Dual CARM1-and IKZF3-targeting: A novel approach to multiple myeloma therapy

Advancements in the treatment of multiple myeloma (MM) have resulted in an improvement in the survival rate. However, there continues to be an urgent need for improved therapies. The protein arginine methyltransferase, CARM1 (coactivator associated arginine methyltransferase 1), is emerging as a potential cancer therapy target and inhibitors have been developed. MM cell lines are particularly dependent on CARM1 for cell survival. Here, we show that targeting of CARM1 through small molecule inhibition potentiates the activity of immunomodulatory drugs (IMiDs) in cell line models of MM. This likely occurs through synergistic targeting of Aiolos (IKZF3) and MYC expression. Rational design of a new molecule, 074, which consists of a CARM1 inhibitor linked to the IMiD pomalidomide, was carried out and treatment with this agent led to more potent killing of MM cells than either the CARM1 inhibitor or the IMiD as single agents. Importantly, 074 was able to override IMiD resistance. Taken together, our results demonstrate that dual CARM1/IKZF3-targeting agents represent a promising novel therapeutic strategy for MM and IMiD-resistant disease.

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Publication Details

Journal
Molecular Therapy Oncology
Published
2025-02-20
DOI
https://doi.org/10.1016/j.omton.2025.200952
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00

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article

Dual CARM1-and IKZF3-targeting: A novel approach to multiple myeloma therapy

Basudev Chowdhury, Katherine A. Donovan, Swati Garg, Xiaoxi Liu et al.
Molecular Therapy Oncology
Protein Degradation and Inhibitors
article

Dual CARM1-and IKZF3-targeting: A novel approach to multiple myeloma therapy

Basudev Chowdhury, Katherine A. Donovan, Swati Garg, Xiaoxi Liu, Cara Ann Starnbach, Maria Tarazona Guzman, Martin Sattler, James D. Griffin, Ellen Weisberg, Chengcheng Meng, Richard Maury Stone, Dana Sanchez, Jun Qi, Sara J. Buhrlage, Wei Pin Teh, Taisei Akatsu, Michelle Wang, Wei Ni
article en

Abstract

Advancements in the treatment of multiple myeloma (MM) have resulted in an improvement in the survival rate. However, there continues to be an urgent need for improved therapies. The protein arginine methyltransferase, CARM1 (coactivator associated arginine methyltransferase 1), is emerging as a potential cancer therapy target and inhibitors have been developed. MM cell lines are particularly dependent on CARM1 for cell survival. Here, we show that targeting of CARM1 through small molecule inhibition potentiates the activity of immunomodulatory drugs (IMiDs) in cell line models of MM. This likely occurs through synergistic targeting of Aiolos (IKZF3) and MYC expression. Rational design of a new molecule, 074, which consists of a CARM1 inhibitor linked to the IMiD pomalidomide, was carried out and treatment with this agent led to more potent killing of MM cells than either the CARM1 inhibitor or the IMiD as single agents. Importantly, 074 was able to override IMiD resistance. Taken together, our results demonstrate that dual CARM1/IKZF3-targeting agents represent a promising novel therapeutic strategy for MM and IMiD-resistant disease.

Molecular Therapy OncologyVol. 33(1)
Harvard University (US), Dana-Farber Cancer Institute (US)
Foundation for the National Institutes of Health, Eli Lilly and Company, Takeda Pharmaceuticals U.S.A., National Institutes of Health
Openalex Percentile: Top 97%
Protein Degradation and Inhibitors
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