Hence, these two fractions could be considered as potential chemotherapeutics in malignancy therapy. In order to detect the type of cell death BRL-50481 operating in cells treated with chloroform and ethyl acetate treatments as the most effective extracts, different cell death mechanisms were investigated. are magnificently nutritious and are generally used as a part of the diet in Iran. They have health enhancing benefits including anticancer properties due to the presence of numerous bioactive compounds. Herein, we investigated in vitro and in vivo anticancer properties of components. Methods Anti-growth activity of different fractions was explored in vitro on different cancerous cells using MTT assay, Annexin V/PI and SA–gal staining, Western blotting, flowcytometric and immunofluorescence microscopic evaluations. In vivo antitumor BRL-50481 activity was investigated in BALB/c mice bearing 4?T1 mammary carcinoma cells. Results We shown that chloroformic and ethyl acetate fractions exert cytotoxic activity toward MDA-MB-231 cells, probably the most sensitive cell collection, after 72?h of treatment with IC50 ideals of 0.005 and 0.006?mg/ml, respectively. Incubation of MDA-MB-231 cells with ? and ? IC50-72h concentrations of each portion resulted in a significant G2/M cell cycle arrest. ? IC50-72h concentration of the chloroform portion led to the disruption of polymerization in mitotic microtubules. Exposure of human breast malignancy cells to different concentrations of the components at different incubation occasions did not induce apoptosis, autophagy or senescence. Our in vivo study exposed that administration of the chloroform draw out at a dose of 1 1?mg/kg/day time strongly suppressed mammary tumor progression and decreased the number of proliferative cells in the lung cells indicating its anti-metastatic effect. Conclusion Our findings imply that the chloroform portion of possesses the suppressive action on breast malignancy through mitotic cell cycle arrest suggesting a mechanism associated with disturbing microtubule polymerization. Electronic supplementary material The online version of this article (10.1186/s12906-019-2522-8) contains supplementary material, which is available to authorized users. is definitely native to Iran and grows within the Zagros mountains. Besides its software in traditional medicine, this flower is used to get ready a broad range of local foods. To day, has been found to have pharmacological properties including analgesic effect , inhibition of platelet aggregation  and renal stone formation  as well as anticancer activity . To the best of our knowledge, there is no investigation of the anticancer activity of components. This motivated us to explore the in vitro and in vivo anticancer activity of different components from aerial parts. Methods Flower material and preparation of components was collected from Shiraz, Iran, in the spring, authenticated by Dr.Shahin Zarre and deposited in the Herbarium of Faculty of Sciences, Tehran University or college, Tehran, Iran (Voucher No:45496). The aerial parts were air flow dried prior to becoming grinded into powder. 50?g of dried powder was mixed with ethanol: water (80:20) at space temperature in order to obtain total draw out. In addition, 100?g BRL-50481 of flower powder was extracted sequentially by solvents with a Rabbit Polyclonal to PTPRZ1 BRL-50481 wide range of polarities including n-hexane, chloroform, ethyl acetate and methanol using a maceration process. The process was repeated 3 times with the same flower material but using new solvents [36C38]. The components were then filtered and evaporated to dryness on a rotary evaporator under reduced pressure below 40?C. All the components were stored at 4?C until utilized for experiments. The yield of extraction for total extract, n-hexane, chloroform, ethyl acetate and methanol fractions were as follows: 32.57, 1.63, 1.08, 0.4 and 15.25%, respectively. Chemicals and cell lines MDA-MB-231 (human being breast adenocarcinoma, C578), MCF-7 (human being breast adenocarcinoma, C135), HT-29 (human being colorectal adenocarcinoma, C466), HepG2 (liver hepatocellular carcinoma, C158), 4?T1(mouse mammary tumor, C604) and NIH3T3 (mouse embryonic fibroblasts, C156) cell lines were purchased from your cell lender of Pasture Institute of Iran (NCBI). Cells were cultured in Dulbeccos Modified Eagles Medium (DMEM) medium comprising 10% fetal bovine serum (FBS), 100?U/ml penicillin and 100?g/ml streptomycin (GibcoBRL, Rockville, IN, USA) at 37?C with 5% CO2 inside a humidified atmosphere inside a CO2 incubator..