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The master regulator FUBP1: its emerging role in normal cell function and malignant development
Lydie Debaize1, Marie-Bérengère Troadec2,3,4
1Univ Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, F-35000, Rennes, France.
Abstract:
The human Far Upstream Element (FUSE) Binding Protein 1 (FUBP1) is a multifunctional DNA- and RNA-binding protein involved in diverse cellular processes. FUBP1 is a master regulator of transcription, translation, and RNA splicing. FUBP1 has been identified as a potent pro-proliferative and anti-apoptotic factor by modulation of complex networks. FUBP1 is also described either as an oncoprotein or a tumor suppressor. Especially, FUBP1 overexpression is observed in a growing number of cancer and leads to a deregulation of targets that includes the fine-tuned MYC oncogene. Moreover, recent loss-of-function analyses of FUBP1 establish its essential functions in hematopoietic stem cell maintenance and survival. Therefore, FUBP1 appears as an emerging suspect in hematologic disorders in addition to solid tumors. The scope of the present review is to describe the advances in our understanding of the molecular basis of FUBP1 functions in normal cells and carcinogenesis. We also delineate the recent progresses in the understanding of the master role of FUBP1 in normal and pathological hematopoiesis. We conclude that FUBP1 is not only worth studying biologically but is also of clinical relevance through its pivotal role in regulating multiple cellular processes and its involvement in oncogenesis.
Insights
Far Upstream Element Binding Protein 1 (FUBP1) is a key regulator in cellular processes, impacting both cancer and blood cell development. Understanding FUBP1
Area of Science:
- Molecular Biology
- Cancer Research
- Hematology
Background:
- Far Upstream Element Binding Protein 1 (FUBP1) is a multifunctional DNA/RNA-binding protein.
- It acts as a master regulator of transcription, translation, and RNA splicing.
- FUBP1 has dual roles, acting as both a pro-proliferative factor and potentially a tumor suppressor.
Purpose of the Study:
- To review advances in understanding FUBP1's molecular functions in normal cells and cancer.
- To explore FUBP1's role in normal and pathological hematopoiesis.
- To highlight FUBP1's clinical relevance in oncogenesis and hematologic disorders.
Main Methods:
- Literature review of FUBP1 functions.
- Analysis of FUBP1's role in gene regulation.
- Examination of FUBP1's involvement in cellular proliferation and apoptosis.
Main Results:
- FUBP1 overexpression is linked to various cancers, including deregulation of MYC.
- Loss-of-function studies reveal FUBP1's essential role in hematopoietic stem cell maintenance.
- FUBP1 is implicated in both solid tumors and hematologic disorders.
Conclusions:
- FUBP1 is a critical regulator with significant biological and clinical implications.
- Its multifaceted roles in cellular processes and disease warrant further investigation.
- FUBP1 represents a promising target for therapeutic interventions in cancer and hematologic conditions.
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