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Updated: Nov 23, 2025

Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
MYC dysfunction modulates stemness and tumorigenesis in breast cancer
Yiqiu Liu1, Chengjun Zhu1, Lin Tang2
1Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, China.
The MYC oncogene plays a key role in breast cancer development and progression. Its amplification predicts diagnosis and prognosis, and it interacts with cancer stem cells, influencing metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MYC is a proto-oncogene and transcription factor implicated in various cancers.
- MYC deregulation is observed in breast cancer, but its precise role and mechanisms remain unclear.
- Understanding MYC's function is crucial for breast cancer research.
Purpose of the Study:
- To investigate the role and mechanism of MYC deregulation in breast cancer.
- To analyze MYC's mRNA expression, prognostic value, and pathway interactions.
- To explore the relationship between MYC and cancer stem cells in breast cancer.
Main Methods:
- Utilized multiple public databases: UALCAN, bc-GenExMiner, TCGA, cBioportal, STRING, and Kaplan-Meier Plotter.
- Analyzed MYC mRNA expression across breast cancer subtypes.
- Examined MYC's association with signaling pathways and cancer stem cell markers.
Main Results:
- MYC expression varies across breast cancer subtypes, notably high in triple-negative breast cancer (TNBC).
- MYC influences signaling pathways (estrogen, WNT, NOTCH) and interacts with cancer stem cells.
- MYC shows significant positive correlation with stem cell markers (CD44, CD24, ALDH1).
Conclusions:
- MYC amplification serves as a potential diagnostic and prognostic biomarker in breast cancer.
- MYC's interaction with cancer stem cells is critical for breast cancer initiation and metastasis.
- MYC is a significant regulatory factor in breast cancer occurrence.
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