In vitro and in vivo antitumor effects of the VO-chrysin complex on a new three-dimensional osteosarcoma spheroids model and a xenograft tumor in mice
Autor: | J. F. Cadavid-Vargas, Cecilia Carbone, Fabricio Alejandro Maschi, Agustina Resasco, Ignacio E. León, Miguel Ángel Ayala, Susana B. Etcheverry |
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Rok vydání: | 2016 |
Předmět: |
Male
Bioquímica 0301 basic medicine Time Factors Cell Survival Otras Ciencias Biológicas Cell Culture Techniques Mice Nude Bone Neoplasms Biochemistry Ciencias Biológicas Inorganic Chemistry 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Coordination Complexes In vivo Cell Line Tumor Spheroids Cellular medicine Animals Humans Microscopy Phase-Contrast Chrysin Viability assay Flavonoids Osteosarcoma Molecular Structure Spheroid Vanadium Xenograft mice medicine.disease Xenograft Model Antitumor Assays Primary tumor In vitro Treatment Outcome 030104 developmental biology chemistry 030220 oncology & carcinogenesis Toxicity Cancer research Female Spheroids CIENCIAS NATURALES Y EXACTAS |
Zdroj: | SEDICI (UNLP) Universidad Nacional de La Plata instacron:UNLP |
ISSN: | 1432-1327 0949-8257 |
DOI: | 10.1007/s00775-016-1397-0 |
Popis: | Osteosarcoma (OS) is the most common primary tumor of bone, occurring predominantly in the second decade of life. High-dose cytotoxic chemotherapy and surgical resection have improved prognosis, with long-term survival for patients with localized disease. Vanadium is an ultra-trace element that after being absorbed accumulates in bone. Besides, vanadium compounds have been studied during recent years to be considered as representative of a new class of non-platinum antitumor agents. Moreover, flavonoids are a wide family of polyphenolic compounds that display many interesting biological effects. Since coordination of ligands to metals can improve the pharmacological properties, we report herein, for the first time, the in vitro and in vivo effects of an oxidovanadium(IV) complex with the flavonoid chrysin on the new 3D human osteosarcoma and xenograft osteosarcoma mice models. The pharmacological results show that VOchrys inhibited the cell viability affecting the shape and volume of the spheroids and VOchrys suppressed MG-63 tumor growth in the nude mice without inducing toxicity and side effects. As a whole, the results presented herein demonstrate that the antitumor action of the complex was very promissory on human osteosarcoma models, whereby suggesting that VOchrys is a potentially good candidate for future use in alternative antitumor treatments. Facultad de Ciencias Exactas Centro de Química Inorgánica Facultad de Ciencias Veterinarias |
Databáze: | OpenAIRE |
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