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Proteoglycans as Target for an Innovative Therapeutic Approach in Chondrosarcoma: Preclinical Proof of Concept
Molecular cancer therapeutics, 2016-11, Vol.15 (11), p.2575-2585
Peyrode, Caroline
Weber, Valérie
Voissière, Aurélien
Maisonial-Besset, Aurélie
Vidal, Aurélien
Auzeloux, Philippe
Gaumet, Vincent
Borel, Michèle
Dauplat, Marie-Mélanie
Quintana, Mercedes
Degoul, Françoise
Rédini, Françoise
Chezal, Jean-Michel
Miot-Noirault, Elisabeth
2016
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Peyrode, Caroline
Weber, Valérie
Voissière, Aurélien
Maisonial-Besset, Aurélie
Vidal, Aurélien
Auzeloux, Philippe
Gaumet, Vincent
Borel, Michèle
Dauplat, Marie-Mélanie
Quintana, Mercedes
Degoul, Françoise
Rédini, Françoise
Chezal, Jean-Michel
Miot-Noirault, Elisabeth
Titel
Proteoglycans as Target for an Innovative Therapeutic Approach in Chondrosarcoma: Preclinical Proof of Concept
Ist Teil von
Molecular cancer therapeutics, 2016-11, Vol.15 (11), p.2575-2585
Ort / Verlag
United States: American Association for Cancer Research
Erscheinungsjahr
2016
Quelle
MEDLINE
Beschreibungen/Notizen
To date, surgery remains the only option for the treatment of chondrosarcoma, which is radio- and chemoresistant due in part to its large extracellular matrix (ECM) and poor vascularity. In case of unresectable locally advanced or metastatic diseases with a poor prognosis, improving the management of chondrosarcoma still remains a challenge. Our team developed an attractive approach of improvement of the therapeutic index of chemotherapy by targeting proteoglycan (PG)-rich tissues using a quaternary ammonium (QA) function conjugated to melphalan (Mel). First of all, we demonstrated the crucial role of the QA carrier for binding to aggrecan by surface plasmon resonance. In the orthotopic model of Swarm rat chondrosarcoma, an in vivo biodistribution study of Mel and its QA derivative (Mel-QA), radiolabeled with tritium, showed rapid radioactivity accumulation in healthy cartilaginous tissues and tumor after [ H]-Mel-QA injection. The higher T/M ratio of the QA derivative suggests some advantage of QA-active targeting of chondrosarcoma. The antitumoral effects were characterized by tumor volume assessment, in vivo Tc-NTP 15-5 scintigraphic imaging of PGs, H-HRMAS NMR spectroscopy, and histology. The conjugation of a QA function to Mel did not hamper its in vivo efficiency and strongly improved the tolerability of Mel leading to a significant decrease of side effects (hematologic analyses and body weight monitoring). Thus, QA conjugation leads to a significant improvement of the therapeutic index, which is essential in oncology and enable repeated cycles of chemotherapy in patients with chondrosarcoma. Mol Cancer Ther; 15(11); 2575-85. ©2016 AACR.
Sprache
Englisch
Identifikatoren
ISSN: 1535-7163
eISSN: 1538-8514
DOI: 10.1158/1535-7163.MCT-16-0003
Titel-ID: cdi_hal_primary_oai_HAL_hal_01636341v1
Format
–
Schlagworte
Animals
,
Antineoplastic Agents - pharmacology
,
Bone Neoplasms - diagnosis
,
Bone Neoplasms - drug therapy
,
Bone Neoplasms - metabolism
,
Cell Line, Tumor
,
Chemical Sciences
,
Chondrosarcoma - diagnosis
,
Chondrosarcoma - drug therapy
,
Chondrosarcoma - metabolism
,
Disease Models, Animal
,
Drug Evaluation, Preclinical
,
Humans
,
Male
,
Medicinal Chemistry
,
Melphalan - chemistry
,
Melphalan - pharmacology
,
Molecular Imaging - methods
,
Optical Imaging - methods
,
Organic chemistry
,
Proteoglycans - metabolism
,
Quaternary Ammonium Compounds - chemistry
,
Radiochemistry
,
Rats
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