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一种康普他汀A - 4的有机金属类似物及其对淋巴瘤、白血病和其他肿瘤细胞的凋亡诱导作用。

An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells .

作者信息

Abodo Onambele Liliane, Hoffmann Natalie, Kater Lisa, Hemmersbach Lars, Neudörfl Jörg-Martin, Sitnikov Nikolay, Kater Benjamin, Frias Corazon, Schmalz Hans-Günther, Prokop Aram

机构信息

Department of Pediatric Oncology/Hematology, Children's Hospital of the City of Cologne Amsterdamer Str. 59 50735 Cologne Germany.

Department of Pediatric Oncology/Hematology, University Medical Center Charité Campus Virchow, Augustenburger Pl. 1 13353 Berlin Germany.

出版信息

RSC Med Chem. 2022 Jun 30;13(9):1044-1051. doi: 10.1039/d2md00144f. eCollection 2022 Sep 21.

Abstract

Hexacarbonyl[1,3-dimethoxy-5-((4'-methoxyphenyl)ethynyl)benzene]dicobalt (NAHO27), an organometallic analogue of combretastatin A-4, has been synthesized and its activity against lymphoma, leukemia, breast cancer and melanoma cells has been investigated. It was shown that NAHO27 specifically induces apoptosis in BJAB lymphoma and Nalm-6 leukemia cells at low micromolar concentration and does not affect normal leukocytes . It also proved to be active against vincristine and daunorubicin resistant leukemia cell lines with p-glycoprotein-caused multidrug resistance and showed a pronounced (550%) synergistic effect when co-applied with vincristine at very low concentrations. Mechanistic investigations revealed NAHO27 to induce apoptosis the mitochondrial (intrinsic) pathway as reflected by the processing of caspases 3 and 9, the involvement of Bcl-2 and smac/DIABLO, and the reduction of mitochondrial membrane potential. Gene expression analysis and protein expression analysis western blot showed an upregulation of the proapoptotic protein harakiri by 9%.

摘要

六羰基[1,3 - 二甲氧基 - 5 - ((4'-甲氧基苯基)乙炔基)苯]二钴(NAHO27),一种康普他汀A - 4的有机金属类似物,已被合成,并对其针对淋巴瘤、白血病、乳腺癌和黑色素瘤细胞的活性进行了研究。结果表明,NAHO27在低微摩尔浓度下能特异性诱导BJAB淋巴瘤细胞和Nalm - 6白血病细胞凋亡,且不影响正常白细胞。它还被证明对由P - 糖蛋白引起多药耐药的长春新碱和柔红霉素耐药白血病细胞系有活性,并且在极低浓度下与长春新碱共同应用时显示出显著的(550%)协同效应。机制研究表明,NAHO27通过半胱天冬酶3和9的加工、Bcl - 2和smac/DIABLO的参与以及线粒体膜电位的降低,诱导线粒体(内在)凋亡途径。基因表达分析和蛋白质表达分析 - 蛋白质印迹显示促凋亡蛋白harakiri上调了9%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d8/9491352/e641a127521a/d2md00144f-f1.jpg

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