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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2010-11-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Culjkovic-Kraljacic, Bijana -- Borden, Katherine L B -- R01 CA080728/CA/NCI NIH HHS/ -- R01 CA098571/CA/NCI NIH HHS/ -- Canadian Institutes of Health Research/Canada -- New York, N.Y. -- Science. 2010 Nov 26;330(6008):1183-4. doi: 10.1126/science.1199405.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Research in Immunology and Cancer, Department of Pathology and Cell Biology, Universite de Montreal, Pavillion Marcelle-Coutu, Chemin Polytechnique, Montreal, QC, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21109655" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; Calcium/*metabolism ; *Calcium Signaling ; Endoplasmic Reticulum/*metabolism ; Inositol 1,4,5-Trisphosphate/metabolism ; Inositol 1,4,5-Trisphosphate Receptors/metabolism ; Intranuclear Space/metabolism ; Mice ; Mitochondria/metabolism ; Nuclear Proteins/*metabolism ; Phosphorylation ; Protein Isoforms/metabolism ; Transcription Factors/*metabolism ; Tumor Suppressor Proteins/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2014-05-30
    Description: Drug resistance is a major hurdle in oncology. Responses of acute myeloid leukaemia (AML) patients to cytarabine (Ara-C)-based therapies are often short lived with a median overall survival of months. Therapies are under development to improve outcomes and include targeting the eukaryotic translation initiation factor (eIF4E) with its inhibitor ribavirin. In a Phase II clinical trial in poor prognosis AML, ribavirin monotherapy yielded promising responses including remissions; however, all patients relapsed. Here we identify a novel form of drug resistance to ribavirin and Ara-C. We observe that the sonic hedgehog transcription factor glioma-associated protein 1 (GLI1) and the UDP glucuronosyltransferase (UGT1A) family of enzymes are elevated in resistant cells. UGT1As add glucuronic acid to many drugs, modifying their activity in diverse tissues. GLI1 alone is sufficient to drive UGT1A-dependent glucuronidation of ribavirin and Ara-C, and thus drug resistance. Resistance is overcome by genetic or pharmacological inhibition of GLI1, revealing a potential strategy to overcome drug resistance in some patients.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138053/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138053/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zahreddine, Hiba Ahmad -- Culjkovic-Kraljacic, Biljana -- Assouline, Sarit -- Gendron, Patrick -- Romeo, Andrea A -- Morris, Stephen J -- Cormack, Gregory -- Jaquith, James B -- Cerchietti, Leandro -- Cocolakis, Eftihia -- Amri, Abdellatif -- Bergeron, Julie -- Leber, Brian -- Becker, Michael W -- Pei, Shanshan -- Jordan, Craig T -- Miller, Wilson H -- Borden, Katherine L B -- R01 80728/PHS HHS/ -- R01 98571/PHS HHS/ -- R01 CA080728/CA/NCI NIH HHS/ -- R01 CA098571/CA/NCI NIH HHS/ -- England -- Nature. 2014 Jul 3;511(7507):90-3. doi: 10.1038/nature13283. Epub 2014 May 28.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Research in Immunology and Cancer and Department of Pathology and Cell Biology, Universite de Montreal, P.O. Box 6128, Downtown Station, Montreal, Quebec H3C 3J7, Canada. ; Segal Cancer Centre, Lady Davis Institute, Jewish General Hospital, McGill University, 3755 Cote-Ste-Catherine Road, Montreal, Quebec H3T 1E2, Canada. ; Pharmascience Inc., 6111 Royalmount Avenue, Montreal, Quebec H4P 2T4, Canada. ; 1] Pharmascience Inc., 6111 Royalmount Avenue, Montreal, Quebec H4P 2T4, Canada [2] JAQJAM Consulting, Montreal J7V 9B6, Canada. ; Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medical College, Cornell University, 1305 York Avenue, New York, New York 10021, USA. ; Hopital Maisonneuve-Rosemont, 5415 Boulevard de l'Assomption, Montreal, Quebec H1T 2M4, Canada. ; McMaster University/Hamilton Health Sciences, 237 Barton Street East, Hamilton, Ontario L8L 2X2, Canada. ; Department of Medicine, Division of Hematology/Oncology, 601 Elmwood Avenue, University of Rochester, Rochester, New York 14627, USA. ; Division of Hematology, Department of Medicine, University of Colorado Denver, 13123 East 16th Avenue, Aurora, Colorado 80045, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24870236" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Line, Tumor ; Cytarabine/metabolism/pharmacology ; *Drug Resistance, Neoplasm/drug effects/genetics ; Gene Deletion ; Glucuronic Acid/*metabolism ; Glucuronosyltransferase/biosynthesis/*metabolism ; Hedgehog Proteins/*metabolism ; Humans ; Leukemia, Myeloid, Acute/*drug therapy/enzymology/*metabolism/pathology ; Ribavirin/metabolism/pharmacology ; Signal Transduction ; Transcription Factors/antagonists & inhibitors/genetics/*metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2013-02-19
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 4
    Publication Date: 2016-05-12
    Description: Regulation of nuclear-cytoplasmic trafficking of oncoproteins is critical for growth homeostasis. Dysregulated trafficking contributes to malignancy, whereas understanding the process can reveal unique therapeutic opportunities. Here, we focus on eukaryotic translation initiation factor 4E (eIF4E), a prooncogenic protein highly elevated in many cancers, including acute myeloid leukemia (AML). Typically, eIF4E...
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 5
    Publication Date: 2013-03-06
    Description: Recognition of the methyl-7-guanosine (m7G) cap structure on mRNA is an essential feature of mRNA metabolism and thus gene expression. Eukaryotic translation initiation factor 4E (eIF4E) promotes translation, mRNA export, proliferation, and oncogenic transformation dependent on this cap-binding activity. eIF4E–cap recognition is mediated via complementary charge interactions of the positively...
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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