Related Experiment Video
Updated: Apr 27, 2026

Stimulation of Notch Signaling in Mouse Osteoclast Precursors
Published on: February 28, 2017
CD24 regulates stemness and the epithelial to mesenchymal transition through modulation of Notch1 mRNA stability by
Juyeon Lim1, Kyung-min Lee1, Jaekyung Shim2
1Department of Life Science, Hanyang University, Seoul 133-791, Republic of Korea.
Abstract:
We report here that CD24 knockdown resulted in decreased expression of Notch1 in MCF-7 cells. CD24-downstream p38MAPK was shown to regulate Notch1 at the level of mRNA stability. We also found that CD24-mediated cell migration, invasion, mammosphere formation, and drug resistance was regulated by its downstream target Notch1. Together, our results indicate that CD24 may regulate the epithelial to mesenchymal transition and stemness through Notch1 signaling in breast cancer cells.
Insights
CD24 knockdown reduces Notch1 expression in breast cancer cells. This pathway regulates cell migration, invasion, and stemness, suggesting CD24 influences epithelial-mesenchymal transition via Notch1 signaling.
Area of Science:
- Molecular Biology
- Cancer Research
- Cell Biology
Background:
- CD24 is implicated in various cancers, but its precise role in breast cancer progression remains under investigation.
- Notch1 signaling is crucial for cell fate determination and has been linked to epithelial-mesenchymal transition (EMT) and cancer stemness.
Purpose of the Study:
- To elucidate the regulatory relationship between CD24 and Notch1 signaling in breast cancer.
- To investigate the role of the CD24-Notch1 axis in mediating key cancer cell behaviors such as migration, invasion, and drug resistance.
Main Methods:
- Utilized CD24 knockdown in MCF-7 breast cancer cells.
- Assessed Notch1 expression levels and mRNA stability.
- Evaluated the impact of CD24 and Notch1 on cell migration, invasion, mammosphere formation, and drug resistance.
Main Results:
- CD24 knockdown led to decreased Notch1 expression in MCF-7 cells.
- The p38MAPK pathway was identified as a regulator of Notch1 mRNA stability downstream of CD24.
- CD24-mediated cell migration, invasion, mammosphere formation, and drug resistance were found to be regulated by Notch1.
Conclusions:
- CD24 plays a significant role in breast cancer progression.
- The CD24-Notch1 signaling pathway is a key regulator of epithelial-mesenchymal transition and stemness in breast cancer cells.
- Targeting the CD24-Notch1 axis may offer therapeutic strategies for breast cancer treatment.
More Related Videos
08:01Oct4GiP Reporter Assay to Study Genes that Regulate Mouse Embryonic Stem Cell Maintenance and Self-renewal
Published on: May 30, 2012
11:32Identification of Transcription Factor Regulators using Medium-Throughput Screening of Arrayed Libraries and a Dual-Luciferase-Based Reporter
Published on: March 27, 2020
Related Concept Videos
Role Of Notch Signalling In Intestinal Stem Cell Renewal
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Notch Signaling Pathway
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
Notch Signaling Pathway
Negative Regulator Molecules
Stem Cell Niche
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...