. T. | |
dc.contributor.author | Katayama, M. L. H. | |
dc.contributor.author | Brentani, M. M. | |
dc.contributor.author | Nogueira, Célia Regina [UNESP] | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2014-05-20T13:33:18Z | |
dc.date.available | 2014-05-20T13:33:18Z | |
dc.date.issued | 2008-12-01 | |
dc.description.abstract | 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 | en |
dc.description.affiliation | UNESP, Fac Med, Dept Clin Med, Div Endocrinol & Metab, BR-18618970 Botucatu, SP, Brazil | |
dc.description.affiliation | Univ São Paulo, Dept Radiol, Div Oncol, BR-09500900 São Paulo, Brazil | |
dc.description.affiliationUnesp | UNESP, Fac Med, Dept Clin Med, Div Endocrinol & Metab, BR-18618970 Botucatu, SP, Brazil | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.sponsorshipId | FAPESP: 04/12338-7 | |
dc.description.sponsorshipId | FAPESP: 05/55459-1 | |
dc.format.extent | 1047-1051 | |
dc.identifier | http://www.ncbi.nlm.nih.gov/pubmed/19246968 | |
dc.identifier.citation | Journal of Endocrinological Investigation. Milan: Editrice Kurtis S R L, v. 31, n. 12, p. 1047-1051, 2008. | |
dc.identifier.issn | 0391-4097 | |
dc.identifier.uri | http://hdl.handle.net/11449/11391 | |
dc.identifier.wos | WOS:000264081900003 | |
dc.language.iso | eng | |
dc.publisher | Editrice Kurtis S R L | |
dc.relation.ispartof | Journal of Endocrinological Investigation | |
dc.relation.ispartofsjr | 1,076 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | Breast cancer samples | en |
dc.subject | estrogen | en |
dc.subject | tamoxifen | en |
dc.subject | TGF-alpha | en |
dc.subject | triiodothyronine | en |
dc.title | Tamoxifen inhibits transforming growth factor-alpha gene expression in human breast carcinoma samples treated with triiodothyronine | en |
dc.type | Artigo | |
dcterms.rightsHolder | Editrice Kurtis S R L | |
dspace.entity.type | Publication | |
unesp.author.lattes | 7607038776901890[6] | |
unesp.author.orcid | 0000-0002-7354-9518[6] | |
unesp.author.orcid | 0000-0002-4014-0660[6] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatu | pt |
unesp.department | Clínica Médica - FMB | pt |
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