Biomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.
Department of Chemistry and Biochemistry, Florida International University, Miami, Florida 33199, United States.
Chem Res Toxicol. 2023 Apr 17;36(4):660-668. doi: 10.1021/acs.chemrestox.2c00367. Epub 2023 Mar 31.
Here, we reported a spontaneous reaction between anticancer drug doxorubicin and GTP or dGTP. Incubation of doxorubicin with GTP or dGTP at 37 °C or above yields a covalent product: the doxorubicin-GTP or -dGTP conjugate where a covalent bond is formed between the C14 position of doxorubicin and the 2-amino group of guanine. Density functional theory calculations show the feasibility of this spontaneous reaction. Fluorescence imaging studies demonstrate that the doxorubicin-GTP and -dGTP conjugates cannot enter nuclei although they rapidly accumulate in human SK-OV-3 and NCI/ADR-RES cells. Consequently, the doxorubicin-GTP and -dGTP conjugates are less cytotoxic than doxorubicin. We also demonstrate that doxorubicin binds to ATP, GTP, and other nucleotides with a dissociation constant () in the sub-millimolar range. Since human cells contain millimolar levels of ATP and GTP, these results suggest that doxorubicin may target ATP and GTP, energy molecules that support essential processes in living organisms.
在这里,我们报道了抗癌药物阿霉素与 GTP 或 dGTP 之间的自发反应。在 37°C 或更高温度下,阿霉素与 GTP 或 dGTP 孵育会产生一个共价产物:阿霉素-GTP 或 -dGTP 缀合物,其中阿霉素的 C14 位与鸟嘌呤的 2-氨基之间形成了共价键。密度泛函理论计算表明了这种自发反应的可行性。荧光成像研究表明,尽管阿霉素-GTP 和 -dGTP 缀合物迅速积累在人 SK-OV-3 和 NCI/ADR-RES 细胞中,但它们不能进入细胞核。因此,阿霉素-GTP 和 -dGTP 缀合物的细胞毒性比阿霉素低。我们还证明,阿霉素与 ATP、GTP 和其他核苷酸的结合解离常数()在亚毫摩尔范围内。由于人类细胞中含有毫摩尔级别的 ATP 和 GTP,这些结果表明阿霉素可能靶向支持生物体内基本过程的能量分子 ATP 和 GTP。