Cell cycle phase perturbations and apoptosis in tumour cells induced by aplidine

التفاصيل البيبلوغرافية
العنوان: Cell cycle phase perturbations and apoptosis in tumour cells induced by aplidine
المؤلفون: Eugenio Erba, Jose Jimeno, I Muradore, Giovanna Chiorino, L Bassano, Paolo Ubezio, G Di Liberti, Maria Alfonsina Desiderio, A.M. Codegoni, Maurizio D'Incalci, Sara Vignati, Glynn Faircloth
المصدر: British Journal of Cancer
بيانات النشر: Nature Publishing Group, 2002.
سنة النشر: 2002
مصطلحات موضوعية: Cancer Research, Programmed cell death, Aplidine, Antineoplastic Agents, Biology, Peptides, Cyclic, Cell cycle phase, natural compound, Depsipeptides, medicine, Putrescine, Tumor Cells, Cultured, Humans, Experimental Therapeutics, Cytotoxicity, Depsipeptide, Leukemia, Kinase, Cell Cycle, apoptosis, Cell cycle, Cell biology, Oncology, Mechanism of action, Apoptosis, Immunology, medicine.symptom
الوصف: Aplidine, dehydrodidemnin B, is a marine depsipeptide isolated from the Mediterranean tunicate Aplidium albicans currently in phase II clinical trial. In human Molt-4 leukaemia cells Aplidine was found to be cytotoxic at nanomolar concentrations and to induce both a G1 arrest and a G2 blockade. The drug-induced cell cycle perturbations and subsequent cell death do not appear to be related to macromolecular synthesis (protein, RNA, DNA) since the effects occur at concentrations (e.g. 10 nM) in which macromolecule synthesis was not markedly affected. Ten nM Aplidine for 1 h inhibited ornithine decarboxylase activity, with a subsequently strong decrease in putrescine levels. This finding has questionable relevance since addition of putrescine did not significantly reduce the cell cycle perturbations or the cytotoxicity of Aplidine. The cell cycle perturbations caused by Aplidine were also not due to an effect on the cyclin-dependent kinases. Although the mechanism of action of Aplidine is still unclear, the cell cycle phase perturbations and the rapid induction of apoptosis in Molt-4 cells appear to be due to a mechanism different from that of known anticancer drugs. British Journal of Cancer (2002) 86, 1510–1517. DOI: 10.1038/sj/bjc/6600265 www.bjcancer.com © 2002 Cancer Research UK
اللغة: English
تدمد: 1532-1827
0007-0920
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e7bbcdb2d255e5e233deab16fb810c0Test
http://europepmc.org/articles/PMC2375382Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....5e7bbcdb2d255e5e233deab16fb810c0
قاعدة البيانات: OpenAIRE