Faculty of Biology and Biotechnologies, Higher School of Economics, Moscow, 101000, Russia; P. A. Hertsen Moscow Oncology Research Center, Branch of the National Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, 125284, Russia.
P. A. Hertsen Moscow Oncology Research Center, Branch of the National Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, 125284, Russia.
Biochimie. 2020 Dec;179:217-227. doi: 10.1016/j.biochi.2020.10.007. Epub 2020 Oct 22.
Epigenetic alterations represent promising therapeutic targets in cancer treatment. Recently it was revealed that small molecules have the potential to act as microRNA silencers. Capacity to bind the discrete stem-looped structure of pre-miR-21 and prevent its maturation opens opportunities to utilize such compounds for the prevention of initiation, progression, and chemoresistance of cancer. Molecular simulations performed earlier identified 3,3'-diindolylmethane (DIM) as a potent microRNA-21 antagonist. However, data on DIM and microRNA-21 interplay is controversial, which may be caused by the limitations of the cell lines.
表观遗传改变是癌症治疗中很有前途的治疗靶点。最近发现,小分子具有作为 microRNA 沉默子的潜力。能够结合 pre-miR-21 的离散茎环结构并阻止其成熟,为利用这些化合物预防癌症的起始、进展和化疗耐药性提供了机会。早期进行的分子模拟鉴定出 3,3'-二吲哚甲烷 (DIM) 是一种有效的 microRNA-21 拮抗剂。然而,关于 DIM 和 microRNA-21 相互作用的数据存在争议,这可能是由于细胞系的局限性造成的。