Martínez-Esquivias Fernando, Gutiérrez-Angulo Melva, Pérez-Larios Alejandro, Sánchez-Burgos Jorge Alberto, Becerra-Ruiz Julieta Sarai, Guzmán-Flores Juan Manuel
Instituto de Investigación en Biociencias, Centro Universitario de Los Altos, Universidad de Guadalajara, Tepatitlán de Morelos, Jalisco, México.
Departamento de Ciencias de la Salud, Centro Universitario de los Altos, Universidad de Guadalajara, Tepatitlán de Morelos, Jalisco, México.
Anticancer Agents Med Chem. 2022;22(9):1658-1673. doi: 10.2174/1871520621666210910084216.
Health systems worldwide consider cancer a disease that causes the highest number of deaths per year. The low efficacy of current cancer therapies has led other areas of science to search for new alternatives, including nanomaterial sciences. Selenium nanoparticles have anticancer activity, as revealed by in vitro tests performed on prostate, breast, cervical, lung, colorectal, and liver cancer cell lines. Studies attribute anticancer activity to the anti-metastatic effect due to the inhibition of migration and invasion processes. The antiproliferative effect is the low expression of molecules such as cyclin D1, cyclin E, and CDK2. In addition to the activation of cell apoptosis by caspase-dependent mechanisms, there is a low expression of anti-apoptotic proteins such as Bcl-2 and a high expression of the apoptotic proteins like Bax and Bad. Other studies attribute anticancer activity to the activation of cell necroptosis, where molecules such as TNF and IRF1 participate. The pharmacological potential of selenium nanoparticles depends primarily on the administered dose, particle size, and chemical composition. Furthermore, several studies have shown that the administration of these nanoparticles is safe due to their low toxicity in non-cancerous cells. In this review, the most relevant antecedents on the anticancer potential of selenium nanoparticles in prostate, breast, cervical, lung, liver, and colorectal cancer cell lines are discussed.
全球卫生系统都认为癌症是每年导致死亡人数最多的疾病。当前癌症治疗方法的低效促使其他科学领域寻找新的替代方法,包括纳米材料科学。硒纳米颗粒具有抗癌活性,这在对前列腺癌、乳腺癌、宫颈癌、肺癌、结直肠癌和肝癌细胞系进行的体外试验中得到了证实。研究将抗癌活性归因于抑制迁移和侵袭过程所产生的抗转移作用。抗增殖作用表现为细胞周期蛋白D1、细胞周期蛋白E和细胞周期蛋白依赖性激酶2等分子的低表达。除了通过半胱天冬酶依赖性机制激活细胞凋亡外,抗凋亡蛋白如Bcl-2的表达较低,而凋亡蛋白如Bax和Bad的表达较高。其他研究将抗癌活性归因于细胞坏死性凋亡的激活,其中肿瘤坏死因子和干扰素调节因子1等分子参与其中。硒纳米颗粒的药理潜力主要取决于给药剂量、粒径和化学成分。此外,多项研究表明,由于这些纳米颗粒对非癌细胞毒性低,因此给药是安全的。在这篇综述中,我们讨论了硒纳米颗粒在前列腺癌、乳腺癌、宫颈癌、肺癌、肝癌和结直肠癌细胞系中抗癌潜力的最相关研究进展。