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An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro
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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491352/ https://www.ncbi.nlm.nih.gov/pubmed/36320328 http://dx.doi.org/10.1039/d2md00144f |
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author | Abodo Onambele, Liliane Hoffmann, Natalie Kater, Lisa Hemmersbach, Lars Neudörfl, Jörg-Martin Sitnikov, Nikolay Kater, Benjamin Frias, Corazon Schmalz, Hans-Günther Prokop, Aram |
author_facet | Abodo Onambele, Liliane Hoffmann, Natalie Kater, Lisa Hemmersbach, Lars Neudörfl, Jörg-Martin Sitnikov, Nikolay Kater, Benjamin Frias, Corazon Schmalz, Hans-Günther Prokop, Aram |
author_sort | Abodo Onambele, Liliane |
collection | PubMed |
description | 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 in vitro. 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 via 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 via western blot showed an upregulation of the proapoptotic protein harakiri by 9%. |
format | Online Article Text |
id | pubmed-9491352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-94913522022-10-31 An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro Abodo Onambele, Liliane Hoffmann, Natalie Kater, Lisa Hemmersbach, Lars Neudörfl, Jörg-Martin Sitnikov, Nikolay Kater, Benjamin Frias, Corazon Schmalz, Hans-Günther Prokop, Aram RSC Med Chem Chemistry 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 in vitro. 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 via 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 via western blot showed an upregulation of the proapoptotic protein harakiri by 9%. RSC 2022-06-30 /pmc/articles/PMC9491352/ /pubmed/36320328 http://dx.doi.org/10.1039/d2md00144f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Abodo Onambele, Liliane Hoffmann, Natalie Kater, Lisa Hemmersbach, Lars Neudörfl, Jörg-Martin Sitnikov, Nikolay Kater, Benjamin Frias, Corazon Schmalz, Hans-Günther Prokop, Aram An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
title | An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
title_full | An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
title_fullStr | An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
title_full_unstemmed | An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
title_short | An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
title_sort | organometallic analogue of combretastatin a-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491352/ https://www.ncbi.nlm.nih.gov/pubmed/36320328 http://dx.doi.org/10.1039/d2md00144f |
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