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一种有效的体外和体内抗肿瘤活性的强氨基萘酰亚胺铂(IV)配合物,对肿瘤细胞显示双重 DNA 损伤作用。

A potent aminonaphthalimide platinum(IV) complex with effective antitumor activities in vitro and in vivo displaying dual DNA damage effects on tumor cells.

机构信息

Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng 252059, PR China.

Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng 252059, PR China.

出版信息

Bioorg Med Chem Lett. 2019 Oct 15;29(20):126670. doi: 10.1016/j.bmcl.2019.126670. Epub 2019 Sep 4.

Abstract

A new aminonaphthalimide platinum(IV) complex was developed by incorporating aminonaphthalimide, a DNA intercalator, into the platinum(IV) system. This complex displayed potent antitumor activities against all tested tumor cell lines in vitro and showed great potential in overcoming drug resistance of cisplatin. Moreover, it remarkably inhibited the growth of CT26 xenografts in BALB/c mice without severe side effects in vivo. Then, the compound exhibited a dual DNA damage antitumor mechanism that it could interact with DNA in tetravalent form via the naphthalimide group to cause DNA lesion, and the further liberation of platinum(II) complex after reduction would induce remarkable secondary damage to DNA. Meanwhile, it caused cell apoptosis through an intrinsic apoptosis pathway by up-regulating the expression of caspase 3 and caspase 9.

摘要

一种新型的含氨基萘酰亚胺的铂(IV)配合物被开发出来,它将氨基萘酰亚胺(一种 DNA 嵌入剂)整合到铂(IV)系统中。该配合物在体外对所有测试的肿瘤细胞系均显示出强大的抗肿瘤活性,并显示出克服顺铂耐药性的巨大潜力。此外,它在体内显著抑制了 BALB/c 小鼠 CT26 异种移植瘤的生长,没有严重的副作用。然后,该化合物表现出一种双重的 DNA 损伤抗肿瘤机制,它可以通过萘酰亚胺基团与四价形式的 DNA 相互作用,导致 DNA 损伤,而进一步还原后释放的铂(II)配合物会对 DNA 造成显著的二次损伤。同时,它通过上调半胱氨酸天冬氨酸蛋白酶 3 和半胱氨酸天冬氨酸蛋白酶 9 的表达,通过内在凋亡途径引起细胞凋亡。

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