Premium
Targeting Innate Immunity with dsRNA‐Conjugated Mesoporous Silica Nanoparticles Promotes Antitumor Effects on Breast Cancer Cells
Author(s) -
Ultimo Amelia,
Giménez Cristina,
Bartovsky Pavel,
Aznar Elena,
Sancenón Félix,
Marcos M. Dolores,
Amorós Pedro,
Bernardo Ana R.,
MartínezMáñez Ramón,
JiménezLara Ana M.,
Murguía José R.
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201504629
Subject(s) - tlr3 , mesoporous silica , cancer cell , cytotoxic t cell , apoptosis , doxorubicin , innate immune system , chemistry , cytotoxicity , gene silencing , cancer research , mesoporous material , cancer , toll like receptor , receptor , biology , medicine , biochemistry , chemotherapy , in vitro , gene , catalysis
We describe herein a Toll‐like receptor 3 (TLR3) targeting delivery system based on mesoporous silica nanoparticles capped with the synthetic double stranded RNA polyinosinic–polycytidylic acid (poly(I:C)) for controlled cargo delivery in SK‐BR‐3 breast carcinoma cells. Our results show that poly(I:C)‐conjugated nanoparticles efficiently targeted breast cancer cells due to dsRNA–TLR3 interaction. Such interaction also triggered apoptotic pathways in SK‐BR‐3, significantly decreasing cells viability. Poly(I:C) cytotoxic effect in breast carcinoma cells was enhanced by loading nanoparticles′ mesopores with the anthracyclinic antibiotic doxorubicin, a commonly used chemotherapeutic agent.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom