-
Je něco špatně v tomto záznamu ?
Selective Glycopolymer Inhibitors of Galectin-3: Supportive Anti-Cancer Agents Protecting Monocytes and Preserving Interferon-Gamma Function
M. Filipová, MR. Tavares, M. Hovorková, V. Heine, P. Nekvasilová, V. Křen, T. Etrych, P. Chytil, P. Bojarová
Jazyk angličtina Země Nový Zéland
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2012-01-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2009-01-01
Taylor & Francis Open Access
od 2006-09-01
Medline Complete (EBSCOhost)
od 2012-01-01
Health & Medicine (ProQuest)
od 2012-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
PubMed
40438186
DOI
10.2147/ijn.s503381
Knihovny.cz E-zdroje
- MeSH
- akrylamidy chemie farmakologie MeSH
- apoptóza účinky léků MeSH
- galektin 3 * antagonisté a inhibitory MeSH
- galektiny MeSH
- interferon gama * metabolismus MeSH
- krevní proteiny MeSH
- lidé MeSH
- makrofágy účinky léků MeSH
- monocyty * účinky léků MeSH
- nádorové mikroprostředí účinky léků MeSH
- polymery * chemie farmakologie MeSH
- protinádorové látky * farmakologie chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
INTRODUCTION: The immunosuppressive roles of galectin-3 (Gal-3) in carcinogenesis make this lectin an attractive target for pharmacological inhibition in immunotherapy. Although current clinical immunotherapies appear promising in the treatment of solid tumors, their efficacy is significantly weakened by the hostile immunosuppressive tumor microenvironment (TME). Gal-3, a prominent TME modulator, efficiently subverts the elimination of cancer, either directly by inducing apoptosis of immune cells or indirectly by binding essential effector molecules, such as interferon-gamma (IFNγ). METHODS: N-(2-Hydroxypropyl)methacrylamide (HPMA)-based glycopolymers bearing poly-N-acetyllactosamine-derived tetrasaccharide ligands of Gal-3 were designed, synthesized, and characterized using high-performance liquid chromatography, dynamic light scattering, UV-Vis spectrophotometry, gel permeation chromatography, nuclear magnetic resonance, high-resolution mass spectrometry and CCK-8 assay for evaluation of glycopolymer non-toxicity. Pro-immunogenic effects of purified glycopolymers were tested by apoptotic assay using flow cytometry, competitive ELISA, and in vitro cell-free INFγ-based assay. RESULTS: All tested glycopolymers completely inhibited Gal-3-induced apoptosis of monocytes/macrophages, of which the M1 subtype is responsible for eliminating cancer cells during immunotherapy. Moreover, the glycopolymers suppressed Gal-3-induced capture of glycosylated IFNγ by competitive inhibition to Gal-3 carbohydrate recognition domain (CRD), which enables further inherent biological activities of this effector, such as differentiation of monocytes into M1 macrophages and repolarization of M2-macrophages to the M1 state. CONCLUSION: The prepared glycopolymers are promising inhibitors of Gal-3 and may serve as important supportive anti-cancer nanosystems enabling the infiltration of proinflammatory macrophages and the reprogramming of unwanted M2 macrophages into the M1 subtype.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25015668
- 003
- CZ-PrNML
- 005
- 20250731091147.0
- 007
- ta
- 008
- 250708e20250524nz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.2147/IJN.S503381 $2 doi
- 035 __
- $a (PubMed)40438186
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a nz
- 100 1_
- $a Filipová, Marcela $u Department of Biological Models, Institute of Macromolecular Chemistry of the Czech Academy of Sciences, Prague, Czech Republic $1 https://orcid.org/0000000335037973
- 245 10
- $a Selective Glycopolymer Inhibitors of Galectin-3: Supportive Anti-Cancer Agents Protecting Monocytes and Preserving Interferon-Gamma Function / $c M. Filipová, MR. Tavares, M. Hovorková, V. Heine, P. Nekvasilová, V. Křen, T. Etrych, P. Chytil, P. Bojarová
- 520 9_
- $a INTRODUCTION: The immunosuppressive roles of galectin-3 (Gal-3) in carcinogenesis make this lectin an attractive target for pharmacological inhibition in immunotherapy. Although current clinical immunotherapies appear promising in the treatment of solid tumors, their efficacy is significantly weakened by the hostile immunosuppressive tumor microenvironment (TME). Gal-3, a prominent TME modulator, efficiently subverts the elimination of cancer, either directly by inducing apoptosis of immune cells or indirectly by binding essential effector molecules, such as interferon-gamma (IFNγ). METHODS: N-(2-Hydroxypropyl)methacrylamide (HPMA)-based glycopolymers bearing poly-N-acetyllactosamine-derived tetrasaccharide ligands of Gal-3 were designed, synthesized, and characterized using high-performance liquid chromatography, dynamic light scattering, UV-Vis spectrophotometry, gel permeation chromatography, nuclear magnetic resonance, high-resolution mass spectrometry and CCK-8 assay for evaluation of glycopolymer non-toxicity. Pro-immunogenic effects of purified glycopolymers were tested by apoptotic assay using flow cytometry, competitive ELISA, and in vitro cell-free INFγ-based assay. RESULTS: All tested glycopolymers completely inhibited Gal-3-induced apoptosis of monocytes/macrophages, of which the M1 subtype is responsible for eliminating cancer cells during immunotherapy. Moreover, the glycopolymers suppressed Gal-3-induced capture of glycosylated IFNγ by competitive inhibition to Gal-3 carbohydrate recognition domain (CRD), which enables further inherent biological activities of this effector, such as differentiation of monocytes into M1 macrophages and repolarization of M2-macrophages to the M1 state. CONCLUSION: The prepared glycopolymers are promising inhibitors of Gal-3 and may serve as important supportive anti-cancer nanosystems enabling the infiltration of proinflammatory macrophages and the reprogramming of unwanted M2 macrophages into the M1 subtype.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a interferon gama $x metabolismus $7 D007371
- 650 12
- $a monocyty $x účinky léků $7 D009000
- 650 12
- $a galektin 3 $x antagonisté a inhibitory $7 D037502
- 650 _2
- $a apoptóza $x účinky léků $7 D017209
- 650 12
- $a protinádorové látky $x farmakologie $x chemie $7 D000970
- 650 _2
- $a makrofágy $x účinky léků $7 D008264
- 650 _2
- $a nádorové mikroprostředí $x účinky léků $7 D059016
- 650 _2
- $a akrylamidy $x chemie $x farmakologie $7 D000178
- 650 12
- $a polymery $x chemie $x farmakologie $7 D011108
- 650 _2
- $a krevní proteiny $7 D001798
- 650 _2
- $a galektiny $7 D037161
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Tavares, Marina Rodrigues $u Department of Biomedical Polymers, Institute of Macromolecular Chemistry of the Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Hovorková, Michaela $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic $1 https://orcid.org/0000000303707936
- 700 1_
- $a Heine, Viktoria $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Nekvasilová, Pavlína $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic
- 700 1_
- $a Křen, Vladimír $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Etrych, Tomáš $u Department of Biomedical Polymers, Institute of Macromolecular Chemistry of the Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Chytil, Petr $u Department of Biomedical Polymers, Institute of Macromolecular Chemistry of the Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Bojarová, Pavla $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic $u Department of Health Care Disciplines and Population Protection, Faculty of Biomedical Engineering, Czech Technical University in Prague, Kladno, Czech Republic
- 773 0_
- $w MED00176143 $t International journal of nanomedicine $x 1178-2013 $g Roč. 20 (20250524), s. 6591-6609
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/40438186 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250708 $b ABA008
- 991 __
- $a 20250731091142 $b ABA008
- 999 __
- $a ok $b bmc $g 2366493 $s 1252793
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 20 $c - $d 6591-6609 $e 20250524 $i 1178-2013 $m International journal of nanomedicine $n Int J Nanomedicine $x MED00176143
- LZP __
- $a Pubmed-20250708