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Verfasst von:Knudsen, Peter Boldsen [VerfasserIn]   i
 Hanna, Bola [VerfasserIn]   i
 Ohl, S. [VerfasserIn]   i
 Sellner, Leopold [VerfasserIn]   i
 Zenz, Thorsten [VerfasserIn]   i
 Döhner, H. [VerfasserIn]   i
 Stilgenbauer, S. [VerfasserIn]   i
 Larsen, T. O. [VerfasserIn]   i
 Lichter, Peter [VerfasserIn]   i
 Seiffert, Moritz [VerfasserIn]   i
Titel:Chaetoglobosin A preferentially induces apoptosis in chronic lymphocytic leukemia cells by targeting the cytoskeleton
Verf.angabe:P.B. Knudsen, B. Hanna, S. Ohl, L. Sellner, T. Zenz, H. Döhner, S. Stilgenbauer, T.O. Larsen, P. Lichter and M. Seiffert
E-Jahr:2014
Jahr:10 January 2014
Umfang:10 S.
Fussnoten:Gesehen am 17.08.2020
Titel Quelle:Enthalten in: Leukemia
Ort Quelle:London : Springer Nature, 1997
Jahr Quelle:2014
Band/Heft Quelle:28(2014), 6, Seite 1289-1298
ISSN Quelle:1476-5551
Abstract:Chronic lymphocytic leukemia (CLL) is an incurable malignancy of mature B cells. One of the major challenges in treatment of CLL is the achievement of a complete remission to prevent relapse of disease originating from cells within lymphoid tissues and subsequent chemoresistance. In search for novel drugs that target CLL cells in protective microenvironments, we performed a fungal extract screen using cocultures of primary CLL cells with bone marrow-derived stromal cells. A secondary metabolite produced by Penicillium aquamarinium was identified as Chaetoglobosin A (ChA), a member of the cytochalasan family that showed preferential induction of apoptosis in CLL cells, even under culture conditions that mimic lymphoid tissues. In vitro testing of 89 CLL cases revealed effective targeting of CLL cells by ChA, independent of bad prognosis characteristics, like 17p deletion or TP53 mutation. To provide insight into its mechanism of action, we showed that ChA targets filamentous actin in CLL cells and thereby induces cell-cycle arrest and inhibits membrane ruffling and cell migration. Our data further revealed that ChA prevents CLL cell activation and sensitizes them for treatment with PI3K and BTK inhibitors, suggesting this compound as a novel potential drug for CLL.
DOI:doi:10.1038/leu.2013.360
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1038/leu.2013.360
 Volltext: https://www.nature.com/articles/leu2013360
 DOI: https://doi.org/10.1038/leu.2013.360
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1727161912
Verknüpfungen:→ Zeitschrift

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