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本文引用的文献

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JCSM Rapid Commun. 2019 Jan-Jun;2(1).
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The triangle of death of neurons: Oxidative damage, mitochondrial dysfunction, and loss of choline-containing biomolecules in brains of mice treated with doxorubicin. Advanced insights into mechanisms of chemotherapy induced cognitive impairment ("chemobrain") involving TNF-α.神经元的死亡三角:阿霉素处理的小鼠大脑中的氧化损伤、线粒体功能障碍和含胆碱生物分子的丧失。涉及 TNF-α 的化疗引起的认知障碍(“化疗脑”)的机制的深入了解。
Free Radic Biol Med. 2019 Apr;134:1-8. doi: 10.1016/j.freeradbiomed.2018.12.029. Epub 2018 Dec 26.
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Chemotherapy-induced muscle wasting: association with NF-κB and cancer cachexia.化疗诱导的肌肉萎缩:与核因子κB及癌症恶病质的关联
Eur J Transl Myol. 2018 Jun 6;28(2):7590. doi: 10.4081/ejtm.2018.7590. eCollection 2018 Apr 24.
4
Loss of skeletal muscle during systemic chemotherapy is prognostic of poor survival in patients with foregut cancer.全身化疗期间骨骼肌丢失是前肠癌患者预后不良的预测因素。
J Cachexia Sarcopenia Muscle. 2018 Apr;9(2):315-325. doi: 10.1002/jcsm.12267. Epub 2018 Jan 9.
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Pain in Platin-Induced Neuropathies: A Systematic Review and Meta-Analysis.铂类诱导的神经病变中的疼痛:一项系统评价和荟萃分析
Pain Ther. 2018 Jun;7(1):105-119. doi: 10.1007/s40122-017-0092-3. Epub 2017 Dec 1.
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Susceptibility of different mouse strains to oxaliplatin peripheral neurotoxicity: Phenotypic and genotypic insights.不同小鼠品系对奥沙利铂周围神经毒性的易感性:表型和基因型见解。
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7
Shortwave infrared luminescent Pt-nanowires: a mechanistic study of emission in solution and in the solid state.短波红外发光铂纳米线:溶液和固态中发射的机理研究
Dalton Trans. 2017 Oct 10;46(39):13562-13581. doi: 10.1039/c7dt02317k.
8
CNS Demyelination with TNF-α Blockers.使用肿瘤坏死因子-α阻滞剂导致的中枢神经系统脱髓鞘病变
Curr Neurol Neurosci Rep. 2017 Apr;17(4):36. doi: 10.1007/s11910-017-0742-1.
9
Dysregulation of cytokine mediated chemotherapy induced cognitive impairment.细胞因子介导的化疗诱导认知障碍的失调。
Pharmacol Res. 2017 Mar;117:267-273. doi: 10.1016/j.phrs.2017.01.001. Epub 2017 Jan 4.
10
Imaging of radicals following injury or acute stress in peripheral nerves with activatable fluorescent probes.使用可激活荧光探针对外周神经损伤或急性应激后的自由基进行成像。
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新型体外高细胞毒性铂和钯氰氧基配合物,体内副作用极小。

New in vitro highly cytotoxic platinum and palladium cyanoximates with minimal side effects in vivo.

机构信息

Department of Chemistry, Temple Hall 431, Missouri State University, 901 S. National, Springfield, MO 65897, USA.

Department of Biology, Missouri State University, MC/Center for Biomedical & Life Sciences, Springfield, MO 65897, USA.

出版信息

J Inorg Biochem. 2020 Jul;208:111082. doi: 10.1016/j.jinorgbio.2020.111082. Epub 2020 May 6.

DOI:10.1016/j.jinorgbio.2020.111082
PMID:32413634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7518941/
Abstract

Several biologically active bivalent Pd and Pt complexes with two structurally similar cyanoxime ligands abbreviated as H(DECO): 2-oximino-2-cyano-N,N'-diethylacetamide, and H(PyrCO): 2-oximino-2-cyan-N-pyrrolidine acetamide were synthesized and characterized using spectroscopic methods, thermal analysis and X-ray crystallography. Structures revealed planar cis-geometry of studied complexes. Freshly obtained Pt(DECO), Pd(DECO), Pt(PyrCO) and Pd(PyrCO) complexes were used in for in vitro cytotoxicity assays using two different etiology human cancer cell lines HeLa and WiDr cells. Investigated compounds showed cytotoxicity levels at or above cisplatin. Pt(DECO) was also tested in vivo in healthy C57BL/6 mice. The complex was administered at three different dosage (0, 7.5, 15 mg/kg, i.p. once/week), over a total period of 8 weeks. No changes were observed in the animal weight in the treated mice compared to the control dextrose-treated group. The levels of erythrocytes, leukocytes, and hemoglobin were within the normal level suggesting low myelotoxicity. Negligible cardiotoxicity was observed from the histological evaluation of the hearts from the treated animals. Results from the tail nerve conduction velocity (NCV) and nerve histomorphometry suggested no impact of Pt(DECO) on peripheral nerves. The complex, however, induced certain hepatotoxicity and lead to the elevation of IL-6, a pro-inflammatory cytokine. Overall, Pt(DECO)2 showed minimal in vivo toxicity, thus presenting a promising candidate for future testing in animal models of cancer.

摘要

几种具有两个结构相似的氰肟配体的生物活性双价 Pd 和 Pt 配合物,缩写为 H(DECO):2-肟基-2-氰基-N,N'-二乙酰胺和 H(PyrCO):2-肟基-2-氰基-N-吡咯烷乙酰胺,已通过光谱法、热分析和 X 射线晶体学进行了合成和表征。结构揭示了研究配合物的平面顺式几何形状。新获得的 Pt(DECO)、Pd(DECO)、Pt(PyrCO)和 Pd(PyrCO)配合物用于使用两种不同病因的人类癌细胞系 HeLa 和 WiDr 细胞进行体外细胞毒性测定。研究的化合物表现出与顺铂相当或更高的细胞毒性水平。Pt(DECO)也在健康 C57BL/6 小鼠体内进行了测试。该复合物以三种不同剂量(0、7.5、15mg/kg,腹腔注射,每周一次)给药,总共 8 周。与对照葡萄糖处理组相比,治疗小鼠的动物体重没有变化。红细胞、白细胞和血红蛋白水平均在正常范围内,表明骨髓毒性较低。从治疗动物的心脏组织学评估中观察到可忽略不计的心脏毒性。尾部神经传导速度 (NCV) 和神经形态计量学的结果表明,Pt(DECO)对周围神经没有影响。然而,该复合物会引起一定的肝毒性,并导致促炎细胞因子 IL-6 的升高。总的来说,Pt(DECO)2 表现出最小的体内毒性,因此是未来在癌症动物模型中进行测试的有前途的候选物。