Zalutskii I V, Lukianova N Y, Storchai D M, Burlaka A P, Shvets Y V, Borikun T V, Todor I M, Lukashevich V S, Rudnichenko Y A, Chekhun V F
State Scientific Institution "Institute of Physiology", NAS of Belarus, Minsk 220072, Republic of Belarus.
R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, NAS of Ukraine, Kyiv 03022, Ukraine.
Exp Oncol. 2017 Jul;39(2):106-111.
To investigate the mechanisms of cytotoxic activity and pro-/antioxidant effect of lactoferrin on hormone receptor-positive and receptor-negative breast cancer cells in vitro.
The study was performed on receptor-positive (MCF-7, T47D) and receptor-negative (MDA-MB-231, MDA-MB-468) human breast cancer cell lines. Immunocytochemical staining, flow cytometry, low-temperature electron paramagnetic resonance, and the Comet assay were used.
Upon treatment with lactoferrin, the increased levels of reactive oxygen species (ROS) (p < 0.05), NO generation rate by inducible NO-synthase (p < 0.05) and the level of "free" iron (p < 0.05) were observed. Moreover, the effects of lactoferrin were more pronounced in receptor-negative MDA-MB-231 and MDA-MB-468 cells. These changes resulted in increased expression of proapoptotic Bax protein (p < 0.05), reduced expression of the antiapoptotic Bcl-2 protein (p < 0.05) and level of not-oxidized mitochondrial cardiolipin (1.4-1.7-fold, p < 0.05). This, in turn, caused an increase in the percentage of apoptotic cells (by 14-24%, p < 0.05). Cytotoxic effects of lactoferrin were accompanied by an increase in the percentage of DNA in the comet tail and blocking cell cycle at G2/M phase, especially in receptor-negative cell lines.
The study showed that exogenous lactoferrin causes a violation of an antioxidant balance by increasing the level of ROS, "free" iron and NO generation rate, resalting in the blocking of cell cycle at G2/M-phase and apoptosis of malignant cells.
研究乳铁蛋白在体外对激素受体阳性和受体阴性乳腺癌细胞的细胞毒活性机制以及促/抗氧化作用。
本研究采用受体阳性(MCF-7、T47D)和受体阴性(MDA-MB-231、MDA-MB-468)人乳腺癌细胞系。使用了免疫细胞化学染色、流式细胞术、低温电子顺磁共振和彗星试验。
用乳铁蛋白处理后,观察到活性氧(ROS)水平升高(p < 0.05)、诱导型一氧化氮合酶产生一氧化氮的速率升高(p < 0.05)以及“游离”铁水平升高(p < 0.05)。此外,乳铁蛋白对受体阴性的MDA-MB-231和MDA-MB-468细胞的作用更明显。这些变化导致促凋亡的Bax蛋白表达增加(p < 0.05)、抗凋亡的Bcl-2蛋白表达降低(p < 0.05)以及未氧化的线粒体心磷脂水平降低(1.4 - 1.7倍,p < 0.05)。这进而导致凋亡细胞百分比增加(14% - 24%,p < 0.05)。乳铁蛋白的细胞毒作用伴随着彗星尾中DNA百分比的增加以及细胞周期在G2/M期的阻滞,尤其是在受体阴性细胞系中。
该研究表明,外源性乳铁蛋白通过提高ROS水平、“游离”铁水平和一氧化氮产生速率,导致抗氧化平衡失调,从而使细胞周期在G2/M期阻滞并使恶性细胞凋亡。