-
Something wrong with this record ?
Illuminating the dark: PEGylated carboxylated graphene quantum dots and curcumin in nucleolar activity and PDT-induced DNA damage in cancer
H. Dilenko, K. Bartoň Tománková, E. Hinde, L. Válková, M. Kolaříková, H. Kolářová
Language English Country France
Document type Journal Article
- MeSH
- Cell Nucleolus * drug effects metabolism MeSH
- DNA Breaks, Double-Stranded drug effects MeSH
- Photochemotherapy * methods MeSH
- Photosensitizing Agents * pharmacology MeSH
- Graphite * chemistry pharmacology MeSH
- Curcumin * pharmacology chemistry MeSH
- Quantum Dots * chemistry MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- Neoplasms * drug therapy MeSH
- Polyethylene Glycols * chemistry pharmacology MeSH
- DNA Damage * drug effects MeSH
- Reactive Oxygen Species metabolism MeSH
- Cell Survival drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Many photosensitive substances suitable for photodynamic therapy (PDT) have limited applications due to their insufficient solubility in polar solvents. Our research overcomes this challenge by means of nanotechnology in order to transform hydrophobic compounds into stable aqueous solutions, enabling them to use their full potential and unique properties in cancer therapy. In this study, the novel nano-composite cGQDs-PEG-curcumin was developed to overcome the insolubility of curcumin in water and its extraordinary efficacy in PDT was evaluated. Complex characterization was performed using high-resolution transmission electron microscopy (HR-TEM), FTIR, and UV-Vis spectroscopy. Further analysis involved fluorescence lifetime imaging (FLIM), and its cellular localization was mapped with confocal microscopy. In order to evaluate PDT effectiveness, cells treated with cGQDs-PEG-curcumin were irradiated with 5 J/cm2 of 414 nm light. After irradiation, cell viability assay, scanning electron microscopy (SEM), reactive oxygen species (ROS) detection, comet assay, and γH2AX-based DNA double-strand breaks (DSBs) detection were assessed and revealed a remarkable ability of the nano-composite to induce DNA damage after irradiation without ROS production. Our findings highlight the potential of cGQDs-PEG-curcumin as a cutting-edge PDT agent, capable of disrupting cell membrane and nucleolar integrity and impairing ribosomal synthesis, which is crucial for proliferating tumour cells.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25015460
- 003
- CZ-PrNML
- 005
- 20250731091008.0
- 007
- ta
- 008
- 250708e20250428fr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.biopha.2025.118096 $2 doi
- 035 __
- $a (PubMed)40300388
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a fr
- 100 1_
- $a Dilenko, Hanna $u Department of Medical Biophysics, Faculty of Medicine and Dentistry, Palacky University, Hněvotinska 3, Olomouc 77900, Czech Republic
- 245 10
- $a Illuminating the dark: PEGylated carboxylated graphene quantum dots and curcumin in nucleolar activity and PDT-induced DNA damage in cancer / $c H. Dilenko, K. Bartoň Tománková, E. Hinde, L. Válková, M. Kolaříková, H. Kolářová
- 520 9_
- $a Many photosensitive substances suitable for photodynamic therapy (PDT) have limited applications due to their insufficient solubility in polar solvents. Our research overcomes this challenge by means of nanotechnology in order to transform hydrophobic compounds into stable aqueous solutions, enabling them to use their full potential and unique properties in cancer therapy. In this study, the novel nano-composite cGQDs-PEG-curcumin was developed to overcome the insolubility of curcumin in water and its extraordinary efficacy in PDT was evaluated. Complex characterization was performed using high-resolution transmission electron microscopy (HR-TEM), FTIR, and UV-Vis spectroscopy. Further analysis involved fluorescence lifetime imaging (FLIM), and its cellular localization was mapped with confocal microscopy. In order to evaluate PDT effectiveness, cells treated with cGQDs-PEG-curcumin were irradiated with 5 J/cm2 of 414 nm light. After irradiation, cell viability assay, scanning electron microscopy (SEM), reactive oxygen species (ROS) detection, comet assay, and γH2AX-based DNA double-strand breaks (DSBs) detection were assessed and revealed a remarkable ability of the nano-composite to induce DNA damage after irradiation without ROS production. Our findings highlight the potential of cGQDs-PEG-curcumin as a cutting-edge PDT agent, capable of disrupting cell membrane and nucleolar integrity and impairing ribosomal synthesis, which is crucial for proliferating tumour cells.
- 650 12
- $a kurkumin $x farmakologie $x chemie $7 D003474
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a kvantové tečky $x chemie $7 D045663
- 650 12
- $a fotochemoterapie $x metody $7 D010778
- 650 12
- $a polyethylenglykoly $x chemie $x farmakologie $7 D011092
- 650 12
- $a poškození DNA $x účinky léků $7 D004249
- 650 _2
- $a reaktivní formy kyslíku $x metabolismus $7 D017382
- 650 12
- $a grafit $x chemie $x farmakologie $7 D006108
- 650 _2
- $a viabilita buněk $x účinky léků $7 D002470
- 650 12
- $a buněčné jadérko $x účinky léků $x metabolismus $7 D002466
- 650 _2
- $a nádorové buněčné linie $7 D045744
- 650 12
- $a nádory $x farmakoterapie $7 D009369
- 650 12
- $a fotosenzibilizující látky $x farmakologie $7 D017319
- 650 _2
- $a dvouřetězcové zlomy DNA $x účinky léků $7 D053903
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Bartoň Tománková, Kateřina $u Department of Medical Biophysics, Faculty of Medicine and Dentistry, Palacky University, Hněvotinska 3, Olomouc 77900, Czech Republic. Electronic address: katerina.barton@upol.cz
- 700 1_
- $a Hinde, Elizabeth $u School of Physics, David Caro Building, University of Melbourne, 18 Spencer Road, Parkville, VIC 3010, Australia
- 700 1_
- $a Válková, Lucie $u Department of Medical Biophysics, Faculty of Medicine and Dentistry, Palacky University, Hněvotinska 3, Olomouc 77900, Czech Republic
- 700 1_
- $a Kolaříková, Markéta $u Department of Medical Biophysics, Faculty of Medicine and Dentistry, Palacky University, Hněvotinska 3, Olomouc 77900, Czech Republic
- 700 1_
- $a Kolářová, Hana $u Department of Medical Biophysics, Faculty of Medicine and Dentistry, Palacky University, Hněvotinska 3, Olomouc 77900, Czech Republic
- 773 0_
- $w MED00005486 $t Biomedicine & pharmacotherapy $x 1950-6007 $g Roč. 187 (20250428), s. 118096
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/40300388 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250708 $b ABA008
- 991 __
- $a 20250731091003 $b ABA008
- 999 __
- $a ok $b bmc $g 2366349 $s 1252585
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 187 $c - $d 118096 $e 20250428 $i 1950-6007 $m Biomedicine & pharmacotherapy $n Biomed Pharmacother $x MED00005486
- LZP __
- $a Pubmed-20250708