Istituto di Genetica Molecolare CNR, 27100 Pavia, Italy ; Departamento de Ciencias de la Salud, Universidad Técnica Particular de Loja, San Cayetano Alto, Calle París, 1101608 Loja, Ecuador.
Istituto di Genetica Molecolare CNR, 27100 Pavia, Italy.
Biomed Res Int. 2014;2014:924585. doi: 10.1155/2014/924585. Epub 2014 Jun 18.
The pharmacological use of the plant alkaloid berberine is based on its antibacterial and anti-inflammatory properties; recently, anticancer activity has been attributed to this compound. To exploit this interesting feature, we synthesized three berberine derivatives, namely, NAX012, NAX014, and NAX018, and we tested their effects on two human colon carcinoma cell lines, that is, HCT116 and SW613-B3, which are characterized by wt and mutated p53, respectively. We observed that cell proliferation is more affected by cell treatment with the derivatives than with the lead compound; moreover, the derivatives proved to induce cell cycle arrest and cell death through apoptosis, thus suggesting that they could be promising anticancer drugs. Finally, we detected typical signs of autophagy in cells treated with berberine derivatives.
植物生物碱小檗碱的药理学用途基于其抗菌和抗炎特性;最近,该化合物被认为具有抗癌活性。为了利用这一有趣的特性,我们合成了三种小檗碱衍生物,即 NAX012、NAX014 和 NAX018,并测试了它们对两种人结肠癌细胞系 HCT116 和 SW613-B3 的影响,这两种细胞系分别具有 wt 和突变型 p53。我们观察到细胞增殖受衍生物处理的影响比受先导化合物处理的影响更大;此外,衍生物通过细胞凋亡诱导细胞周期停滞和细胞死亡,因此表明它们可能是有前途的抗癌药物。最后,我们在用小檗碱衍生物处理的细胞中检测到典型的自噬迹象。