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Targeting the FOXM1/BUB1B signaling network in multiple myeloma: mechanistic insights and therapeutic potential.

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Leukemia & lymphoma 📖 저널 OA 8.2% 2022: 1/1 OA 2025: 2/55 OA 2026: 11/137 OA 2022~2026 2026 Vol.67(5) p. 959-988
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출처

Yasin D, Sami N, Khalid S, Zaheer U, Rasool Z, Faridi F, Asmar M, Uddin S

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Multiple myeloma (MM) is a plasma cell cancer characterized by genomic instability and drug resistance.

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APA Yasin D, Sami N, et al. (2026). Targeting the FOXM1/BUB1B signaling network in multiple myeloma: mechanistic insights and therapeutic potential.. Leukemia & lymphoma, 67(5), 959-988. https://doi.org/10.1080/10428194.2025.2612628
MLA Yasin D, et al.. "Targeting the FOXM1/BUB1B signaling network in multiple myeloma: mechanistic insights and therapeutic potential.." Leukemia & lymphoma, vol. 67, no. 5, 2026, pp. 959-988.
PMID 41578708 ↗

Abstract

Multiple myeloma (MM) is a plasma cell cancer characterized by genomic instability and drug resistance. The FOXM1 transcription factor and the BUB1B kinase are pivotal drivers of this malignancy. FOXM1 promotes cell cycle progression and is upregulated by oncogenic pathways like mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase (PI3K)/AKT, correlating with aggressive disease. BUB1B ensures proper chromosome segregation, and its dysregulation fuels genomic instability. Critically, FOXM1 transcriptionally regulates BUB1B, forming an oncogenic axis that enhances proliferation, drug resistance, and survival. This FOXM1-BUB1B pathway is a promising therapeutic target, with inhibitors under preclinical investigation. Future research must validate its clinical relevance, explore combination therapies, and assess its potential as a biomarker to overcome challenges like toxicity and resistance.

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