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Alterações epigenéticas e do número de cópias do gene SFN em carcinomas mamários

2014; Linguagem: Inglês

2639-6459

Danielle Barbosa Brotto,

Histone Deacetylase Inhibitors Research

The SFN gene (Stratifin; 14-3-3 sigma) plays roles as a tumor suppressor gene and its expression is induced in response to DNA damage by disabling the cell cycle arrest at the G2/M checkpoint. Inactivation or down-regulation of gene expression levels has been generally attributed to the hypermethylation of its CpG island, identified as a common mechanism in a variety of human cancers, also associated to treatment response. The aim of the present study was to characterize epigenetics and genetics alterations of the SFN gene in primary breast cancer and to investigate the relationship with clinical and histopatological variables. In addition, cell lines derived from normal breast and breast cancer tissues, were employed to identify the effect of copy number dosage and DNA methylation pattern in gene expression, besides the study of combined response to 5-Aza-dC (5-Aza-2’-Deoxycytidine) and radiation exposure on cell survival. After sodium bisulfite modification, the DNA methylation pattern was determined by Methylation-Specific Polymerase Chain Reaction (MS-PCR) in a series of 84 Breast cancer samples (76 infiltrating ductal carcinomas, 5 infiltrating lobular, 1 metaplasic, 1 apocrine and 1 papillary) as well as in a panel of 20 human cell lines (3 derived from normal breast and 17 from breast cancer). SFN copy number was performed using relative quantification, by qPCR (quantitative Polimerase Chain Reaction) in 82 samples. Transcript levels were evaluated by RT-qPCR within a selection of 8 cell lines, based on DNA methylation, SFN copy number dosage and p53 status. Ionizing radiation effect was studied through MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay, by using a single dose of 4 Gy at different time intervals (12, 24, 48 and 72h) in tree cell lines (T47D, MDA-MB-231 e MDA-MB-436) treated or not with 5-Aza-dC. SFN methylation was observed in 79% of primary breast cancer, while copy number alterations occurred at lower frequencies. Univariate analysis showed that clinical stage (p=0.0045), lymph nodes involvement (p= 0.0189) and metastasis occurrence (p= 0.0003) were independent parameters related to desease-specific survival rate. Amongst 76 infiltrating ductal carcinomas, absence of SFN methylation was associated with a decreased overall survival (Log-rank test, p=0.0036) and metastasis occurrence (Fisher’s exact test, p= 0, 021). As expected, breast cell lines showed gene expression levels reliant to methylation pattern and gene copy number. 5-Aza-dC treatment lead to reactivation of SFN gene expression in methylated cell lines (BT-483 e MDA-MB-436), with a mild reactivation in Hs578T cell line. The combination of 5-Aza-dC and radiation exposure showed greater effect in MDA-MB-231 and MDA-MB-436 (basal subtype), though the opposite was seen in T47D cell line (luminal subtype). These findings endorse that abnormal SFN methylation occurs in high frequencies in breast cancers, nevertheless, patients with unmethylated tumors exhibit a worst prognosis. Primary methylation status of the cell lines might be related to differences in responses after 5-Aza-dC followed by radiation exposure. However, further studies are necessary to investigate the potential role of the SFN gene as useful prognostic and predictive marker. Key-words: breast cancer, SFN gene, DNA methylation, copy number alterations, prognostic marker.