Background: Breast cancer is a malignant proliferation of epithelial cells that lining theducts or lobules of the breast. Breast cancer is the second common cancer (after lungcancer) in women. Gallic acid, being a polyphenols, has been reported for its antiproliferativeactivity against many cancer cell lines. Objective of the present study is effect ofgallic acid on proliferation and apoptosis of the human breast adenocarcinoma cell linesSKBR3 and normal fibroblasts cells. Methods: This experimental study was performed in cellular and developmental biologyof Shahrekord Islamic Azad University, Iran from April to August 2015. For anticanceractivity, in this study SKBR3 cells and normal fibroblast cells (HU-02) werecultured in Dulbecco's modified eagle's medium, DMEM (Gibco, Life Technologies, Inc., New York, USA) medium with 10% fetal bovine serum, FBS (Gibco, Life Technologies, Inc., New York, USA). The SKBR3 and normal fibroblast cells were treatedin the medium of DMEM medium and gallic acid (20, 40, 80, 100 and 200 μ g/ml) for24, 48 and 72 hours. Cells viability was assessed by MTS (Methyl-Thiazol-) assay. Cells were seeded at 5×103 cells/ml in 96 well plates and incubated for 24 hours. Thenmetabolites of bacteria were added, after indicated times MTS (20μ l) was added andthe absorbance was measured at 492 nm using ELISA plate reader. The percentage ofapoptosis induction was determined by flow cytometry analysis using Annexin-V fluoresceinisothiocyanate (FITC) kit (BioVision Products, CA, USA) in 20, 40, 80, 100and 200 μ g/ml concentration of gallic acid at 48 hours incubation. Results: Gallic acid decreases significantly the viability of SKBR3 cell line in a timeand dose dependent manner. So that the most effective concentration of this substancewas 200 μ g/ml and 72 hours after treatment (P< 0. 05). According to the data of Annexin-PI, the highest apoptosis induction rate was seen in 200 μ g/ml (P< 0. 05). While gallicacid in various concentrations had no significant effect on normal fibroblast cells. Conclusion: Objective of the present study is effect of gallic acid on proliferation and apoptosisof the human breast adenocarcinoma cell lines SKBR3 and normal fibroblasts cells.