Gold nanoparticles loaded TNF-? and CALNN peptide as a drug delivery system and promising therapeutic agent for breast cancer cells
dc.contributor.author | Jabir, Majid S. | |
dc.contributor.author | Abood, Noor A. | |
dc.contributor.author | Jawad, Marwa H. | |
dc.contributor.author | Öztürk, Kamile | |
dc.contributor.author | Kadhim, Haider | |
dc.contributor.author | Albukhaty, Salim | |
dc.contributor.author | Al-Shammari, Ahmed | |
dc.contributor.author | AlMalki, Faizah A. | |
dc.contributor.author | Albaqami, Jawaher | |
dc.contributor.author | Sulaiman, Ghassan M. | |
dc.date.accessioned | 2023-01-16T12:10:49Z | |
dc.date.available | 2023-01-16T12:10:49Z | |
dc.date.issued | 2022 | |
dc.department | Sabire Yazıcı Fen Edebiyat Fakültesi | |
dc.description.abstract | We investigated the anti-cancer properties of gold nanoparticles loaded TNF- and CALNN peptides, which we proposed as a potential drug delivery system using in vitro and in vivo models. The binding of GNPs-TNF- and GNPs-TNF-CALNN was characterized using a UV, ELISA and SEM analysis. The outcomes demonstrated that a novel drug delivery system had an anti-proliferative activity against breast cancer cell lines through a mechanism of apoptosis induction. In vivo model involved studying the cytotoxic influence of a drug delivery system GNPs, GNPs-TNF-? and GNPs-TNF-?-CALNN when applied to the transplanted AN-3 cell line. tumor sections were examined using microarray. In-vivo studies demonstrated that GNPs alone had less of a growth inhibitory effect on tumors implanted in mice when compared to GNPs-TNF–CALNN combined therapy. The cytotoxic assay showed that GNPs, GNPs-TNF-? and GNPs-TNF-?-CALNN exhibit selective toxicity towards cancer cells, inducing cell apoptosis through activation of caspase-3 and 7, p53 protein. | |
dc.identifier.doi | 10.1080/10667857.2022.2133073 | |
dc.identifier.endpage | 3166 | en_US |
dc.identifier.issn | 1066-7857 | |
dc.identifier.issue | 14 | en_US |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 3152 | en_US |
dc.identifier.uri | https:/dx.doi.org/10.1080/10667857.2022.2133073 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12451/9943 | |
dc.identifier.volume | 37 | en_US |
dc.identifier.wos | WOS:000867615300001 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | |
dc.publisher | Taylor and Francis Ltd. | |
dc.relation.ispartof | Materials Technology | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/embargoedAccess | |
dc.subject | Apoptosis | |
dc.subject | Breast Cancer | |
dc.subject | CALNN | |
dc.subject | Gold Nanoparticles | |
dc.subject | TNF- ? | |
dc.title | Gold nanoparticles loaded TNF-? and CALNN peptide as a drug delivery system and promising therapeutic agent for breast cancer cells | |
dc.type | Article |