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阿霉素-DNA加合物的体外形成

Formation of adriamycin--DNA adducts in vitro.

作者信息

Cullinane C, Cutts S M, van Rosmalen A, Phillips D R

机构信息

Department of Biochemistry, La Trobe University, Bundoora, Victoria, Australia.

出版信息

Nucleic Acids Res. 1994 Jun 25;22(12):2296-303. doi: 10.1093/nar/22.12.2296.

DOI:10.1093/nar/22.12.2296
PMID:8036157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC523687/
Abstract

Adriamycin is known to induce the formation of adducts with DNA when reacted under in vitro transcription conditions. The factors affecting the extent of adduct formation were examined in order to establish the critical components and optimal conditions required for the reaction, and to gain insight into the nature of the DNA-adduct complex. There was a strong dependence on reaction temperature (with a 40-fold increase of adducts at 40-50 degrees C compared to 10 degrees C), pH (maximum adducts at pH 7), but little dependence on the oxygen level. There was an absolute requirement for a reducing agent, with adducts detected with DTT, beta-mercaptoethanol and glutathione, maximal adducts were formed at high levels of DTT (5-10 mM). Adducts were also formed with a xanthine oxidase/NADH reducing system, with increasing amounts of adducts detected with increasing NADH; no adducts were detected in the absence of either the enzyme or NADH. Of fourteen derivatives studied, only four yielded a similar extent of adduct formation as adriamycin; there was no absolute requirement for a carbonyl at C13 or hydroxyl at C14. Adducts were also observed with ssDNA but required a longer reaction time compared to dsDNA. The sequence specificity of adduct formation with ssDNA was examined using a primer-extension assay; almost all adducts were associated with a guanine residue. Overall, the results are consistent with a two-step reaction mechanism involving reductive activation of adriamycin, with the activated species then reacting with the guanine residues of either dsDNA or ssDNA.

摘要

已知阿霉素在体外转录条件下反应时会诱导与DNA形成加合物。为确定反应所需的关键成分和最佳条件,并深入了解DNA - 加合物复合物的性质,研究了影响加合物形成程度的因素。加合物形成程度强烈依赖于反应温度(40 - 50摄氏度时的加合物比10摄氏度时增加40倍)、pH值(pH 7时加合物最多),但对氧气水平依赖性较小。反应绝对需要还原剂,用二硫苏糖醇(DTT)、β - 巯基乙醇和谷胱甘肽可检测到加合物,在高浓度DTT(5 - 10 mM)时形成的加合物最多。用黄嘌呤氧化酶/NADH还原系统也能形成加合物,随着NADH增加检测到的加合物量增多;在没有酶或NADH时未检测到加合物。在所研究的14种衍生物中,只有4种产生的加合物形成程度与阿霉素相似;对C13处的羰基或C14处的羟基没有绝对要求。与单链DNA(ssDNA)也能形成加合物,但与双链DNA(dsDNA)相比需要更长的反应时间。使用引物延伸试验检测了与ssDNA形成加合物的序列特异性;几乎所有加合物都与鸟嘌呤残基相关。总体而言,结果与涉及阿霉素还原活化的两步反应机制一致,活化后的物种随后与dsDNA或ssDNA的鸟嘌呤残基反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ad/523687/83c0455f475b/nar00036-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ad/523687/83c0455f475b/nar00036-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ad/523687/83c0455f475b/nar00036-0128-a.jpg

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本文引用的文献

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DITHIOTHREITOL, A NEW PROTECTIVE REAGENT FOR SH GROUPS.二硫苏糖醇,一种新的巯基保护剂。
Biochemistry. 1964 Apr;3:480-2. doi: 10.1021/bi00892a002.
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Circumvention of resistance by doxorubicin, but not by idarubicin, in a human leukemia cell line containing an intercalator-resistant form of topoisomerase II: evidence for a non-topoisomerase II-mediated mechanism of doxorubicin cytotoxicity.在一种含有拓扑异构酶II嵌入抗性形式的人白血病细胞系中,阿霉素可规避耐药性,但伊达比星不能:阿霉素细胞毒性的非拓扑异构酶II介导机制的证据。
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Solution chemistry studies of adriamycin--iron complexes present in vivo.
一种用于定量肿瘤和组织中与DNA结合的阿霉素的灵敏高效液相色谱测定法。
J Pharm Biomed Anal. 2016 Feb 5;119:122-9. doi: 10.1016/j.jpba.2015.11.035. Epub 2015 Nov 28.
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Adriamycin-Induced Models of VACTERL Association.阿霉素诱导的VACTERL综合征模型。
Mol Syndromol. 2013 Feb;4(1-2):46-62. doi: 10.1159/000345579.
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Importance of intracellular pH in determining the uptake and efficacy of the weakly basic chemotherapeutic drug, doxorubicin.细胞内 pH 值在确定弱碱性化疗药物多柔比星的摄取和疗效中的重要性。
PLoS One. 2012;7(4):e35949. doi: 10.1371/journal.pone.0035949. Epub 2012 Apr 26.
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Detection of Adriamycin-DNA adducts by accelerator mass spectrometry at clinically relevant Adriamycin concentrations.在临床相关阿霉素浓度下通过加速器质谱法检测阿霉素 - DNA加合物
Nucleic Acids Res. 2008 Sep;36(16):e100. doi: 10.1093/nar/gkn439. Epub 2008 Jul 16.
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The Adriamycin rat/mouse model and its importance to the paediatric surgeon.阿霉素大鼠/小鼠模型及其对小儿外科医生的重要性。
Pediatr Surg Int. 2008 Jan;24(1):113-8. doi: 10.1007/s00383-007-2035-2.
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Doxazolidine induction of apoptosis by a topoisomerase II independent mechanism.多沙唑啶通过一种不依赖拓扑异构酶II的机制诱导细胞凋亡。
J Med Chem. 2007 Sep 6;50(18):4493-500. doi: 10.1021/jm070569b. Epub 2007 Aug 16.
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The role of bioreductive activation of doxorubicin in cytotoxic activity against leukaemia HL60-sensitive cell line and its multidrug-resistant sublines.阿霉素的生物还原激活在对白血病HL60敏感细胞系及其多药耐药亚系的细胞毒性活性中的作用。
Br J Cancer. 2005 Jul 11;93(1):89-97. doi: 10.1038/sj.bjc.6602639.
10
Stability of adriamycin-induced DNA adducts and interstrand crosslinks.阿霉素诱导的DNA加合物和链间交联的稳定性。
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Enzymatic activation and binding of adriamycin to nuclear DNA.阿霉素与核DNA的酶促活化及结合
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Reactions of Adriamycin with haemoglobin. Superoxide dismutase indirectly inhibits reactions of the Adriamycin semiquinone.阿霉素与血红蛋白的反应。超氧化物歧化酶间接抑制阿霉素半醌的反应。
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Methidiumpropyl-EDTA.Fe(II) and DNase I footprinting report different small molecule binding site sizes on DNA.甲基丙基-乙二胺四乙酸铁(II)和脱氧核糖核酸酶I足迹法揭示了DNA上不同的小分子结合位点大小。
Nucleic Acids Res. 1983 Aug 25;11(16):5555-67. doi: 10.1093/nar/11.16.5555.
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Binding of [14C]-adriamycin to cellular macromolecules in vivo.[14C] -阿霉素在体内与细胞大分子的结合
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