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Updated: Jul 4, 2026

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells
Published on: July 30, 2020
Aurora kinase family: a new target for anticancer drug
Teresa Macarulla1, Francisco Javier Ramos, Josep Tabernero
1Medical Oncology Department, Vall d'Hebron University Hospital, Barcelona, Spain.
Abstract:
Aurora kinases (AK) are the name given to a family of Serine/threonine (Ser/Thr) protein kinases. These proteins represent a novel family of kinases crucial for cell cycle control. The cell division process is one of the hallmarks of every living organism. Within the complete cell-cycle process, mitosis constitutes one of the most critical steps. The main purpose of mitosis is to segregate sister chromatics into two daughters cells. It is a complex biologic process, and errors in this mechanism can lead to genomic instability, a condition associated with tumorigenesis. This process is tightly regulated by several proteins, some of them acting as check-points that ultimately ensure the correct temporal and spatial coordination of this critical biologic process. Among this network of mitotic regulators, AK play a critical role in cellular division by controlling chromatid segregation. Three AK family members have been identified in mammalian cells: A, B, and C. These proteins are implicated in several vital events in mitosis. In experimental models, overexpression of AK can induce spindle defects, chromosome mis-segregation, and malignant transformation. Conversely, downregulation of AK expression cause mitotic arrest and apoptosis in tumor cell lines. The expression levels of human AK are increased in certain types of cancer including breast, colon, pancreatic, ovarian, and gastric tumors. This observation has lent an interest to this family of kinases as potential drug targets for development of new anticancer therapies. This review focuses in recent progress in the role of AK in tumorogenesis and the development of new anticancer drug against AK proteins. This manuscript also includes some relevant patents as well.
Insights
Aurora kinases (AK) are critical for cell division and mitosis. Their dysregulation is linked to cancer, making them promising targets for new anticancer therapies.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Aurora kinases (AK) are Serine/threonine protein kinases vital for cell cycle control.
- Mitosis, the process of segregating sister chromatids, is crucial for cell division, and errors can lead to genomic instability and cancer.
- AK are key regulators of chromatid segregation during mitosis.
Purpose of the Study:
- To review the role of Aurora kinases in tumorogenesis.
- To discuss the development of novel anticancer drugs targeting Aurora kinases.
- To highlight recent advancements and relevant patents in AK-targeted cancer therapy.
Main Methods:
- Literature review of studies on Aurora kinases in cell cycle regulation and cancer.
- Analysis of experimental models demonstrating the effects of AK overexpression and downregulation.
- Examination of clinical data on AK expression in various human cancers.
Main Results:
- Overexpression of AK in experimental models leads to spindle defects, chromosome mis-segregation, and malignant transformation.
- Downregulation of AK induces mitotic arrest and apoptosis in tumor cell lines.
- Elevated AK expression is observed in breast, colon, pancreatic, ovarian, and gastric tumors, indicating their oncogenic role.
Conclusions:
- Aurora kinases play a significant role in cell division and are implicated in the development of various cancers.
- The inhibition of Aurora kinases presents a promising strategy for developing new anticancer drugs.
- Targeting Aurora kinases offers a potential therapeutic avenue for cancer treatment.
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