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载体配体在L1210细胞铂耐药中的作用。

Role of carrier ligand in platinum resistance in L1210 cells.

作者信息

Gibbons G R, Page J D, Mauldin S K, Husain I, Chaney S G

机构信息

Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina, Chapel Hill 27599.

出版信息

Cancer Res. 1990 Oct 15;50(20):6497-501.

PMID:2208108
Abstract

We have examined the effect of carrier ligands on platinum accumulation, incorporation of platinum into DNA, cytotoxicity of Pt-DNA adducts, and repair of Pt-DNA adducts in three L1210 cell lines: L1210/0, which is sensitive to most types of platinum compounds; L1210/DDP, which is resistant to platinum compounds with the ethylenediamine (en) carrier ligand but sensitive to those with the diaminocyclohexane (dach) ligand; and L1210/DACH, which is resistant to dach-Pt compounds but sensitive to en-Pt compounds. There was a selective decrease in accumulation of dach-Pt in the L1210/DACH line and of en-Pt in the L1210/DDP line. Intracellular dach-Pt was incorporated into DNA to a lesser extent than en-Pt in both resistant cell lines. Cytotoxicity of en-Pt adducts was less than that of dach-Pt adducts in the L1210/DDP line, while the reverse was true in the L1210/DACH line. Increased repair was seen in both resistant cell lines; a carrier ligand effect was seen only in the L1210/DDP line, which showed a greater initial rate of repair for en-Pt than dach-Pt adducts. These data suggest that carrier ligand effects seen in resistant cell lines may be due, in part, to differences in accumulation of platinum, repair of Pt-DNA adducts, and tolerance of Pt-DNA adducts.

摘要

我们研究了载体配体对三种L1210细胞系中铂积累、铂掺入DNA、Pt-DNA加合物的细胞毒性以及Pt-DNA加合物修复的影响:L1210/0,对大多数类型的铂化合物敏感;L1210/DDP,对带有乙二胺(en)载体配体的铂化合物耐药,但对带有二氨基环己烷(dach)配体的铂化合物敏感;以及L1210/DACH,对dach-Pt化合物耐药,但对en-Pt化合物敏感。在L1210/DACH细胞系中,dach-Pt的积累有选择性地减少,在L1210/DDP细胞系中,en-Pt的积累有选择性地减少。在这两种耐药细胞系中,细胞内dach-Pt掺入DNA的程度均低于en-Pt。在L1210/DDP细胞系中,en-Pt加合物的细胞毒性小于dach-Pt加合物,而在L1210/DACH细胞系中情况则相反。在两种耐药细胞系中均观察到修复增加;仅在L1210/DDP细胞系中观察到载体配体效应,该细胞系中en-Pt加合物的初始修复速率高于dach-Pt加合物。这些数据表明,在耐药细胞系中观察到的载体配体效应可能部分归因于铂积累、Pt-DNA加合物修复以及对Pt-DNA加合物耐受性的差异。

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