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尿嘧啶DNA糖基化酶在正常人细胞中切除5-氟尿嘧啶的机制。

Mechanisms of excision of 5-fluorouracil by uracil DNA glycosylase in normal human cells.

作者信息

Mauro D J, De Riel J K, Tallarida R J, Sirover M A

机构信息

Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

Mol Pharmacol. 1993 Jun;43(6):854-7.

PMID:8316218
Abstract

Recent evidence indicates that 5-fluorouracil (5-FlUra) is incorporated into DNA and is removed by the DNA repair enzyme uracil DNA glycosylase. Synthetic oligonucleotides containing either a single uracil or 5-FlUra residue were constructed to examine the mechanisms by which human cells remove 5-FlUra from DNA. The human uracil DNA glycosylase excised uracil in a manner similar to that observed for the bacterial enzyme. In contrast, a significant difference was observed in their abilities to remove 5-FlUra. In particular, both the bacterial and normal human enzymes displayed 13-17-fold increases in their apparent Km values but the apparent Vmax values remained virtually constant. These results demonstrate that normal human cells possess a defined capacity to remove 5-FlUra incorporated into DNA. However, specific kinetic differences may exist that affect their capacity to remove 5-FlUra formed in DNA after treatment with this cancer chemotherapeutic agent.

摘要

最近的证据表明,5-氟尿嘧啶(5-FlUra)会掺入DNA中,并被DNA修复酶尿嘧啶DNA糖基化酶清除。构建了含有单个尿嘧啶或5-FlUra残基的合成寡核苷酸,以研究人类细胞从DNA中清除5-FlUra的机制。人尿嘧啶DNA糖基化酶切除尿嘧啶的方式与细菌酶类似。相比之下,观察到它们在清除5-FlUra的能力上存在显著差异。特别是,细菌酶和正常人酶的表观Km值均增加了13-17倍,但表观Vmax值实际上保持不变。这些结果表明,正常人类细胞具有清除掺入DNA中的5-FlUra的特定能力。然而,可能存在特定的动力学差异,影响它们清除用这种癌症化疗药物处理后在DNA中形成的5-FlUra的能力。

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