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Updated: Aug 5, 2025

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
RETRACTED: Tyrosine Kinase Inhibitors Target B Lymphocytes
Nikki Lyn Esnardo Upfold1, Pavlo Petakh2,3, Aleksandr Kamyshnyi3
1Department of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology (NTNU), 7028 Trondheim, Norway.
Certain protein kinase inhibitors approved for lung cancer show potential for targeting B lymphocytes, which are implicated in autoimmune diseases and blood cancers. Ceritinib and entrectinib effectively eliminated plasma cells, while others inhibited B cell proliferation.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- B lymphocyte dysfunction underlies autoimmune disorders and blood cancers like multiple myeloma, lymphoma, and leukemia.
- Targeting B cells is crucial for developing new therapies for these conditions.
- Existing drugs for anaplastic lymphoma kinase (ALK)-positive lung cancer may offer novel therapeutic avenues.
Purpose of the Study:
- To investigate the efficacy of ALK inhibitors in targeting leukocyte tyrosine kinase (LTK)-positive B lymphocytes, including antibody-secreting plasma cells.
- To evaluate the potential of these inhibitors as a new treatment strategy for B cell-related autoimmune diseases and blood cancers.
Main Methods:
- Isolated CD19-positive human B cells from healthy donors.
- Stimulated B cell maturation into plasma cells using two distinct methods.
- Assessed cell proliferation and used flow cytometry to analyze treatment effects.
Main Results:
- Ceritinib and entrectinib demonstrated efficacy in eliminating plasma cells from B cell populations.
- Alectinib, brigatinib, and crizotinib inhibited B cell proliferation.
- Lorlatinib exhibited minimal or no effect on B cell populations.
Conclusions:
- Several protein kinase inhibitors approved for ALK-positive lung cancer can effectively target LTK-positive B cells.
- Ceritinib and entrectinib show promise for eliminating plasma cells, suggesting potential applications in treating B cell-mediated autoimmune conditions and cancers.
- These findings open new possibilities for repurposing existing cancer drugs for hematological malignancies and autoimmune disorders.
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