Evidence map›Paper›PMID 40533769›Full record

ReviewMolecular cancer2025

Aurora kinases signaling in cancer: from molecular perception to targeted therapies.

Prerna Vats, Chainsee Saini, Bhavika Baweja, Sandeep K Srivastava, Ashok Kumar, Atar Singh Kushwah, Rajeev Nema

Abstract readReview
In one paragraph

Review in Molecular cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

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  19. Discovery of thieno[2,3-RSC advances · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Prerna VatsDepartment of Biosciences, Manipal University Jaipur, Dehmi Kalan, Jaipur- Ajmer Expressway, Jaipur, Rajasthan, 303007, India.
Chainsee SainiDepartment of Biosciences, Manipal University Jaipur, Dehmi Kalan, Jaipur- Ajmer Expressway, Jaipur, Rajasthan, 303007, India.
Bhavika BawejaDepartment of Biosciences, Manipal University Jaipur, Dehmi Kalan, Jaipur- Ajmer Expressway, Jaipur, Rajasthan, 303007, India.
Sandeep K SrivastavaDepartment of Biosciences, Manipal University Jaipur, Dehmi Kalan, Jaipur- Ajmer Expressway, Jaipur, Rajasthan, 303007, India.
Ashok KumarDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, Saket Nagar, Bhopal, Madhya Pradesh, 462020, India.
Atar Singh KushwahWomen's Biomedical Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Rajeev NemaDepartment of Biosciences, Manipal University Jaipur, Dehmi Kalan, Jaipur- Ajmer Expressway, Jaipur, Rajasthan, 303007, India. rajeev.nema@jaipur.manipal.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aurora kinases, AURKA, AURKB, and AURKC, are serine/threonine kinases that play a vital role in regulating cell division and mitosis, particularly in the separation of chromosomes. These kinases are often overexpressed in human tumor cell lines, indicating their potential involvement in tumorigenesis. Preliminary evidence supports the use of Aurora kinase inhibitors for certain types of tumors, several AURKs inhibitors are currently under phase I and II trials. As a result, there is a growing interest in identifying small-molecule Aurora kinase inhibitors to develop as anti-cancer agents. The regulation of the cell cycle, including mitosis, is increasingly recognized as a key target in the fight against various forms of cancer. Novel drugs are being designed to inhibit the function of regulatory proteins, such as Aurora kinases, with the goal of creating personalized treatments. This review summarizes the biology of Aurora kinases in the context of cancer, integrating both preclinical and clinical data. It discusses the challenges and opportunities associated with using Aurora kinases to enhance cancer treatment. Future directions for Aurora kinase-based therapies include developing more selective inhibitors that minimize off-target effects and improve therapeutic efficacy. Researchers are also exploring combination therapies that use Aurora kinase inhibitors alongside other targeted treatments to overcome resistance and improve patient outcomes. Additionally, advancements in biomarker discovery are expected to facilitate the identification of patients most likely to benefit from Aurora kinase-targeted therapies, paving the way for more personalized approaches to cancer treatment.

Indexed as

Aurora KinasesMolecular Targeted TherapyNeoplasmsProtein Kinase InhibitorsSignal TransductionAnimalsAntineoplastic AgentsHumansAntineoplastic AgentsAurora KinasesProtein Kinase InhibitorsAKIsAURKAAURKBAURKCCancer Diagnosis and PrognosisTargeted Therapy

Identifiers

PMID40533769
PMCPMC12175390

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.