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Nanodiamond modified copolymer scaffolds affects tumour progression of early neoplastic oral keratinocytes

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-188287
  • This study aimed to evaluate the tumorigenic potential of functionalising poly(LLA-co-CL) scaffolds. The copolymer scaffolds were functionalised with nanodiamonds (nDP) or with nDP and physisorbed BMP-2 (nDP-PHY) to enhance osteoinductivity. Culturing early neoplastic dysplastic keratinocytes (DOK\(^{Luc}\)) on nDP modified scaffolds reduced significantly their subsequent sphere formation ability and decreased significantly the cells' proliferation in the supra-basal layers of in vitro 3D oral neoplastic mucosa (3D-OT) when compared toThis study aimed to evaluate the tumorigenic potential of functionalising poly(LLA-co-CL) scaffolds. The copolymer scaffolds were functionalised with nanodiamonds (nDP) or with nDP and physisorbed BMP-2 (nDP-PHY) to enhance osteoinductivity. Culturing early neoplastic dysplastic keratinocytes (DOK\(^{Luc}\)) on nDP modified scaffolds reduced significantly their subsequent sphere formation ability and decreased significantly the cells' proliferation in the supra-basal layers of in vitro 3D oral neoplastic mucosa (3D-OT) when compared to DOK\(^{Luc}\) previously cultured on nDP-PHY scaffolds. Using an in vivo non-invasive environmentally-induced oral carcinogenesis model, nDP scaffolds were observed to reduce bioluminescence intensity of tumours formed by DOK\(^{Luc}\) + carcinoma associated fibroblasts (CAF). nDP modification was also found to promote differentiation of DOK\(^{Luc}\) both in vitro in 3D-OT and in vivo in xenografts formed by DOKLuc alone. The nDP-PHY scaffold had the highest number of invasive tumours formed by DOK\(^{Luc}\) + CAF outside the scaffold area compared to the nDP and control scaffolds. In conclusion, in vitro and in vivo results presented here demonstrate that nDP modified copolymer scaffolds are able to decrease the tumorigenic potential of DOK\(^{Luc}\), while confirming concerns for the therapeutic use of BMP-2 for reconstruction of bone defects in oral cancer patients due to its tumour promoting capabilities.zeige mehrzeige weniger

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Metadaten
Autor(en): Salwa Suliman, Kamal Mustafa, Anke Krueger, Doris Steinmüller-Nethl, Anna Finne-Wistrand, Tereza Osdal, Amani O. Hamza, Yang Sun, Himalaya Parajuli, Thilo Waag, Joachim Nickel, Anne Christine Johannessen, Emmet McCormack, Daniela Elena Costea
URN:urn:nbn:de:bvb:20-opus-188287
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Fakultät für Chemie und Pharmazie / Institut für Organische Chemie
Medizinische Fakultät / Lehrstuhl für Tissue Engineering und Regenerative Medizin
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Biomaterials
Erscheinungsjahr:2016
Band / Jahrgang:95
Seitenangabe:11-21
Originalveröffentlichung / Quelle:Biomaterials (2016) 95, 11-21. https://doi.org/10.1016/j.biomaterials.2016.04.002
DOI:https://doi.org/10.1016/j.biomaterials.2016.04.002
Allgemeine fachliche Zuordnung (DDC-Klassifikation):5 Naturwissenschaften und Mathematik / 54 Chemie / 547 Organische Chemie
6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):BMP-2; Biocompatibility; Biodegradable polymer scaffolds; Bone morphogenetic protein-2; Bone tissue engineering; Growth; BMP-2; In-vitro; Mandibular continuity defects; Marrow stromal cells; Mesenchymal transition; Microenvironment; Oral squamous cell carcinoma; Sinus floor augmentation; Squamous-cell carcinoma; Tumorigenicity
Datum der Freischaltung:04.06.2020
EU-Projektnummer / Contract (GA) number:242175-VascuBone
OpenAIRE:OpenAIRE
Lizenz (Deutsch):License LogoCC BY-NC-ND: Creative-Commons-Lizenz: Namensnennung, Nicht kommerziell, Keine Bearbeitungen 4.0 International