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Published on: September 25, 2021
Machine Learning-Based Virtual Screening for the Identification of Novel CDK-9 Inhibitors
Lisa Piazza1, Clarissa Poles2,3, Giulia Bononi1
1Department of Pharmacy, University of Pisa, 56126 Pisa, Italy.
Abstract:
Cyclin-dependent kinase 9 (CDK9) is a key regulator of transcriptional elongation and DNA repair, supporting cancer cell survival by sustaining the expression of oncogenes and anti-apoptotic proteins. Its overexpression in multiple malignancies makes it an attractive target for anticancer therapy. Here, we report a machine learning (ML) based approach to identify novel CDK9 inhibitors. Through systematic data collection and preprocessing, seventy predictive models were developed using five algorithms, two classification settings, and seven molecular representations. The best-performing model was employed to guide a virtual screening (VS) campaign, resulting in the identification of 14 compounds promising for their potential inhibitory effect. Upon enzymatic assays, two molecules with inhibitory activity in the low micromolar range were selected as promising candidates and further tested in three cancer cell lines with distinct genetic backgrounds. These experiments led to the identification of a novel compound exhibiting interesting therapeutic potential, both as a single agent and in combination with Camptothecin (CPT), revealing varying response profiles across the tested cell lines. These results illustrate the power of integrating ML within anticancer drug discovery pipelines and represent a valuable starting point for the development of novel CDK9 inhibitors.
Insights
Machine learning identified novel compounds targeting Cyclin-dependent kinase 9 (CDK9), a protein crucial for cancer cell survival. One compound shows therapeutic potential as a single agent or in combination with Camptothecin.
Area of Science:
- Oncology
- Computational Chemistry
- Drug Discovery
Background:
- Cyclin-dependent kinase 9 (CDK9) is vital for cancer cell survival, regulating oncogene and anti-apoptotic protein expression.
- CDK9 overexpression in malignancies positions it as a key therapeutic target for anticancer strategies.
Purpose of the Study:
- To develop and apply a machine learning (ML) approach for identifying novel inhibitors of CDK9.
- To validate potential CDK9 inhibitors through enzymatic assays and cancer cell line testing.
Main Methods:
- Systematic data collection and preprocessing to build seventy predictive ML models.
- Virtual screening (VS) guided by the best-performing ML model to identify candidate inhibitors.
- Enzymatic assays and subsequent testing of lead compounds in diverse cancer cell lines.
Main Results:
- Identification of 14 promising compounds from virtual screening.
- Two compounds demonstrated low micromolar inhibitory activity.
- A novel compound exhibited therapeutic potential, both alone and in combination with Camptothecin (CPT), with varying efficacy across cell lines.
Conclusions:
- Machine learning effectively integrated into drug discovery pipelines for identifying novel anticancer agents.
- The identified novel compound represents a promising starting point for developing new CDK9-targeted therapies.
- The study highlights the potential of CDK9 inhibition in cancer treatment, with combination therapy showing promise.
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