Department of Pharmacy and Biotechnology, Alma Mater Studiorum University of Bologna, via Selmi 3, 40126, Bologna, Italy.
Mol Cancer. 2022 Sep 17;21(1):180. doi: 10.1186/s12943-022-01649-y.
G-quadruplex (G4) binders have been investigated to discover new anticancer drugs worldwide in past decades. As these ligands are generally not highly cytotoxic, the discovery rational was mainly based on increasing the cell-killing potency. Nevertheless, no G4 binder has been shown yet to be effective in cancer patients. Here, G4 binder activity at low dosages will be discussed as a critical feature to discover ligands with therapeutic effects in cancer patients. Specific effects of G4 binders al low doses have been reported to occur in cancer and normal cells. Among them, genome instability and the stimulation of cytoplasmic processes related to autophagy and innate immune response open to the use of G4 binders as immune-stimulating agents. Thus, we propose a new rational of drug discovery, which is not based on cytotoxic potency but rather on immune gene activation at non-cytotoxic dosage.
在过去的几十年中,全世界一直在研究 G-四链体 (G4) 结合物,以发现新的抗癌药物。由于这些配体通常没有高度的细胞毒性,因此发现的合理依据主要是提高细胞杀伤能力。然而,目前还没有发现任何 G4 结合物在癌症患者中有效。在这里,我们将讨论低剂量 G4 结合物的活性,作为在癌症患者中发现具有治疗效果的配体的关键特征。已经报道了低剂量 G4 结合物在癌细胞和正常细胞中会产生特定的作用。其中,基因组不稳定性和与自噬和先天免疫反应相关的细胞质过程的刺激为 G4 结合物作为免疫刺激剂的应用开辟了道路。因此,我们提出了一种新的药物发现理念,它不是基于细胞毒性,而是基于非细胞毒性剂量下免疫基因的激活。