Synchrotron-based fourier-transform infrared micro-spectroscopy (SR-FTIRM) fingerprint of the small anionic molecule cobaltabis (dicarbollide) uptake in glioma stem cells

The anionic cobaltabis (dicarbollide) [3,3'-Co(1,2-CBH)] -, [ o -COSAN] -, is the most studied icosahedral metallacarborane. The sodium salts of [ o -COSAN] - could be an ideal candidate for the anti-cancer treatment Boron Neutron Capture Therapy (BNCT) as it possesses the ability to readily cr...

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Detalles Bibliográficos
Autores: Nuez-Martínez, Miquel, Pedrosa, Leire|||0000-0002-1852-4975, Martínez-Rovira, Immaculada|||0000-0002-2918-489X, Yousef, Ibraheem|||0000-0001-7818-8611, Diao, Diouldé, Teixidor, Francesc|||0000-0002-3010-2417, Stanzani, Elisabetta|||0000-0002-1787-7154, Martinez, Fina|||0000-0002-0940-1025, Tortosa, Avelina|||0000-0002-9080-2976, Sierra-Jimenez, Angels|||0000-0003-1023-3492, Gonzalez, José Juan, Viñas, Clara|||0000-0001-5000-0277
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:264931
Acceso en línea:https://ddd.uab.cat/record/264931
https://dx.doi.org/urn:doi:10.3390/ijms22189937
Access Level:acceso abierto
Palabra clave:Boron neutron capture therapy
Cobaltabis (dicarbollide)
DNA interactions
Glioblastoma
Glioma initiating cells
Inorganic small molecules
Lipid saturation
SR-FTIRM
Descripción
Sumario:The anionic cobaltabis (dicarbollide) [3,3'-Co(1,2-CBH)] -, [ o -COSAN] -, is the most studied icosahedral metallacarborane. The sodium salts of [ o -COSAN] - could be an ideal candidate for the anti-cancer treatment Boron Neutron Capture Therapy (BNCT) as it possesses the ability to readily cross biological membranes thereby producing cell cycle arrest in cancer cells. BNCT is a cancer therapy based on the potential of 10 B atoms to produce α particles that cross tissues in which the 10 B is accumulated without damaging the surrounding healthy tissues, after being irradiated with low energy thermal neutrons. Since Na[ o -COSAN] displays a strong and characteristic ν(B-H) frequency in the infrared range 2.600-2.500 cm -1, we studied the uptake of Na[ o -COSAN] followed by its interaction with biomolecules and its cellular biodistribution in two different glioma initiating cells (GICs), mesenchymal and proneural respectively, by using Synchrotron Radiation-Fourier Transform Infrared (FTIR) micro-spectroscopy (SR-FTIRM) facilities at the MIRAS Beamline of ALBA synchrotron light source. The spectroscopic data analysis from the bands in the regions of DNA, proteins, and lipids permitted to suggest that after its cellular uptake, Na[ o -COSAN] strongly interacts with DNA strings, modifies proteins secondary structure and also leads to lipid saturation. The mapping suggests the nuclear localization of [ o -COSAN] -, which according to reported Monte Carlo simulations may result in a more efficient cell-killing effect compared to that in a uniform distribution within the entire cell. In conclusion, we show pieces of evidence that at low doses, [ o -COSAN] - translocates GIC cells' membranes and it alters the physiology of the cells, suggesting that Na[ o -COSAN] is a promising agent to BNCT for glioblastoma cells.