Sztiller-Sikorska Malgorzata, Czyz Malgorzata
Department of Molecular Biology of Cancer, Medical University of Lodz, 6/8 Mazowiecka Street, 92-215 Lodz, Poland.
Pharmaceuticals (Basel). 2020 Aug 14;13(8):194. doi: 10.3390/ph13080194.
Primary and acquired resistance of cancer to therapy is often associated with activation of nuclear factor kappa B (NF-κB). Parthenolide (PN) has been shown to inhibit NF-κB signaling and other pro-survival signaling pathways, induce apoptosis and reduce a subpopulation of cancer stem-like cells in several cancers. Multimodal therapies that include PN or its derivatives seem to be promising approaches enhancing sensitivity of cancer cells to therapy and diminishing development of resistance. A number of studies have demonstrated that several drugs with various targets and mechanisms of action can cooperate with PN to eliminate cancer cells or inhibit their proliferation. This review summarizes the current state of knowledge on PN activity and its potential utility as complementary therapy against different cancers.
癌症对治疗的原发性和获得性耐药通常与核因子κB(NF-κB)的激活有关。小白菊内酯(PN)已被证明可抑制NF-κB信号传导和其他促生存信号通路,诱导凋亡并减少几种癌症中癌干细胞样亚群。包括PN或其衍生物的多模式疗法似乎是增强癌细胞对治疗的敏感性并减少耐药性发展的有前景的方法。多项研究表明,几种具有不同靶点和作用机制的药物可与PN协同作用以消除癌细胞或抑制其增殖。本综述总结了关于PN活性及其作为针对不同癌症的辅助治疗的潜在效用的当前知识状态。