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The Structure and Function of DNA G-Quadruplexes
Open accessAbstract
Guanine-rich DNA sequences can fold into four-stranded, noncanonical secondary structures called G-quadruplexes (G4s). G4s were initially considered a structural curiosity, but recent evidence suggests their involvement in key genome functions such as transcription, replication, genome stability, and epigenetic regulation, together with numerous connections to cancer biology. Collectively, these advances have stimulated research probing G4 mechanisms and consequent opportunities for therapeutic intervention. Here, we provide a perspective on the structure and function of G4s with an emphasis on key molecules and methodological advances that enable the study of G4 structures in human cells. We also critically examine recent mechanistic insights into G4 biology and protein interaction partners and highlight opportunities for drug discovery.
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“Lastly, more serious DNA damages, such as double-strand breaks associated with non-B DNA structures like G4s, and the subsequent DNA repair can be mutagenic (7,27).”
From G-quadruplex-mediated genomic instability drives SNVs in cancer (2024) · cites this paper as [7]
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1 retracted
Zhang, S., Sun, H., Wang, L., Liu, Y., Chen, H., Li, Q., Guan, A., Liu, M., & Tang, Y. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky665 · Cited by 158
RetractedHallmarks of Cancer: The Next Generation
Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590 · cited 2×
“achieve unlimited proliferation by protecting ends of chromosomes [23].”
BackgroundMolecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid
WATSON, J. D., & CRICK, F. H. C. (1953) · Nature · doi:10.1038/171737a0 · Cited by 13,584 · cited 1×
“The most widely recognised DNA structure is that of the classical DNA double helix [1], which defines a structural basis for the genetic code via defined base-pairing.”
BackgroundQuadruplex DNA: sequence, topology and structure
Burge, S., Parkinson, G. N., Hazel, P., Todd, A. K., & Neidle, S. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl655 · Cited by 2,404 · cited 1×
“ogies arising from different combinations of strand direction (Figure 1D–F), as well as length and loop composition [9,10].”
BackgroundSiddiqui-Jain, A., Grand, C. L., Bearss, D. J., & Hurley, L. H. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182256799 · Cited by 2,274 · cited 9×
“A cocrystal structure of bos taurus DHX36 helicase bound to the MYC promoter G4 revealed a mode of binding in which the G4 makes contacts with a DHX36-specificmotif (DSM) and the C terminal OB-fold domain (Figure 4) [73].”
BackgroundInfluentialQuantitative visualization of DNA G-quadruplex structures in human cells
Biffi, G., Tannahill, D., McCafferty, J., & Balasubramanian, S. (2013) · Nature Chemistry · doi:10.1038/nchem.1548 · Cited by 2,173 · cited 3×
“structures in human cell lines upon ligand treatment together with depletion of the G4 resolving helicase FANCJ [41,42], to reveal increased numbers of G4 foci staining in nuclei after pyridostatin [41] or telomestatin ligand treatment and FANCJ depletion in chicken DT40 cells [42].”
BackgroundSelf-citationSen, D., & Gilbert, W. (1988) · Nature · doi:10.1038/334364a0 · Cited by 1,866 · cited 1×
“The finding that G4-rich telomeric repeats form G4 structures [6] suggested a mechanistic link with telomerase-mediated extension of telomeres, prompting an exploration of G4 stabilising ligands that may inhibit the growth of cancer cells by interfering with telomere maintenance (reviewed in [89]).”
BackgroundCrystal structure of parallel quadruplexes from human telomeric DNA
Parkinson, G., Lee, M. P. H., & Neidle, S. (2002) · Nature · doi:10.1038/nature755 · Cited by 1,863 · cited 1×
“Structural studies using X-ray crystallography and NMR spectroscopy have provided detailed insights into the structure of DNA G4s primarily based on the human telomeric repeat (Figure 1B,C) [11] or sequences derived from the promoter regions of certain human genes such as MYC or KIT [12,13].”
BackgroundPrevalence of quadruplexes in the human genome
Huppert, J. L., & Balasubramanian, S. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki609 · Cited by 1,795 · cited 2×
“Based on biophysical studies on different G4 structures, algorithms using sequence motifs such as GR3NxGR3NxGR3NxGR3 were developed and deployed to predict putative G4 structures in genomic DNA [14,15].”
BackgroundMethodSelf-citationHelix formation by guanylic acid.
Gellert, M., Lipsett, M., & Davies, D. R. (1962) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.48.12.2013 · Cited by 1,430
Flagged first, then by citations
4 of the 121 references couldn’t be matched to a known paper.
Research works printed but not linked: 4
- Bang, 1910, Untersuchungen über die Guanylsäure, Biochem. Z., 26, 293
- Testorelli, 2003, Telomerase and cancer, J. Exp. Clin. Cancer Res., 22, 165
- Anders, 2014, Genome-wide localization of small molecules, Nat. Biotechnol., 32, 92, 10.1038/nbt.2776 · DOI
- Pagano, 2015, Identification of novel interactors of human telomeric G-quadruplex DNA, Chem. Commun., 51, 2964, 10.1039/C4CC07231F · DOI
Cited by
Sorted by citations
Items 401–500 of 706
Spectroscopic Characterization of Mitochondrial G-Quadruplexes
Illodo, S., Pérez-González, C., Barcia, R., Rodríguez-Prieto, F., Al-Soufi, W., & Novo, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020925 · Cited by 5
Alkaloid Escholidine and Its Interaction with DNA Structures
Jarošová, P., Hannig, P., Kolková, K., Mazzini, S., Táborská, E., Gargallo, R., Borgonovo, G., Artali, R., & Táborský, P. (2021) · Biology · doi:10.3390/biology10121225 · Cited by 5
“G-quadruplexes are formed by guanine-rich sequences and stabilized by cations, such as K+ or Na+ [20].”
BackgroundLiu, Y., Yang, D., & Sheu, S. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.09.057 · Cited by 5
Ali, S., Lombardi, E. P., Ghosh, D., Jia, T., Vitry, G., Saker, L., Poupon, J., Teulade‐Fichou, M., Nicolas, A. G., Londoño‐Vallejo, A., et al. (2021) · Metallomics · doi:10.1093/mtomcs/mfab029 · Cited by 7
Tokan, V., Lorenzo, J. L. L., Jedlička, P., Kejnovská, I., Hobza, R., & Kejnovský, E. (2021) · Biology · doi:10.3390/biology10040347 · Cited by 5
Quadruplex DNA-guided ligand selection from dynamic combinatorial libraries of acylhydrazones.
Reznichenko, O., Cucchiarini, A., Gabélica, V., & Granzhan, A. (2020) · Organic and biomolecular chemistry · doi:10.1039/d0ob01908a · Cited by 5
Structure of a DNA G-Quadruplex Related to Osteoporosis with a G-A Bulge Forming a Pseudo-loop
Živković, M. L., Rozman, J., & Plavec, J. (2020) · Molecules · doi:10.3390/molecules25204867 · Cited by 6
Imperatore, C., Varriale, A., Rivieccio, E., Pennacchio, A., Staiano, M., d'Auria, S., Casertano, M., Altucci, C., Valadan, M., Singh, M., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197103 · Cited by 5
“Their involvement in important biological functions, such as telomere maintenance [1–3], DNA-protein recognition [4,5] and protein inhibition [6,7] has been supposed.”
Devaux, A., Bonnat, L., Lavergne, T., & Defrancq, E. (2020) · Organic and biomolecular chemistry · doi:10.1039/d0ob01311k · Cited by 5
Structure-Guided Strategies for Aptamer Screening and Optimization: Advances and Perspectives
Zhao, L., Wang, P., Qu, T., Ji, Q.-L., Zhao, X.-M., Zhao, Y.-S., & Chen, Y. (2026) · Trends in Analytical Chemistry (TrAC) · doi:10.1016/j.trac.2026.118870 · Cited by 4
Wang, Z., He, X., Zhang, X., Spiegel, J., Flynn, S. M., & Balasubramanian, S. (2026) · Nature Chemistry · doi:10.1038/s41557-026-02111-y · Cited by 6
“For example, TOP1 showed the most frequent degradation across multiple G4L-PROTACs ( 3 , 5 , 6 , 7 and 9 ), while SMARCA4 exhibited the largest fold change in degradation, particularly with G4L-PROTACs 6 , 10 and 11 .”
Self-citationLu, Z.-R., Chen, Q.-M., Hu, Y.-L., Tang, T.-T., Hayat, M., Liu, P., & Liu, Z.-M. (2026) · Microchemical journal (Print) · doi:10.1016/j.microc.2026.116944 · Cited by 4
Mock, P. Y., Chua, E., Stevens, A., Salim, F., & Lam, K. (2025) · Bioorganic chemistry (Print) · doi:10.1016/j.bioorg.2025.109150 · Cited by 4
Cabrero-Martín, A., Montiel, V. R.-V., Torrente-Rodríguez, R. M., Povedano, E., Velázquez-Gutiérrez, J., Garranzo-Asensio, M., Pingarrón, J., Barderas, R., & Campuzano, S. (2025) · Analytical Chemistry · doi:10.1021/acs.analchem.5c02715 · Cited by 4
Unwinding process of DNA/RNA quadruplexes by proteins under label-free nanopore monitoring
Ren, M.-L., Weng, T., Liang, L.-Y., Chen, X., Liu, D., Fang, S.-X., Tian, R., Xie, W.-Y., Wang, L., Wang, D., et al. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf547 · Cited by 4
“Evidence indicates that inappropriate formation of G4s may act as “knots” within genome, which are linked to human diseases and could be unfolded enzymatically [ 5–7 ].”
Decoding information stored in DNAs through single-molecule electrical detection platforms
Cheng, L., Cai, H., Zhan, Q., Jiang, Y., Li, M.-L., Jia, C.-C., & Guo, X.-F. (2025) · Innovation (Cambridge (Mass.)) · doi:10.1016/j.xinn.2025.101000 · Cited by 4
“89 G quadruplexes are rich in tandem repeat guanines 90 and hairpin structures.”
Unveiling the biological effects of DNA G-quadruplex ligands through multi-omics data integration
Romano, F., Persico, C., Barra, A., Pinto, G., Illiano, A., Amoresano, A., Aiello, I., Abate, S., D’Auria, L., Martello, V., et al. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.144325 · Cited by 8
Hile, S. E., Weissensteiner, M. H., Pytko, K. G., Dahl, J. M., Kejnovský, E., Kejnovská, I., Hedglin, M., Georgakopoulos‐Soares, I., Makova, K. D., & Eckert, K. A. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf352 · Cited by 4
“G4 structural topology is variable, with the polarity of the four strands and conformation of the interrupting loops determining whether the G4 forms a parallel, antipar-allel, or hybrid topology [ 9 , 10 ].”
Conformational Propensities of a DNA Hairpin with a Stem Sequence from the c-MYC Promoter
Garabet, A., Prislan, I., Ulrih, N. P., Wells, J. W., & Chalikian, T. (2025) · Biomolecules · doi:10.3390/biom15040483 · Cited by 4
“The ability to regulate genomic events for therapeutic advantage requires an understanding of the conformational properties of non-canonical DNA.”
Obi, I., Sengupta, P., & Sabouri, N. (2025) · bioRxiv · doi:10.1093/nar/gkaf853 · Cited by 4
“G-quadruplexes (G4s) are stable non-canonical secondary DNA and RNA structures, formed by tandem guanine (G) repeats when nucleic acids are in their single-stranded state [ 1 ].”
Štefan, U., Brázda, V., Plavec, J., & Marušič, M. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136008 · Cited by 5
Suprun, E. V., Khmeleva, S. A., Ptitsyn, K. G., Kurbatov, L., & Radko, S. (2024) · Journal of Analytical Chemistry · doi:10.1134/s1061934824700217 · Cited by 4
Zhuk, A., Stepchenkova, E., Zotova, I., Belopolskaya, O., Pavlov, Y., Kostroma, I., Gritsaev, S., & Aksenova, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105269 · Cited by 4
“G-quadruplexes are naturally formed in genomic DNA, where they play a role in processes such as gene expression regulation, chromosome organization, and chromosome end protection [6].”
BackgroundSulfur incorporation into nucleic acids accelerates enzymatic activity
Shin, H.-S., Cho, J.-Y., Park, B. Y., & Jung, C. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.152548 · Cited by 4
Prediction and validation of circulating G-quadruplexes as a novel biomarker in colorectal cancer
Zhang, H., Zhou, J., & Ye, Y. (2024) · Journal of Gastrointestinal Oncology · doi:10.21037/jgo-24-26 · Cited by 4
“Recent evidence suggests that G4 is involved in key genome functions, such as transcription, replication, genome stability, and epigenetic regulation, and has numerous connections to cancer biology, extending G4 beyond the DNA double helix (2).”
Kumari, A., Pandav, K., Panwar, A., Nath, M., Peddinti, R. K., & Barthwal, R. (2024) · Results in Chemistry · doi:10.1016/j.rechem.2024.101324 · Cited by 3
H, H., & Mallajosyula, S. (2023) · ACS Applied Materials and Interfaces · doi:10.1021/acsami.3c12262 · Cited by 4
QUFIND: tool for comparative prediction and mining of G4 quadruplexes overlapping with CpG islands
Kaur, B., Sharma, P., Arora, P., & Sood, V. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1265808 · Cited by 4
Heat capacity changes associated with G-quadruplex unfolding.
Garabet, A., Liu, L., & Chalikian, T. (2023) · Journal of Chemical Physics · doi:10.1063/5.0157749 · Cited by 4
Sabatucci, A., Girella, A., Bartolomeo, M. D., Pucci, M., Vismara, M. E. M., Benatti, B., Blacksell, I. A., Cooper, D., Dainese, E., D’Acquisto, F., et al. (2023) · Advances in Biological Regulation · doi:10.1016/j.jbior.2023.100976 · Cited by 5
Genomic distribution and polymorphism of G-quadruplex motifs occupying ovine promoters and enhancers
Stefos, G., Theodorou, G., & Politis, I. (2023) · Mammalian Genome · doi:10.1007/s00335-023-09988-x · Cited by 4
G4-interacting proteins endangering genomic stability at G4 DNA-forming sites
Kim, N. (2023) · Biochemical Society Transactions · doi:10.1042/bst20221018 · Cited by 7
Pavlova, I., Barinov, N. A., Новиков, Р. А., Severov, V. V., Iudin, M. S., Vedekhina, T., Larin, A. K., Babenko, V. V., Aralov, A. V., Gnuchikh, E. Y., et al. (2022) · Biochimie · doi:10.1016/j.biochi.2022.08.016 · Cited by 6
Monteiro, A. R., Ramos, C., Lourenço, L. M. O., Fateixa, S., Rodrigues, J., Neves, M. G., & Trindade, T. (2022) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2022.07.075 · Cited by 4
Camarillo, R., Jimeno, S., & Huertas, P. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.742434 · Cited by 5
“Thus, G4 structures can be intramolecular (formed within one strand) or intermolecular (formed frommultiple strands), parallel or antiparallel (Figure 1B) (Spiegel et al., 2020).”
BackgroundMolecular Packing Interaction in DNA Crystals
Shamim, A., Parveen, N., Subramani, V. K., & Kim, K. (2020) · doi:10.3390/cryst10121093 · Cited by 4
G-quadruplex-proximity protein labeling based on peroxidase activity
Masuzawa, T., Sato, S., Niwa, T., Taguchi, H., Nakamura, H., & Oyoshi, T. (2020) · Chemical Communications · doi:10.1039/d0cc02571b · Cited by 13
Pheophorbide–phenazinium conjugate as a fluorescent light-up probe for G-quadruplex structure
Ryazanova, O., Zozulya, V., Voloshin, I., Dubey, L., Ilchenko, M., Dubey, I., & Karachevtsev, V. (2020) · doi:10.1016/j.molstruc.2020.128218 · Cited by 4
Cao, Y.-W., Li, W., Ding, P., & Pei, R. (2020) · Chemical Communications · doi:10.1039/d0cc03082a · Cited by 4
Rajczak, E., & Juskowiak, B. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.11.163 · Cited by 4
Cabrero-Martín, A., Montiel, V. R.-V., Velázquez-Gutiérrez, J., Montero-Calle, A., Garranzo-Asensio, M., Reviejo, A. J., Pingarrón, J., Barderas, R., & Campuzano, S. (2026) · Angewandte Chemie · doi:10.1002/anie.3768019 · Cited by 3
Domínguez, A., Navarro, N., Aviñó, A. M., Fàbrega, C., & Eritja, R. (2026) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2026.2659926 · Cited by 4
“G4s are four-stranded, non-canonical nucleic acid structures formed in guanine-rich sequences through the stacking of two or more G-tetrads or G-quartets [16,17].”
InfluentialShin, H., Yoon, J., Kim, Y., & Jung, C. (2026) · ACS Sensors · doi:10.1021/acssensors.5c04395 · Cited by 3
Sokulska, M., Nalewaj, M., Czapik, T., Rachwalak, M., & Szabat, M. (2026) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2026.102906 · Cited by 6
“151,152 Targeting G4 structures with ASO is often further complicated by competition with endogenous RNA-binding proteins (RBPs) that recognize and bind G-quadruplexes in cells.”
High-Sensitivity DNA Aptasensors for Detecting Salivary Biomarker S100A7 in Heart Failure
Schwenke, T., Sequeira, M., Mutschler, R., Punyadeera, C., Beliaev, A., Alexandrov, K., & Eremeeva, E. (2026) · ACS Omega · doi:10.1021/acsomega.5c11711 · Cited by 3
Functional nucleic acids empower CRISPR/Cas: A novel dimension in label-free rapid detection
Yu, Z., Shi, C., Tan, H., Li, W., Wang, Y., Zhang, Q., Xiao, P., & Man, Y. (2026) · Trends in Analytical Chemistry (TrAC) · doi:10.1016/j.trac.2025.118512 · Cited by 3
Bao, Y., Wu, S.-C., Guo, L., Song, X., Ren, Z., Zhao, J., Wang, M., Chen, L., Cheng, B., Hou, X., et al. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202523769 · Cited by 5
Raevens, S., Danino, Y. M., Desingle, C., Sperti, F. R., Pirrotta, M., Mazzucotelli, L., Letissier, L., Hornstein, E., Cianférani, S., Hernandez‐Alba, O., et al. (2025) · ACS Bio & Med Chem Au · doi:10.1021/acsbiomedchemau.5c00162 · Cited by 3
Li, X., Cevec, M., Dubins, D., Plavec, J., & Chalikian, T. (2025) · Chemistry · doi:10.1002/chem.202502670 · Cited by 3
Arciuolo, V., D’Aria, F., Caruso, M. R., Calvino, M. M., Amato, J., Lazzara, G., Milioto, S., Giancola, C., Cavallaro, G. P., & Pagano, B. (2025) · The Chemical Record · doi:10.1002/tcr.202500126 · Cited by 2
Advances of HDAC dual inhibitors in breast cancer treatment.
Wu, C.-J., Wu, J.-Y., Ni, L., Liang, M., Feng, R., Kong, X., Zhou, H.-L., & Nie, J. (2025) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2025.118372 · Cited by 3
Mosley, S. R., Lapa, N., Namdar, A., Catley, T. E., Meier-Stephenson, F., Mowat, C., Gao, P., Sun, X., Meier-Stephenson, V., Pyne, A. L. B., et al. (2025) · bioRxiv · doi:10.1101/2025.07.17.665440 · Cited by 3
“Here, we investigate the role of cyDNA structures in MSI and CIN cyDNA, particularly in terms of G-quadruplexes (G4s), a DNA structure formed by guanine repeats common within promoter regions that influence gene transcription 29 .”
InfluentialPlatella, C., Ciolo, S. D., Criscuolo, A., Malpicci, D., Gaglione, R., Arciello, A., Musumeci, D., Lucenti, E., Cariati, E., Montesarchio, D., et al. (2025) · Archiv der Pharmazie · doi:10.1002/ardp.70037 · Cited by 3
Bisoi, A., & Singh, P. C. (2025) · Biointerphases · doi:10.1116/6.0004389 · Cited by 3
Chantzi, N., Liew, S. W., Wijaya, A., Chan, C. S. Y., Mouratidis, I., Amaral, E. D. O. S., Uzun, Y., Hemberg, M., Vasquez, K. M., Kwok, C.-K., et al. (2025) · bioRxiv · doi:10.1101/2025.06.17.660256 · Cited by 3
“G4s are formed via Hoogsteen hydrogen bonding, which links four guanine bases into a square planar structure known as a G-quartet, which are then stacked on top of each other to form G4 DNA structures (1).”
Tsvetkov, V. B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26135979 · Cited by 3
Soriano‐Lerma, A., Sánchez-Martín, V., Murciano‐Calles, J., Ortiz-González, M., Tello-Lopez, M. J., Pérez‐Carrasco, V., Linde-Rodríguez, Á., Ramírez-Macías, I., Gómez‐Pinto, I., López‐Aliaga, I., et al. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00747-1 · Cited by 2
“RSV’s polyphenolic structure along with its aromatic surface, appropriate for π–π stacking with G-tetrads [21], suggest that RSV may also display G4 binding properties.”
Wang, X., Yang, H., Geng, X., Zhao, X., Zhu, L.-J., & Xu, W.-T. (2025) · Talanta: The International Journal of Pure and Applied Analytical Chemistry · doi:10.1016/j.talanta.2025.127950 · Cited by 3
Flipons enable genomes to learn by intermediating the exchange of energy for information
Herbert, A. G. (2025) · Journal of The Royal Society Interface · doi:10.1098/rsif.2025.0049 · Cited by 4
“The literature for Z-DNA, G-quadruplex es, triplexes, and more recently, for i-motifs is quite extensive with the cellular biology of Z-DNA and G-quadruplexes best understood [45,82–84].”
A novel L-RNA aptamer to regulate the pUG fold RNA-induced gene expression in vivo
Liew, S. W., Cao, D., Petersen, R. J., Butcher, S. E., Kennedy, S. G., & Kwok, C.-K. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf137 · Cited by 3
“These structures consist of stacked G-quartets, which are planar arrangements of four G bases held together by Hoogsteen hydrogen bonds [ 2 , 3 ].”
Yang, M. J., Lee, H., Kang, D., & Park, C. (2025) · FEBS Journal · doi:10.1111/febs.70047 · Cited by 2
“G-quadruplexes are highly stable secondary structures formed in G-rich regions of DNA [50].”
Bisoi, A., Majumdar, T., Sarkar, S., & Singh, P. C. (2025) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.4c05133 · Cited by 4
Selective delivery of G-quadruplex ligand in glioma cell lines: the power of cyclic-RGD peptide
Pirota, V., Bisbano, G., Oldani, A., Bernardi, E., Serra, M., Paolillo, M., & Doria, F. (2024) · Scientific Reports · doi:10.1038/s41598-024-81513-9 · Cited by 3
Pérez-Soto, M., Peñalver, P., Muñoz-Báez, P., Tolosa, J., García-Martínez, J. C., Cebrián, R., & Morales, J. (2024) · Molecules · doi:10.3390/molecules29245875 · Cited by 3
“These structures have attracted significant attention due to their involvement in essential biological processes and their potential as therapeutic targets [1].”
A novel role for nonactin: interfering with G-quadruplex in RET-driven medullary thyroid cancer
Alqahtani, T., Alsubait, A., Aloumi, M., Alamer, A. K., Alomari, G., Alwassil, O., Obaidullah, A., & Alghamdi, S. (2024) · BMC Cancer · doi:10.1186/s12885-024-13345-9 · Cited by 3
“This promoter lacks the GC box region, rendering it incapable of forming the G-quadruplex structure [27].”
Dissecting non-B DNA structural motifs in untranslated regions of eukaryotic genomes
Gummadi, A. S. C., Muppa, D. K., & Yella, V. R. (2024) · Genomics & Informatics · doi:10.1186/s44342-024-00028-x · Cited by 3
“Here, blue represents the organisms that have the greatest number of non-B DNA motifs in the 5 ′ UTR, and red represents the organisms that have the greatest number of non-B DNA motifs in the 3 ′ UTR [12, 21].”
Pradhan, S., Campanile, M., Sharma, S., Oliva, R., & Patra, S. (2024) · Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.4c01806 · Cited by 3
Determination of ligand selectivity to G-tetrad through an AMCA fluorescence quenching approach.
Zhong, F., Sun, R., Huang, S.-P., Guo, P.-Q., Li, Q., Wang, L., Sun, H.-X., & Yao, L. (2024) · Talanta: The International Journal of Pure and Applied Analytical Chemistry · doi:10.1016/j.talanta.2024.126732 · Cited by 3
Interaction analysis of RNA G-quadruplex with ligands and in situ imaging application.
Jiang, L.-X., Teng, J., Liu, X., Xu, L., Yang, T.-T., Hu, X.-P., Ding, S.-J., Li, J., Jiang, Y., & Cheng, W. (2024) · Analytical Biochemistry · doi:10.1016/j.ab.2024.115613 · Cited by 3
Non-B DNA in plant genomes: prediction, mapping, and emerging roles.
Ferrero, L. V., Zhang, W.-L., Benhamed, M., Crespi, M., & Ariel, F. (2024) · Trends in Plant Science · doi:10.1016/j.tplants.2024.06.011 · Cited by 3
Analysis of live cell data with G-DNABERT supports a role for G-quadruplexes in chromatin loopingPreprint
Konovalov, D., Umerenkov, D., Herbert, A. G., & Poptsova, M. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.21.599985 · Cited by 2
“Regular classic pattern detects over 370,000 G4 sequence motifs in the human genome depending on the motif searched for 14 .”
BackgroundProtein G-quadruplex interactions and their effects on phase transitions and protein aggregation
Sahoo, B. R., Kocman, V., Clark, N., Myers, N., Deng, X., Wong, E. L., Yang, H., Kotar, A., Guzmán, B. B., Dominguez, D., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae229 · Cited by 19
“They can stack over one another through π – π integration to form compact and ordered structures ( 20 ).”
Chery, M., Berrissou, C., Humbert, N., Hummel, G., Mély, Y., Salinas-Giegé, T., & Drouard, L. (2023) · The Plant Journal · doi:10.1111/tpj.16596 · Cited by 3
Kircheva, N., Petkova, V., Dobrev, S., Nikolova, V., Angelova, S., & Dudev, T. (2023) · Molecules · doi:10.3390/molecules28248130 · Cited by 3
Kircheva, N., Dobrev, S., Petkova, V., Bakalova, S. M., Kaneti, J., & Angelova, S. (2023) · Molecules · doi:10.3390/molecules28166109 · Cited by 4
“This result corresponds well to experimental data claiming the inability of the sodium cation to compete with the native potassium one in these structures [13,14,16,19,35].”
BackgroundResultExploring Artificial Nucleic Acid Mimicking Peptide Nanofibers
Hendrikse, S. I. S., Todorova, N., Soleimaninejad, H., Charchar, P., Sani, M., Taief, K. A., Berengut, J. F., Wickham, S., Gras, S., Fahrenbach, A., et al. (2023) · Chemistry of Materials · doi:10.1021/acs.chemmater.3c00445 · Cited by 3
Ulum, L. L., Karikome, Y., Yagi, R., Kawashima, T., Ishihara, A., & Oyoshi, T. (2023) · ACS Omega · doi:10.1021/acsomega.3c00050 · Cited by 3
Novotný, A., Plavec, J., & Kocman, V. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad117 · Cited by 3
Biswas, S., Basak, S., Samui, S., Pasadi, S., Muniyappa, K., & Naskar, J. (2023) · ChemistrySelect · doi:10.1002/slct.202203563 · Cited by 3
Monchaud, D. (2023) · Molecules and Cells · doi:10.1016/j.molcel.2022.12.010 · Cited by 3
Probing telomereric-like G4 structures with full or partial 2'-deoxy-5-hydroxyuridine substitutions.
Szeltner, Z., Ferenc, G., Juhász, T., Kupihar, Z., Váradi, Z., Szüts, D., & Kovács, L. (2023) · Biochimie · doi:10.1016/j.biochi.2023.01.009 · Cited by 3
Telomeres as dynamic structures of human genome: the effect of endogenous and exogenous factors
Krapivin, M. I., Sagurova, Y. M., Efimova, O. A., Tikhonov, A. V., & Pendina, A. A. (2022) · Ecological genetics · doi:10.17816/ecogen106539 · Cited by 3
“Согласно этой гипотезе, гуанины из разных повторов образуют дополнительные водородные связи друг с другом, что обеспечивает достаточно стабильную структуру [19, 20].”
Asha, H., Stadlbauer, P., Martínez‐Fernández, L., Banáš, P., Šponer, J., Improta, R., & Esposito, L. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.11.143 · Cited by 5
Wickhorst, P. J., Ihmels, H., & Paululat, T. (2021) · Molecules · doi:10.3390/molecules26216595 · Cited by 3
G-quadruplex–R-loop interactions and the mechanism of anticancer G-quadruplex binders
Miglietta, G., Russo, M., & Capranico, G. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa1206 · Cited by 3
“G4 structures are heterogenous and many distinct conformations have been reported (1,2,11,84), however their roles in the mechanism of action of G4 binders is not known.”
BackgroundTowards understanding the interaction of (S)-thalidomide with nucleobases.
Baranowska-Łączkowska, A., Banaszak-Piechowska, A., Donarska, B., & Łączkowski, K. Z. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108566 · Cited by 3
Ferenc, G., Váradi, Z., Kupihár, Z., Paragi, G., & Kovács, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144981 · Cited by 3
Oskouie, A. A., & Abiri, A. (2020) · Analytical Biochemistry · doi:10.1016/j.ab.2020.113744 · Cited by 3
Malina, J., Kostrhunová, H., Farrell, N., & Brabec, V. (2021) · doi:10.1039/d1qi00488c · Cited by 3
Photocatalytic proximity labeling for the identification of G-quadruplex DNA-interacting proteins
Abdelhady, A. M., Sato, S., Masuzawa, T., Deguchi, K., Oba, M., Sato, T., Mase, N., Yamanaka, T., Osman, J. A., Kato, M., et al. (2026) · Communications Chemistry · doi:10.1038/s42004-026-02170-9 · Cited by 3
“G-quadruplexes (G4s) are four-strandednucleic acid structures folded under physiological conditions within guanine (G)-rich regions; they comprise two or more stacked G-tetrads 20,21 .”
D'Anna, L., Contino, S., Marinello, R., Fares, J., Simone, G. D., Monari, A., Barbault, F., Barone, G., Terenzi, A., & Perricone, U. (2026) · ACS Omega · doi:10.1021/acsomega.6c03072 · Cited by 2
Luchian, T., Cimpanu, A., Park, J., Mereuta, L., & Park, Y. (2026) · Small Methods · doi:10.1002/smtd.70691 · Cited by 2
“DNA replication, gene expression, telomere maintenance, and transcription [ 33, 67 ].”
Kroft, C. W., Krall, J. B., Warchoł, M., Welty, R., Herbert, A., Henen, M., & Vögeli, B. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag419 · Cited by 2
“The charged face binds to B-DNA and the hydrophobic face to the hydrophobic end caps of the GQ in a similar manner by which small molecules have been shown to bind GQs [ 41 ].”
Wang, R., Zhou, J.-R., & Hu, M.-H. (2026) · Sensors and Actuators B: Chemical · doi:10.1016/j.snb.2026.139799 · Cited by 2
Salim, M., Paloque, L., Reyser, T., Nardella, F., Augereau, J., Luo, Y., Britton, S., Mergny, J., Gervais, V., Benoit‐Vical, F., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.07.698092 · Cited by 1
Herbert, A. G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms27010272 · Cited by 3
“The structure-specific interactions are validated using a non-GQ-forming oligonucleotide with the isoelectric substituent 7-deaza, 8-aza-guanosine bases as controls [38].”
Porzio, A. D., Pecoraro, A., Danisi, C., Persico, C., D’Auria, L., Germoglio, M., Iaccarino, N., Feliciello, I., Giancola, C., Randazzo, A., et al. (2025) · NAR Cancer · doi:10.1093/narcan/zcaf046 · Cited by 1
“…into G4 structures are predominantly located at biologically relevant nuclear genomic sites, such as telomeres and oncogene promoters [ 24 , 25 ], as well as within the mitochondrial DNA [ 26 , 27 ], suggesting that these structures could offer exciting therapeutic opportunities [ 23 , 28 ].”
AIEgen Functionalized Polymer Ring
Qu, K., Xiong, Z., Gu, A., Yang, S., Hu, B., Zhang, H., & Yang, Z. (2025) · Macromolecules · doi:10.1021/acs.macromol.5c02698 · Cited by 2
Xia, Y., Zhang, Y., Li, H., Qiu, Z., Zhao, Y., Mo, L., & Luo, X. (2025) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2025.127163 · Cited by 1
Modulating a Massive Set of Biomolecular Structures by Sono‐Mechanical Force
Pokhrel, P., Sharma, G., Jenyk, J., Lower, A., Ji, J.-H., Shakya, S., Haun, J., & Mao, H.-B. (2025) · Advancement of science · doi:10.1002/advs.202511687 · Cited by 2
Metadata
- Authors
- Spiegel, J., Adhikari, S., & Balasubramanian, S.
- Affiliations
- Cancer Research UK (GB)
- University of Cambridge (GB)
- Corresponding author
- Balasubramanian, Shankar
- Venue
- Trends in Chemistry
- Publisher
- Elsevier BV
- Published
- 2020-02
- Volume
- 2
- Issue
- 2
- Pages
- 123-136
- ISSN
- 2589-5974 (ISSN-L)
- PMC
- PMC7472594
- OpenAlex
- W2966334511
- Cited by
- 920
- References
- 121
- Citations by year
- 2026: 111 · 2025: 157 · 2024: 158 · 2023: 144 · 2022: 151 · 2021: 122 · 2020: 74
- FWCI
- 7.73
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Trends in Chemistry (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Apollo (University of Cambridge) (submittedVersion, cc-by-nc-nd)
- Apollo
- Funders
- Wellcome Trust
- Cancer Research UK
- Horizon 2020 Framework Programme
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced biosensing and bioanalysis techniques
- Health Sciences › Medicine › Oncology › Metal complexes synthesis and properties
- Keywords
- G-quadruplex, guanine-rich DNA, genome stability, transcription, DNA replication, epigenetic regulation, cancer, G-quadruplex-binding proteins
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