JNK1 inhibitors target distal B cell receptor signaling and overcome BTK-inhibitor resistance in CLL

Inhibition of the proximal B cell receptor (BCR) signaling pathway by BTK inhibitors is highly effective in the treatment of CLL, but drug resistance or intolerance occurs. Here, we investigated c-Jun N-terminal protein kinase 1 (JNK1) as an alternative drug target in the distal BCR pathway. JNK1 was preferentially overexpressed and activated in poor prognostic CLL with unmutated IGHV. Proximal BCR inhibition (BTK, PI3K, or SYK inhibitors) or SYK knockdown efficiently dephosphorylated JNK1, identifying JNK1 as a critical BCR downstream kinase in CLL. JNK1 inhibition induced apoptosis in primary CLL cells, resulting in the downregulation of BCL2, MCL1, and c-JUN. JNK1 inhibition in patient-derived CLL xenografted mice and Eµ-TCL1-tg mice prevented CLL progression, reduced splenic infiltration, and restored T cell function and normal hematopoiesis. JNK1 inhibitors even remained effective in ibrutinib refractory CLL. In conclusion, our study revealed JNK1 as a promising drug target in CLL downstream of the BCR, overcoming ibrutinib resistance, blocking the protective microenvironment, and improving CLL-specific immunosuppressive mechanisms.

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Publication Details

Journal
The Journal of Experimental Medicine
Published
2024-11-21
DOI
https://doi.org/10.1084/jem.20230681
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
0.00

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article

JNK1 inhibitors target distal B cell receptor signaling and overcome BTK-inhibitor resistance in CLL

Claudia Wickenhauser, Sandra Kissel, Christine Dierks, Marco Herling et al.
The Journal of Experimental Medicine
Chronic Lymphocytic Leukemia Research
article

JNK1 inhibitors target distal B cell receptor signaling and overcome BTK-inhibitor resistance in CLL

Claudia Wickenhauser, Sandra Kissel, Christine Dierks, Marco Herling, Konrad Aumann, Daniela Bräuer-Hartmann, Marie Follo, Nimitha R. Mathew, Oleksandra Skorobohatko, Marcus Bauer, Sarah Decker, Dmitry Chernyakov, Shifa Khaja Saleem, C. L. Schmidt, Claudius Klein
article en

Abstract

Inhibition of the proximal B cell receptor (BCR) signaling pathway by BTK inhibitors is highly effective in the treatment of CLL, but drug resistance or intolerance occurs. Here, we investigated c-Jun N-terminal protein kinase 1 (JNK1) as an alternative drug target in the distal BCR pathway. JNK1 was preferentially overexpressed and activated in poor prognostic CLL with unmutated IGHV. Proximal BCR inhibition (BTK, PI3K, or SYK inhibitors) or SYK knockdown efficiently dephosphorylated JNK1, identifying JNK1 as a critical BCR downstream kinase in CLL. JNK1 inhibition induced apoptosis in primary CLL cells, resulting in the downregulation of BCL2, MCL1, and c-JUN. JNK1 inhibition in patient-derived CLL xenografted mice and Eµ-TCL1-tg mice prevented CLL progression, reduced splenic infiltration, and restored T cell function and normal hematopoiesis. JNK1 inhibitors even remained effective in ibrutinib refractory CLL. In conclusion, our study revealed JNK1 as a promising drug target in CLL downstream of the BCR, overcoming ibrutinib resistance, blocking the protective microenvironment, and improving CLL-specific immunosuppressive mechanisms.

The Journal of Experimental MedicineVol. 222(1)
University of Freiburg (DE), University Medical Center (US), Martin Luther University Halle-Wittenberg (DE)
Deutsche Forschungsgemeinschaft, Albert-Ludwigs-Universität Freiburg, José Carreras Leukämie-Stiftung, Deutsche Krebshilfe, Medizinische Fakultät der Albert-Ludwigs-Universität Freiburg
Good health and well-being
Openalex Percentile: Top 63%
Chronic Lymphocytic Leukemia Research
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