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cancer xenograft Children: Item: Title: Abstract Children: Item: Title: Background: Item: Title: Results: Item: Title: Conclusions: Item: Title: Background Item: Title: Materials and methods Children: Item: Title: Reagents Item: Title: PEI–IONP synthesis Item: Title: Cell internalization Item: Title: Iron content Item: Title: Cytotoxicity Item: Title: ELISA Item: Title: Western blotting Item: Title: MDA-MB-231 cell migration Item: Title: qPCR-RT Item: Title: Animal experimentation Item: Title: Histological studies Item: Title: Statistical analysis Item: Title: Results and discussion Children: Item: Title: PEI–IONP synthesis, apMNKQ2 conjugation and chemical–physical characterization Item: Title: PEI–IONPs deliver the apMNKQ2 intracellularly Item: Title: Synergism of the PEI–IONPs and apMNKQ2 in repressing MDA-MB-231 cell migration in vitro Item: Title: The conjugated apMNKQ2 reverts the antitumor effect of PEI–IONPs in the MDA-MB-231 tumor model in vivo Item: Title: Conjugated apMNKQ2 synergizes with PEI–IONPs to impair the MDA-MB-231 tumor vasculature but it antagonizes the increase of tumor-infiltrating macrophages in vivo Item: Title: Conclusions Item: Title: Anchor 27 Item: Title: Acknowledgements Item: Title: References Info: Title: An electrostatically conjugated-functional MNK1 aptamer reverts the intrinsic antitumor effect of polyethyleneimine-coated iron oxide nanoparticles in vivo in a human triple-negative cancer xenograft Author: Vladimir Mulens-Arias Subject: Cancer Nanotechnology, https://doi.org/10.1186/s12645-023-00204-8 Keywords: Aptamer; MNK1; Polyethyleneimine-coated iron oxide nanoparticles; Antitumor effect Creator: Springer Producer: Acrobat Distiller 10.1.8 (Windows); modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (SPRINGER SBM; licensed version) CreationDate: Thu Oct 12 11:17:36 CEST 2023 ModDate: Sun Nov 19 02:49:38 CET 2023 ID: 0xd63ecf84733e3df04183717ec226d01c, 0x85d170ed5060cddf24db782ff5cfe3a1 Filters: FilterPipeline: FlateDecode 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