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Dysregulation of FBW7 in malignant lymphoproliferative disorders

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FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.988138

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FBW7; lymphoproliferative disorders; ubiquitin; Notch; c-Myc

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  1. Science and Technology Agency of Jilin province
  2. [20200201591JC]

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This review focuses on the functions, substrates, and expression of FBW7 in malignant lymphoproliferative disorders. FBW7, as a key component of UPS proteins and a critical tumor suppressor, plays an important role in controlling protein degradation and the development of various cancers.
The ubiquitin-proteasome system (UPS) is involved in various aspects of cell processes, including cell proliferation, differentiation, and cell cycle progression. F-box and WD repeat domain-containing protein 7 (FBW7), as a key component of UPS proteins and a critical tumor suppressor in human cancers, controls proteasome-mediated degradation by ubiquitinating oncoproteins such as c-Myc, Mcl-1, cyclin E, and Notch. It also plays a role in the development of various cancers, including solid and hematological malignancies, such as T-cell acute lymphoblastic leukemia, diffuse large B-cell lymphoma, and multiple myeloma. This comprehensive review emphasizes the functions, substrates, and expression of FBW7 in malignant lymphoproliferative disorders.

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