Milković Lidija, Mlinarić Monika, Lučić Ivan, Čipak Gašparović Ana
Division of Molecular Medicine, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Cancers (Basel). 2023 Dec 8;15(24):5747. doi: 10.3390/cancers15245747.
Breast cancer is still the leading cause of death in women of all ages. The reason for this is therapy resistance, which leads to the progression of the disease and the formation of metastases. Multidrug resistance (MDR) is a multifactorial process that leads to therapy failure. MDR involves multiple processes and many signaling pathways that support each other, making it difficult to overcome once established. Here, we discuss cellular-oxidative-stress-modulating factors focusing on transcription factors NRF2, FOXO family, and peroxiporins, as well as their possible contribution to MDR. This is significant because oxidative stress is a consequence of radiotherapy, chemotherapy, and immunotherapy, and the activation of detoxification pathways could modulate the cellular response to therapy and could support MDR. These proteins are not directly responsible for MDR, but they support the survival of cancer cells under stress conditions.
乳腺癌仍是各年龄段女性的主要死因。其原因在于治疗耐药性,这会导致疾病进展和转移的形成。多药耐药(MDR)是一个多因素过程,会导致治疗失败。MDR涉及多个相互支持的过程和许多信号通路,一旦形成就难以克服。在此,我们讨论细胞氧化应激调节因子,重点关注转录因子NRF2、FOXO家族和过氧化物酶体蛋白,以及它们对MDR的可能作用。这一点很重要,因为氧化应激是放疗、化疗和免疫治疗的结果,解毒途径的激活可以调节细胞对治疗的反应,并可能支持MDR。这些蛋白质并非直接导致MDR,但它们能在应激条件下支持癌细胞的存活。