Electrochemiluminescence assay for the impact of Ganoderma lucidum polysaccharides on resisting arsenic-induced apoptos… (2024)

1. Lu, Molecular mechanisms of bioactive polysaccharides from ganoderma lucidum (Lingzhi), a review, Int. J. Biol. Macromol., № 150, с. 765
   https://doi.org/10.1016/j.ijbiomac.2020.02.035
2. Milhorini, Antimelanoma effect of a fucoxylomannan isolated from Ganoderma lucidum fruiting bodies, Carbohydr. Polym., № 294
3. Xu, Effect of liquid fermented Chinese edible ganoderma lucidum fungus on wheat bread: a quality improver and staling inhibitor, Food Control, № 155
   https://doi.org/10.1016/j.foodcont.2023.110060
4. Camargo, Ganoderma lucidum polysaccharides inhibit in vitro tumorigenesis, cancer stem cell properties and epithelial-mesenchymal transition in oral squamous cell carcinoma, J. Ethnopharmacol., № 286
   https://doi.org/10.1016/j.jep.2021.114891
5. Li, Effects of drying methods on bioactive components of Ganoderma lucidumfermented whole wheat in products & in vitro digestive model, Food Res. Int., № 168
   https://doi.org/10.1016/j.foodres.2023.112641
6. Zhang, Recent advances in ganoderma lucidum polysaccharides: structures/bioactivities, biosynthesis and regulation, Food Biosci., № 56
   https://doi.org/10.1016/j.fbio.2023.103281
7. Wen, Structure of water-soluble polysaccharides in spore of Ganoderma lucidum and their anti-inflammatory activity, Food Chem., № 373
   https://doi.org/10.1016/j.foodchem.2021.131374
8. Liu, Hypoglycemic effect of inulin combined with ganoderma lucidum polysaccharides in T2DM rats, J. Funct. Foods, № 55, с. 381
   https://doi.org/10.1016/j.jff.2019.02.036
9. Li, Ganoderma lucidum polysaccharides ameliorated depression-like behaviors in the chronic social defeat stress depression model via modulation of Dectin-1 and the innate immune system, Brain Res. Bull., № 171, с. 16
   https://doi.org/10.1016/j.brainresbull.2021.03.002
10. Li, Ganoderma lucidum polysaccharide hydrogel accelerates diabetic wound healing by regulating macrophage polarization, Int. J. Biol. Macromol., № 260
    https://doi.org/10.1016/j.ijbiomac.2024.129682
11. Obeng, Apoptosis (programmed cell death) and its signals - a review, Braz. J. Biol., № 81, с. 1133
    https://doi.org/10.1590/1519-6984.228437
12. Erekat, Programmed cell death in diabetic nephropathy: a review of apoptosis, autophagy, and necroptosis, Med. Sci. Monit., № 28
    https://doi.org/10.12659/MSM.937766
13. D'Arcy, Cell death: a review of the major forms of apoptosis, necrosis and autophagy, Cell Biol. Int., № 43, с. 582
    https://doi.org/10.1002/cbin.11137
14. Geske, The biology of apoptosis, Hum. Pathol., № 32, с. 1029
    https://doi.org/10.1053/hupa.2001.28250
15. Niu, Lighting up the changes of plasma membranes during apoptosis with fluorescent probes, Coord. Chem. Rev., № 476
    https://doi.org/10.1016/j.ccr.2022.214926
16. Rana, Metals and apoptosis: recent developments, J. Trace Elem. Med. Biol., № 22, с. 262
    https://doi.org/10.1016/j.jtemb.2008.08.002
17. Erekat, Apoptosis and its therapeutic implications in neurodegenerative diseases, Clin. Anat., № 35, с. 65
    https://doi.org/10.1002/ca.23792
18. Bai, A caspase-3-activatable bimodal probe for photoacoustic and magneticresonance imaging of tumor apoptosis in vivo, Biosens. Bioelectron., № 216
    https://doi.org/10.1016/j.bios.2022.114648
19. Chang, Free fatty acids induce apoptosis of mammary epithelial cells of ketotic dairy cows via the mito-ROS/NLRP3 signaling pathway, J. Agric. Food Chem., № 71, с. 12645
    https://doi.org/10.1021/acs.jafc.3c02090
20. Kim, Titanium dioxide nanoparticles induce apoptosis by interfering with EGFR signaling in human breast cancer cells, Environ. Res., № 175, с. 117
    https://doi.org/10.1016/j.envres.2019.05.001
21. Abou-Zied, EGFR inhibitors and apoptotic inducers: design, synthesis, anticancer activity and docking studies of novel xanthine derivatives carrying chalcone moiety as hybrid molecules, Bioorg. Chem., № 89
    https://doi.org/10.1016/j.bioorg.2019.102997
22. Carneiro, Targeting apoptosis in cancer therapy, Nat. Rev. Clin. Oncol., № 17, с. 395
    https://doi.org/10.1038/s41571-020-0341-y
23. Renu, Molecular mechanism of heavy metals (lead, chromium, arsenic, mercury, nickel and cadmium) - induced hepatotoxicity - a review, Chemosphere, № 271
    https://doi.org/10.1016/j.chemosphere.2021.129735
24. Ozturk, Arsenic and human health: genotoxicity, epigenomic effects, and cancer signaling, Biol. Trace Elem. Res., № 200, с. 988
    https://doi.org/10.1007/s12011-021-02719-w
25. Wang, Therapeutic strategy of arsenic trioxide in the fight against cancers and other diseases, Metallomics, № 12, с. 326
    https://doi.org/10.1039/c9mt00308h
26. Sadaf, Arsenic trioxide induces apoptosis and inhibits the growth of human liver cancer cells, Life Sci., № 205, с. 9
    https://doi.org/10.1016/j.lfs.2018.05.006
27. Tang, Olaparib synergizes with arsenic trioxide by promoting apoptosis and ferroptosis in platinum-resistant ovarian cancer, Cell Death Dis., № 13, с. 826
    https://doi.org/10.1038/s41419-022-05257-y
28. Yu, Arsenic trioxide activates yes-associated protein by lysophosphatidic acid metabolism to selectively induce apoptosis of vascular smooth muscle cells, Biochim. Biophys. Acta Mol. Cell Res., № 1869
    https://doi.org/10.1016/j.bbamcr.2022.119211
29. Khosravani, Arsenic trioxide and Erlotinib loaded in RGD-modified nanoliposomes for targeted combination delivery to PC3 and PANC-1 cell lines, Biotechnol. Appl. Biochem., № 70, с. 811
    https://doi.org/10.1002/bab.2401
30. Khan, Glucogallin attenuates RAW 264.7 cells from arsenic trioxide induced toxicity via the NF-ҡB/NLRP3 pathway, Molecules, № 27, с. 5263
    https://doi.org/10.3390/molecules27165263
31. Huang, Honokiol attenuate the arsenic trioxide-induced cardiotoxicity by reducing the myocardial apoptosis, Pharmacol. Res. Perspect., № 10
    https://doi.org/10.1002/prp2.914
32. Peng, A tandem DNA nanomachines-supported electrochemiluminescence assay for attomolar detection of miRNA at ambient-temperature, Chem. Eng. J., № 480
    https://doi.org/10.1016/j.cej.2023.148161
33. Wei, Recent advances and challenges in developing electrochemiluminescence biosensors for health analysis, Chem. Commun., № 59, с. 3507
    https://doi.org/10.1039/D2CC06930J
34. Scarabelli, Towards Electrochemiluminescence microscopy exploration of plasmonic-mediated phenomena at the single-nanoparticle level, Angew. Chem. Int. Ed., № 62
    https://doi.org/10.1002/anie.202217614
35. Descamps, Ultrasensitive imaging of cells and sub-cellular entities by electrochemiluminescence, Angew. Chem. Int. Ed., № 62
    https://doi.org/10.1002/anie.202218574
36. Zhang, Recent progress in electrochemiluminescence microscopy analysis of single cells, Analyst, № 147, с. 2884
    https://doi.org/10.1039/D2AN00709F
37. Muzyka, Current trends in the development of the electrochemiluminescent immunosensors, Biosens. Bioelectron., № 54, с. 393
    https://doi.org/10.1016/j.bios.2013.11.011
38. Wang, Dual intramolecular electron transfer for in situ coreactant-embedded electrochemiluminescence microimaging of membrane protein, Angew. Chem. Int. Ed., № 60, с. 197
    https://doi.org/10.1002/anie.202011176
39. Liu, Single biomolecule imaging by electrochemiluminescence, J. Am. Chem. Soc., № 143, с. 17910
    https://doi.org/10.1021/jacs.1c06673
40. Dong, Direct imaging of single-molecule electrochemical reactions in solution, Nature, № 596, с. 244
    https://doi.org/10.1038/s41586-021-03715-9
41. Liu, Potential-resolved electrochemiluminescence nanoprobes for visual apoptosis evaluation at single-cell level, Anal. Chem., № 91, с. 6363
    https://doi.org/10.1021/acs.analchem.9b01401
42. Bommareddy, α-Santalol, a derivative of sandalwood oil, induces apoptosis in human prostate cancer cells by causing caspase-3 activation, Phytomedicine, № 19, с. 804
    https://doi.org/10.1016/j.phymed.2012.04.003

About this publication