http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019072885-A1

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filingDate 2018-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a0254a8c2bd35ef8a71df662efcd29c
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publicationDate 2019-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2019072885-A1
titleOfInvention MAGNETIC NANOPARTICLES FOR THE TREATMENT OF CANCER
abstract The present invention relates to methods and pharmaceutical compositions for the treatment of cancer in a subject in need of such treatment. Therapeutic strategies using drugs that cause death of lysosomal cells have been proposed for the eradication of resistant cancer cells. Magnetic nanoparticle (MNP) -based nano-therapy based on magnetic lysosomal hyperthermia (MILH) that is grafted with overexpressed receptor ligands into tumors appears to be a very promising therapeutic option. The inventors examined the mechanisms by which MILH induces cell death using gastrin-grafted MNP specifically administered to lysosomes of tumor cells of different cancers. The inventors demonstrate that MILH causes cell death via a non-apoptotic signaling pathway. The mechanism of cell death involves raising the temperature at the periphery of the nanoparticles that enhances the production of reactive oxygen species by the lysosomal Fenton reaction. Subsequently, MILH induces lipid peroxidation, permeabilization of the lysosomal membrane and leakage of lysosomal enzymes into the cytosol, including cathepsin-B which activates caspase-1 but not caspase-3. Thus, the invention relates to a magnetic nanoparticle grafted with a tumor targeting agent for use in a method for inducing non-apoptotic signaling of a cancer cell in a subject suffering from a cancer requiring such treatment.
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB7M0I7
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ7N4G1
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ7MM84
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB7LQP1
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB4TV14
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB4THD3
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Total number of triples: 2484.