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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Transcriptional effects of 1,25 dihydroxyvitamin D-3 physiological and supra-physiological concentrations in breast cancer organotypic culture

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Autor(es):
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Milani, Cintia [1] ; Hirata Katayama, Maria Lucia [1] ; de Lyra, Eduardo Carneiro [1, 2] ; Welsh, JoEllen [3] ; Campos, Laura Tojeiro [1] ; Mitzi Brentani, M. [1] ; Maciel, Maria do Socorro [4] ; Roela, Rosimeire Aparecida [1] ; del Valle, Paulo Roberto [1] ; Guedes Sampaio Goes, Joao Carlos [2] ; Nonogaki, Suely [5] ; Tamura, Rodrigo Esaki [6] ; Azevedo Koike Folgueira, Maria Aparecida [1]
Número total de Autores: 13
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Fac Med, Dept Radiol & Oncol, Disciplina Oncol, LIM24, BR-01246903 Sao Paulo - Brazil
[2] IBCC, Sao Paulo - Brazil
[3] SUNY Albany, Sch Publ Hlth, Dept Environm Hlth Sci, Rensselaer, NY 12144 - USA
[4] Hosp Canc AC Camargo, Sao Paulo - Brazil
[5] Adolfo Lutz Inst, Nucleo Patol Quantitat, Ctr Patol, Sao Paulo - Brazil
[6] ICESP, Viral Vectors Lab, Sao Paulo - Brazil
Número total de Afiliações: 6
Tipo de documento: Artigo Científico
Fonte: BMC CANCER; v. 13, MAR 15 2013.
Citações Web of Science: 20
Resumo

Background: Vitamin D transcriptional effects were linked to tumor growth control, however, the hormone targets were determined in cell cultures exposed to supra physiological concentrations of 1,25(OH)(2)D-3 (50-100nM). Our aim was to evaluate the transcriptional effects of 1,25(OH)(2)D-3 in a more physiological model of breast cancer, consisting of fresh tumor slices exposed to 1,25(OH)(2)D-3 at concentrations that can be attained in vivo. Methods: Tumor samples from post-menopausal breast cancer patients were sliced and cultured for 24 hours with or without 1,25(OH)(2)D-3 0.5nM or 100nM. Gene expression was analyzed by microarray (SAM paired analysis, FDR <= 0.1) or RT-qPCR (p <= 0.05, Friedman/Wilcoxon test). Expression of candidate genes was then evaluated in mammary epithelial/breast cancer lineages and cancer associated fibroblasts (CAFs), exposed or not to 1,25(OH)(2)D-3 0.5nM, using RT-qPCR, western blot or immunocytochemistry. Results: 1,25(OH)(2)D-3 0.5nM or 100nM effects were evaluated in five tumor samples by microarray and seven and 136 genes, respectively, were up-regulated. There was an enrichment of genes containing transcription factor binding sites for the vitamin D receptor (VDR) in samples exposed to 1,25(OH)(2)D-3 near physiological concentration. Genes up-modulated by both 1,25(OH)(2)D-3 concentrations were CYP24A1, DPP4, CA2, EFTUD1, TKTL1, KCNK3. Expression of candidate genes was subsequently evaluated in another 16 samples by RT-qPCR and up-regulation of CYP24A1, DPP4 and CA2 by 1,25(OH)(2)D-3 was confirmed. To evaluate whether the transcripitonal targets of 1,25(OH)(2)D-3 0.5nM were restricted to the epithelial or stromal compartments, gene expression was examined in HB4A, C5.4, SKBR3, MDA-MB231, MCF-7 lineages and CAFs, using RT-qPCR. In epithelial cells, there was a clear induction of CYP24A1, CA2, CD14 and IL1RL1. In fibroblasts, in addition to CYP24A1 induction, there was a trend towards up-regulation of CA2, IL1RL1, and DPP4. A higher protein expression of CD14 in epithelial cells and CA2 and DPP4 in CAFs exposed to 1,25(OH)(2)D-3 0.5nM was detected. (Continued on next page) (Continued from previous page) Conclusions: In breast cancer specimens a short period of 1,25(OH)(2)D-3 exposure at near physiological concentration modestly activates the hormone transcriptional pathway. Induction of CYP24A1, CA2, DPP4, IL1RL1 expression appears to reflect 1,25(OH)(2)D-3 effects in epithelial as well as stromal cells, however, induction of CD14 expression is likely restricted to the epithelial compartment. (AU)

Processo FAPESP: 09/10088-7 - Expressão gênica de fibroblastos associados a carcinomas de mama classificados em subtipos de acordo com receptores de estrógeno e progesterona e C-ERBB2
Beneficiário:Maria Mitzi Brentani
Linha de fomento: Auxílio à Pesquisa - Temático
Processo FAPESP: 07/04799-2 - Influência da Vitamina D na proliferação celular e no perfil de expressão gênica do câncer de mama de pacientes pós-menopausadas
Beneficiário:Maria Aparecida Azevedo Koike Folgueira
Linha de fomento: Auxílio à Pesquisa - Regular
Processo FAPESP: 08/51750-1 - Perfil de expressão gênica de fibroblastos associados ao câncer de mama submetidos ao tratamento com Vitamina D
Beneficiário:Laura Tojeiro Campos
Linha de fomento: Bolsas no Brasil - Mestrado