GSTDTAP  > 资源环境科学
DOI10.1038/s41467-019-12278-3
Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemia
Herling, Carmen D.1; Abedpour, Nima2,3; Weiss, Jonathan1; Schmitt, Anna1,3,4; Jachimowicz, Ron Daniel1,3,4; Merkel, Olaf1,4; Cartolano, Maria2,3; Oberbeck, Sebastian1,3,4,5; Mayer, Petra1,3,4,5; Berg, Valeska1,4; Thomalla, Daniel1,4; Kutsch, Nadine1; Stiefelhagen, Marius1; Cramer, Paula1; Wendtner, Clemens-Martin6; Persigehl, Thorsten7; Saleh, Andreas8; Altmueller, Janine3,9; Nuernberg, Peter3,4,9; Pallasch, Christian1,3,4; Achter, Viktor10; Lang, Ulrich10,11; Eichhorst, Barbara1; Castiglione, Roberta12; Schaefer, Stephan C.12; Buettner, Reinhard12; Kreuzer, Karl-Anton1; Reinhardt, Hans Christian1,3,4; Hallek, Michael1,3,4; Frenzel, Lukas P.1,4; Peifer, Martin2,3
2019-09-24
发表期刊NATURE COMMUNICATIONS
ISSN2041-1723
出版年2018
卷号9
文章类型Article
语种英语
国家Germany
英文摘要

Deciphering the evolution of cancer cells under therapeutic pressure is a crucial step to understand the mechanisms that lead to treatment resistance. To this end, we analyzed whole-exome sequencing data of eight chronic lymphocytic leukemia (CLL) patients that developed resistance upon BCL2-inhibition by venetoclax. Here, we report recurrent mutations in BTG1 (2 patients) and homozygous deletions affecting CDKN2A/B (3 patients) that developed during treatment, as well as a mutation in BRAF and a high-level focal amplification of CD274 (PD-L1) that might pinpoint molecular aberrations offering structures for further therapeutic interventions.


领域资源环境
收录类别SCI-E
WOS记录号WOS:000425504500004
WOS关键词CELL LUNG-CANCER ; DNA METHYLATION DATA ; RECURRENT MUTATIONS ; RICHTER SYNDROME ; EVOLUTION ; TRANSFORMATION ; PROGRESSION ; SURVIVAL ; PD-L1 ; CD274
WOS类目Multidisciplinary Sciences
WOS研究方向Science & Technology - Other Topics
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文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/204556
专题资源环境科学
作者单位1.Univ Cologne, Ctr Integrated Oncol Cologne Bonn, Dept Internal Med 1, D-50937 Cologne, Germany;
2.Univ Cologne, Ctr Integrated Oncol Cologne Bonn, Dept Translat Genom, Med Fac, D-50931 Cologne, Germany;
3.Univ Cologne, CMMC, D-50931 Cologne, Germany;
4.Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany;
5.Univ Cologne, Lab Lymphocyte Signaling & Oncoproteom, D-50931 Cologne, Germany;
6.Klinikum Schwabing, Dept Hematol Oncol Immunol Palliat Care Infect Di, D-80804 Munich, Germany;
7.Cologne Univ Hosp, Dept Radiol, D-50937 Cologne, Germany;
8.Stadtisches Klinikum Munchen Schwabing, Dept Diagnost & Intervent Radiol & Pediat Radiol, D-80804 Munich, Germany;
9.Univ Cologne, CCG, D-50931 Cologne, Germany;
10.Univ Cologne, Comp Ctr, D-50931 Cologne, Germany;
11.Univ Cologne, Dept Informat, D-50931 Cologne, Germany;
12.Univ Cologne, Dept Pathol, D-50937 Cologne, Germany
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GB/T 7714
Herling, Carmen D.,Abedpour, Nima,Weiss, Jonathan,et al. Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemia[J]. NATURE COMMUNICATIONS,2019,9.
APA Herling, Carmen D..,Abedpour, Nima.,Weiss, Jonathan.,Schmitt, Anna.,Jachimowicz, Ron Daniel.,...&Peifer, Martin.(2019).Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemia.NATURE COMMUNICATIONS,9.
MLA Herling, Carmen D.,et al."Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemia".NATURE COMMUNICATIONS 9(2019).
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