Kocik Justyna, Machula Monika, Wisniewska Aneta, Surmiak Ewa, Holak Tad A, Skalniak Lukasz
Department of Organic Chemistry, Faculty of Chemistry, Jagiellonian University, ul. Gronostajowa 2, 30-387 Krakow, Poland.
Cancers (Basel). 2019 Jul 19;11(7):1014. doi: 10.3390/cancers11071014.
The protein p53, known as the "Guardian of the Genome", plays an important role in maintaining DNA integrity, providing protection against cancer-promoting mutations. Dysfunction of p53 is observed in almost every cancer, with 50% of cases bearing loss-of-function mutations/deletions in the gene. In the remaining 50% of cases the overexpression of HDM2 (mouse double minute 2, human homolog) protein, which is a natural inhibitor of p53, is the most common way of keeping p53 inactive. Disruption of HDM2-p53 interaction with the use of HDM2 antagonists leads to the release of p53 and expression of its target genes, engaged in the induction of cell cycle arrest, DNA repair, senescence, and apoptosis. The induction of apoptosis, however, is restricted to only a handful of p53 cells, and, generally, cancer cells treated with HDM2 antagonists are not efficiently eliminated. For this reason, HDM2 antagonists were tested in combinations with multiple other therapeutics in a search for synergy that would enhance the cancer eradication. This manuscript aims at reviewing the recent progress in developing strategies of combined cancer treatment with the use of HDM2 antagonists.
蛋白质p53被誉为“基因组守护者”,在维持DNA完整性、预防促癌突变方面发挥着重要作用。几乎在每种癌症中都能观察到p53功能失调,其中50%的病例该基因存在功能丧失性突变/缺失。在其余50%的病例中,p53的天然抑制剂HDM2(小鼠双微体2,人类同源物)蛋白的过表达是使p53保持失活的最常见方式。使用HDM2拮抗剂破坏HDM2与p53的相互作用会导致p53释放及其靶基因表达,这些靶基因参与诱导细胞周期停滞、DNA修复、衰老和凋亡。然而,凋亡诱导仅局限于少数p53细胞,一般而言,用HDM2拮抗剂处理的癌细胞并不能被有效清除。因此,人们对HDM2拮抗剂与多种其他疗法联合进行了测试,以寻找能增强癌症根除效果的协同作用。本手稿旨在综述使用HDM2拮抗剂联合癌症治疗策略的最新进展。