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Updated: May 12, 2026

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells
Published on: July 30, 2020
Gene amplification and overexpression of Aurora-C in breast and prostate cancer cell lines
Ali Zekri1, Vahid Lesan, Seyed H Ghaffari
1Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
Human aurora kinases are three highly conserved serine/threonine kinases with regulatory function in chromosome alignment, chromosome segregation, and cytokinesis during cell cycle progression and their overexpression associates with malignant transformation and proliferation of cancer cells. Aurora genes are located at loci that are commonly altered in cancers. Aurora-A has oncogenic activity while Aurora-B does not. Aurora-C is only detected in mammals with involvement in meiosis. Oncogenic activity of Aurora-C is still in dispute. We evaluated the expression of three Aurora kinases by real-time RT-PCR in well-known breast and prostate cancer cell lines. Cell cycle was studied with flow cytometry. In both more invasive cell lines' p53-null cells, PC-3 and MDA-MB-231, an increase in mRNA expression of three Aurora kinases, especially Aurora-C, was observed. Genomic DNA was examined for gene amplification and aneuploidy as a mechanism of overexpression. At DNA level, only Aurora-C showed gene amplification in breast cancer cell lines (p < 0.005). Here we provide evidence for the first time of Aurora-C overexpression and gene amplification.
Insights
Aurora kinases regulate cell division and are linked to cancer. This study found Aurora-C overexpression and gene amplification in breast and prostate cancer cells, suggesting its oncogenic role.
Area of Science:
- Molecular Biology
- Cell Biology
- Oncology
Background:
- Aurora kinases are crucial for cell cycle regulation.
- Their overexpression is linked to cancer development and proliferation.
- The specific role of Aurora-C in cancer remains debated.
Purpose of the Study:
- To investigate the expression of Aurora kinases (A, B, and C) in breast and prostate cancer cell lines.
- To explore the mechanisms of overexpression, including gene amplification and aneuploidy.
- To provide evidence for the oncogenic activity of Aurora-C.
Main Methods:
- Real-time RT-PCR was used to evaluate Aurora kinase mRNA expression.
- Flow cytometry was employed to study cell cycle progression.
- Genomic DNA analysis was performed to detect gene amplification and aneuploidy.
Main Results:
- Increased mRNA expression of all three Aurora kinases was observed in invasive, p53-null cancer cell lines (PC-3, MDA-MB-231).
- Aurora-C showed particularly notable overexpression.
- Gene amplification of Aurora-C was identified in breast cancer cell lines (p < 0.005).
Conclusions:
- This study provides the first evidence of Aurora-C overexpression and gene amplification in cancer cells.
- These findings support a potential oncogenic role for Aurora-C in breast and prostate cancers.
- Further research into Aurora-C's specific mechanisms in tumorigenesis is warranted.
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