Mohsenikia Maryam, Alizadeh Ali Mohammad, Khodayari Saeed, Khodayari Hamid, Kouhpayeh Seyed Amin, Karimi Aliasghar, Zamani Mina, Azizian Saleh, Mohagheghi Mohammad Ali
Young Researchers and Elite Club, Islamic Azad University, Tehran Medical Branch, Tehran, Iran.
Eur J Pharmacol. 2013 Oct 15;718(1-3):1-9. doi: 10.1016/j.ejphar.2013.09.015. Epub 2013 Sep 17.
Alpha-solanine, a naturally steroidal glycoalkaloid, is found in leaves and fruits of plants as a defensive agent against fungi, bacteria and insects. Herein, we investigated solanine toxicity in vitro and in vivo, and assessed its protective and the therapeutic effects on a typical animal model of breast cancer. The study conducted in three series of experiments to obtain (i) solanine effects on cell viability of mammary carcinoma cells, (ii) in vivo toxicity of solanine, and (iv) the protective and therapeutic effects of solanine on animal model of breast cancer. Alpha-solanine significantly suppressed proliferation of mouse mammary carcinoma cells both in vitro and in vivo (P<0.05). Under the dosing procedure, 5 mg/kg solanine has been chosen for assessing its protective and therapeutic effects in mice breast cancer. Tumor take rate in the solanine-treated group was zero compared with a 75% rate in its respective control group (P<0.05). The average tumor size and weight were significantly lower in solanine-treated animals than its respective control ones (P<0.05). Proapoptotic Bax protein expression increased in breast tumor by solanine compared with its respective control group (P<0.05). Antiapoptotic Bcl-2 protein expression found to be lower in solanine-treated animals (P<0.05). Proliferative and angiogenic parameters greatly decreased in solanine-treated mice (P<0.05). Data provide evidence that solanine exerts a significant chemoprotective and chemotherapeutic effects on an animal model of breast cancer through apoptosis induction, cell proliferation and angiogenesis inhibition. These findings reveal a new therapeutic potential for solanine in cancer.
α-茄碱是一种天然甾体糖苷生物碱,存在于植物的叶子和果实中,作为抵御真菌、细菌和昆虫的防御剂。在此,我们研究了茄碱在体外和体内的毒性,并评估了其对典型乳腺癌动物模型的保护和治疗作用。该研究进行了三个系列的实验,以获得(i)茄碱对乳腺癌细胞活力的影响,(ii)茄碱的体内毒性,以及(iv)茄碱对乳腺癌动物模型的保护和治疗作用。α-茄碱在体外和体内均显著抑制小鼠乳腺癌细胞的增殖(P<0.05)。在给药过程中,选择5mg/kg的茄碱来评估其对小鼠乳腺癌的保护和治疗作用。与各自对照组75%的肿瘤发生率相比,茄碱治疗组的肿瘤发生率为零(P<0.05)。茄碱治疗的动物的平均肿瘤大小和重量明显低于各自的对照组(P<0.05)。与各自对照组相比,茄碱使乳腺肿瘤中促凋亡的Bax蛋白表达增加(P<0.05)。发现茄碱治疗的动物中抗凋亡的Bcl-2蛋白表达较低(P<0.05)。茄碱治疗的小鼠的增殖和血管生成参数大大降低(P<0.05)。数据提供了证据,表明茄碱通过诱导凋亡、抑制细胞增殖和血管生成,对乳腺癌动物模型发挥显著的化学保护和化学治疗作用。这些发现揭示了茄碱在癌症治疗中的新潜力。