التفاصيل البيبلوغرافية
| العنوان: |
Nucleolus and c-Myc: potential targets of cardenolide-mediated antitumor activity. |
| المؤلفون: |
Mijatovic, Tatjana, De Nève, Nancy, Gailly, Philippe, Mathieu, Véronique, Haibe-Kains, Benjamin, Bontempi, Gianluca, Lapeira, Javier, Decaestecker, Christine, Facchini, Vincenzo, Kiss, Robert |
| المصدر: |
Molecular cancer therapeutics, 7 (5 |
| سنة النشر: |
2008 |
| المجموعة: |
DI-fusion : dépôt institutionnel de l'Université libre de Bruxelles (ULB) |
| مصطلحات موضوعية: |
Sciences bio-médicales et agricoles, Animals, Antineoplastic Agents -- therapeutic use, Apoptosis, Calcium -- metabolism, Cardenolides -- therapeutic use, Cell Nucleolus -- drug effects, Cell Nucleolus -- ultrastructure, Cell Proliferation, Down-Regulation, Humans, Male, Mice, Prostatic Neoplasms -- drug therapy, Prostatic Neoplasms -- metabolism, Prostatic Neoplasms -- ultrastructure, Proto-Oncogene Proteins c-myc -- genetics, Proto-Oncogene Proteins c-myc -- metabolism, Tumor Cells, Cultured |
| الوصف: |
The use of cardenolides like ouabain, digitoxin, or oleandrin has been reported previously many times as a means of potentially combating human refractory prostate cancer by inducing apoptosis through an increase in intracellular calcium concentrations. The aims of the current study were to investigate if part of the antitumor effects mediated by cardenolides concerned disorganization of nucleolar structure and whether this was further associated with a marked decrease in c-Myc expression. Accordingly, the antitumor activity of a novel hemisynthetic cardenolide [1R,3aS,3bR,5aS,6aR,7aS,9R,12aR,13aR,15aR]-3a,11a-dihydroxy-13a-(hydroxymethyl)-9,15a-dimethyl-1-(5-oxo-2,5-dihydrofuran-3-yl)icosahydro-1H,4'H-spiro[cyclopenta [7,8]phenanthro[2,3-b]pyrano[3,2-e][1,4]dioxine-11,2'-[1,3]thiazolidin]-4'-one (UNBS1450)] was compared with that of classic cardenolides and reference anticancer agents in prostate cancer cell lines in vitro and in vivo following s.c. and orthotopic prostate cancer cell grafting into mice. The present study indicates that UNBS1450 markedly decreases the in vitro viability/proliferation of human prostate cancer cell lines but not of normal cells. The induced effects are not linked to an increase in intracellular calcium concentrations and subsequent induction of apoptosis. Rather, they appear to relate to the compound's capacity to disorganize nucleolar structure and function (through an impairment of cyclin-dependent kinase and c-Myc expression and related signaling pathways; paralleled by the disorganization of cancer cell-specific perinucleolar bodies as revealed by disruption of Sam68). This nonapoptotic cancer cell death mediated by severe nucleolar targeting and down-regulation of c-Myc expression is a completely new cardenolide-induced mechanism of antitumor action. ; Journal Article ; Research Support, Non-U.S. Gov't ; info:eu-repo/semantics/published |
| نوع الوثيقة: |
article in journal/newspaper |
| وصف الملف: |
1 full-text file(s): application/pdf |
| اللغة: |
English |
| العلاقة: |
uri/info:doi/10.1158/1535-7163.MCT-07-2241; uri/info:pii/7/5/1285; uri/info:pmid/18483316; uri/info:scp/49849100632; https://dipot.ulb.ac.be/dspace/bitstream/2013/52071/3/doi_27240.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/52071Test |
| الإتاحة: |
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/52071Test |
| رقم الانضمام: |
edsbas.980D1B7C |
| قاعدة البيانات: |
BASE |
