Nanoplasmonic Single-Tumoroid Microarray for Real-Time Secretion Analysis.

Détails

ID Serval
serval:BIB_854452266478
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Nanoplasmonic Single-Tumoroid Microarray for Real-Time Secretion Analysis.
Périodique
Advanced science
Auteur⸱e⸱s
Liu Y.C., Ansaryan S., Tan J., Broguiere N., Lorenzo-Martín L.F., Homicsko K., Coukos G., Lütolf M.P., Altug H.
ISSN
2198-3844 (Electronic)
ISSN-L
2198-3844
Statut éditorial
Publié
Date de publication
09/2024
Peer-reviewed
Oui
Volume
11
Numéro
34
Pages
e2401539
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Organoid tumor models have emerged as a powerful tool in the fields of biology and medicine as such 3D structures grown from tumor cells recapitulate better tumor characteristics, making these tumoroids unique for personalized cancer research. Assessment of their functional behavior, particularly protein secretion, is of significant importance to provide comprehensive insights. Here, a label-free spectroscopic imaging platform is presented with advanced integrated optofluidic nanoplasmonic biosensor that enables real-time secretion analysis from single tumoroids. A novel two-layer microwell design isolates tumoroids, preventing signal interference, and the microarray configuration allows concurrent analysis of multiple tumoroids. The dual imaging capability combining time-lapse plasmonic spectroscopy and bright-field microscopy facilitates simultaneous observation of secretion dynamics, motility, and morphology. The integrated biosensor is demonstrated with colorectal tumoroids derived from both cell lines and patient samples to investigate their vascular endothelial growth factor A (VEGF-A) secretion, growth, and movement under various conditions, including normoxia, hypoxia, and drug treatment. This platform, by offering a label-free approach with nanophotonics to monitor tumoroids, can pave the way for new applications in fundamental biological studies, drug screening, and the development of therapies.
Mots-clé
Humans, Cell Line, Tumor, Vascular Endothelial Growth Factor A/metabolism, Vascular Endothelial Growth Factor A/genetics, Biosensing Techniques/methods, Organoids/metabolism, Colorectal Neoplasms/metabolism, microarray, microfluidics, nanohole array, nanophotonics, nanoplasmonic biosensor, protein secretion, tumoroids
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/06/2024 12:27
Dernière modification de la notice
11/10/2024 20:14
Données d'usage