(Translated by https://www.hiragana.jp/)
author:"Eichhorst, B." - Search Results - DKFZ
DKFZ 8 records found  Search took 0.00 seconds. 
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[DKFZ-2022-02881] Journal Article
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Deregulation and epigenetic modification of BCL2-family genes cause resistance to venetoclax in hematologic malignancies.
Blood 140(20), 2113 - 2126 () [10.1182/blood.2021014304]  GO
The BCL2 inhibitor venetoclax has been approved to treat different hematological malignancies. Because there is no common genetic alteration causing resistance to venetoclax in chronic lymphocytic leukemia (CLL) and B-cell lymphoma, we asked if epigenetic events might be involved in venetoclax resistance. [...]
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DBCoverage [DKFZ-2021-02076] Journal Article
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Multi-platform profiling characterizes molecular subgroups and resistance networks in chronic lymphocytic leukemia.
Knowledge of the genomic landscape of chronic lymphocytic leukemia (CLL) grows increasingly detailed, providing challenges in contextualizing the accumulated information. To define the underlying networks, we here perform a multi-platform molecular characterization. [...]
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pmc [DKFZ-2019-02309] Journal Article
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Short telomeres are associated with inferior outcome, genomic complexity, and clonal evolution in chronic lymphocytic leukemia.
Leukemia 33(9), 2183 - 2194 () [10.1038/s41375-019-0446-4]  GO
Telomere length in chronic lymphocytic leukemia (CLL) has been shown to be of prognostic importance, but the analyses have largely been executed on heterogeneous patient cohorts outside of clinical trials. In the present study, we performed a comprehensive analysis of telomere length associations in the well characterized CLL8 trial (n = 620) of the German CLL study group, with validation in a representative cohort of the CLL4 trial (n = 293). [...]
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[DKFZ-2019-01842] Journal Article
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Oxidative stress as candidate therapeutic target to overcome microenvironmental protection of CLL.
Leukemia 34(1), 115-127 () [10.1038/s41375-019-0513-x]  GO
Chronic lymphocytic leukemia (CLL) cells depend on microenvironmental non-malignant cells for survival. We compared the transcriptomes of primary CLL cells cocultured or not with protective bone marrow stromal cells (BMSCs) and found that oxidative phosphorylation, mitochondrial function, and hypoxic signaling undergo most significant dysregulation in non-protected CLL cells, with the changes peaking at 6-8 h, directly before induction of apoptosis. [...]
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[DKFZ-2018-00048] Journal Article
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NFATC1 activation by DNA hypomethylation in chronic lymphocytic leukemia correlates with clinical staging and can be inhibited by ibrutinib.
B cell receptor (BCR) signaling is a key for survival of chronic lymphocytic leukemia (CLL) cells, and BCR signaling inhibitors are clinically active. However, relapse and resistance to treatment require novel treatment options. [...]

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