Unveiling the biological effects of DNA G-quadruplex ligands through multi-omics data integration

G-quadruplexes (G4s) are non-canonical DNA structures that have proved to play a pivotal role in various biological processes, including telomere maintenance and gene expression regulation. Owing to their prevalence in tumor cells, G4s have emerged as promising targets for cancer therapy, with a substantial body of research demonstrating the potential of G4 ligands as anti-cancer tools. Nonetheless, a comprehensive multi-omics study to fully elucidate the mode of action of G-quadruplex ligands is still lacking. Such an investigation would be crucial for advancing the development of potent G4-based therapies against cancer. Herein, we employed a multi-omics approach, integrating transcriptomics, proteomics, and metabolomics, to identify key signaling pathways that mediate the anti-cancer effects of well-characterized G4-binding agents (berberine, pyridostatin and RHPS4) on human cervical adenocarcinoma (HeLa) cells. Particularly, we analyzed gene expression changes using RNA sequencing, quantified proteins by liquid-chromatography tandem mass spectrometry and examined metabolite levels via nuclear magnetic resonance. Our results revealed that, under the investigated experimental conditions, berberine treatment had only negligible cellular effects. In contrast, pyridostatin induced significant changes at the transcriptomic, proteomic, and metabolomic levels, decreasing the abundance of enzymes involved in cellular energy production, reducing the availability of precursors for lipid and nucleotide biosynthesis, and depleting essential cofactors and enzymes required for redox balance. Notably, RHPS4 could selectively disrupt mitochondrial activity, possibly through the specific stabilization of mitochondrial G-quadruplex structures. Overall, our findings provide a valuable multi-omics perspective on the cellular changes driven by G-quadruplex binders, that may accelerate the development of effective anti-cancer G4-targeted therapies.

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Publication Details

Journal
International Journal of Biological Macromolecules
Published
2025-05-16
DOI
https://doi.org/10.1016/j.ijbiomac.2025.144325
Citations
4
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
3.22

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article

Unveiling the biological effects of DNA G-quadruplex ligands through multi-omics data integration

Gabriella Pinto, Simona Marzano, Federica D’Aria, Rosario Ammendola et al.
4 citations
International Journal of Biological Macromolecules
DNA and Nucleic Acid Chemistry
3.22
article

Unveiling the biological effects of DNA G-quadruplex ligands through multi-omics data integration

Gabriella Pinto, Simona Marzano, Federica D’Aria, Rosario Ammendola, Anna Di Porzio, Nunzia Iaccarino, Diego Brancaccio, Luana Izzo, Rasmus Bro, Angela Amoresano, Nunzio D’Agostino, Morten Arendt Rasmussen, Ludovica D’Auria, Anna Illiano, Mariateresa Giustiniano, Camilla Russo, Francesco Merlino, S Abate, Fabio Cattaneo, Stefano Amente, Antonio Randazzo, Bruno Pagano, I. Aiello, Stefano De Tito, Jussara Amato, Ayslan Barra, Francesca Romano, Myrhiam Cassese, Carolina Persico, Verdiana Martello
article en
4 citations

Abstract

G-quadruplexes (G4s) are non-canonical DNA structures that have proved to play a pivotal role in various biological processes, including telomere maintenance and gene expression regulation. Owing to their prevalence in tumor cells, G4s have emerged as promising targets for cancer therapy, with a substantial body of research demonstrating the potential of G4 ligands as anti-cancer tools. Nonetheless, a comprehensive multi-omics study to fully elucidate the mode of action of G-quadruplex ligands is still lacking. Such an investigation would be crucial for advancing the development of potent G4-based therapies against cancer. Herein, we employed a multi-omics approach, integrating transcriptomics, proteomics, and metabolomics, to identify key signaling pathways that mediate the anti-cancer effects of well-characterized G4-binding agents (berberine, pyridostatin and RHPS4) on human cervical adenocarcinoma (HeLa) cells. Particularly, we analyzed gene expression changes using RNA sequencing, quantified proteins by liquid-chromatography tandem mass spectrometry and examined metabolite levels via nuclear magnetic resonance. Our results revealed that, under the investigated experimental conditions, berberine treatment had only negligible cellular effects. In contrast, pyridostatin induced significant changes at the transcriptomic, proteomic, and metabolomic levels, decreasing the abundance of enzymes involved in cellular energy production, reducing the availability of precursors for lipid and nucleotide biosynthesis, and depleting essential cofactors and enzymes required for redox balance. Notably, RHPS4 could selectively disrupt mitochondrial activity, possibly through the specific stabilization of mitochondrial G-quadruplex structures. Overall, our findings provide a valuable multi-omics perspective on the cellular changes driven by G-quadruplex binders, that may accelerate the development of effective anti-cancer G4-targeted therapies.

International Journal of Biological MacromoleculesVol. 313
University of Copenhagen (DK), University of Naples Federico II (IT)
Associazione Italiana per la Ricerca sul Cancro
Openalex Percentile: Top 8%
DNA and Nucleic Acid Chemistry
3.22
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