Related Experiment Video
Updated: Dec 27, 2025

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells
Published on: January 20, 2019
MYC's Fine Line Between B Cell Development and Malignancy
Oriol de Barrios1, Ainara Meler1, Maribel Parra1
1Lymphocyte Development and Disease Group, Josep Carreras Leukaemia Research Institute, IJC Building, Campus ICO-Germans Trias i Pujol, Ctra de Can Ruti, 08916 Barcelona, Spain.
Insights
The MYC gene is crucial for B cell development but its dysregulation drives leukemia and lymphoma. Understanding MYC
Area of Science:
- Immunology
- Molecular Biology
- Oncology
Background:
- The transcription factor MYC plays a critical role in B lymphocyte development.
- Proper MYC expression modulation is vital for B cell differentiation stages.
- MYC is a proto-oncogene implicated in various hematological malignancies.
Purpose of the Study:
- To review the role of MYC in B cell development.
- To explore the oncogenic functions of MYC in hematological cancers.
- To highlight the significance of MYC regulatory circuits.
Main Methods:
- Literature review of MYC's function in B cell biology.
- Analysis of MYC's role in oncogenesis.
- Examination of MYC overexpression mechanisms in leukemia and lymphoma.
Main Results:
- MYC is transiently expressed during B cell development, with basal levels maintained until terminal differentiation.
- Aberrant MYC expression in leukemia and lymphoma leads to uncontrolled proliferation and blocked differentiation.
- Overexpression of MYC in these cancers is primarily due to gene amplification, translocations, and transcriptional dysregulation.
Conclusions:
- MYC's precise regulation is essential for normal B cell development.
- Dysregulated MYC is a key driver of B cell malignancies.
- Understanding MYC's regulatory circuitry is crucial for therapeutic strategies in leukemia and lymphoma.
Abstract:
The transcription factor MYC is transiently expressed during B lymphocyte development, and its correct modulation is essential in defined developmental transitions. Although temporary downregulation of MYC is essential at specific points, basal levels of expression are maintained, and its protein levels are not completely silenced until the B cell becomes fully differentiated into a plasma cell or a memory B cell. MYC has been described as a proto-oncogene that is closely involved in many cancers, including leukemia and lymphoma. Aberrant expression of MYC protein in these hematological malignancies results in an uncontrolled rate of proliferation and, thereby, a blockade of the differentiation process. MYC is not activated by mutations in the coding sequence, and, as reviewed here, its overexpression in leukemia and lymphoma is mainly caused by gene amplification, chromosomal translocations, and aberrant regulation of its transcription. This review provides a thorough overview of the role of MYC in the developmental steps of B cells, and of how it performs its essential function in an oncogenic context, highlighting the importance of appropriate MYC regulation circuitry.
Related Concept Videos
Abnormal Proliferation
B Cell Activation and Differentiation
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
Differentiation of Common Myeloid Progenitor Cells
Induced Pluripotent Stem Cells
Somatic...
Mitogens and the Cell Cycle
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

