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ORCID: https://orcid.org/0000-0002-0577-692X, Alegría Aravena, Nicolás
ORCID: https://orcid.org/0000-0002-5708-997X, Zelli, Veronica
ORCID: https://orcid.org/0000-0002-0047-2919, García Díaz, Andrés José
ORCID: https://orcid.org/0000-0002-4662-2185, Ramírez Castillejo, María del Carmen
ORCID: https://orcid.org/0000-0002-1877-3381, Tessitore, Alessandra
ORCID: https://orcid.org/0000-0002-7663-2210, Cabo de la Vega, Carlos de
ORCID: https://orcid.org/0000-0002-2144-0107, Landette Castillejos, Tomás
ORCID: https://orcid.org/0000-0001-9753-5295 and Festuccia, Claudio
ORCID: https://orcid.org/0000-0002-3463-6475
(2024).
General Direct Anticancer Effects of Deer Growing Antler Extract in Several Tumour Cell Lines, and Immune System-Mediated Effects in Xenograft Glioblastoma.
"Pharmaceutics", v. 16
(n. 5);
ISSN 1999-4923.
https://doi.org/10.3390/pharmaceutics16050610.
| Título: | General Direct Anticancer Effects of Deer Growing Antler Extract in Several Tumour Cell Lines, and Immune System-Mediated Effects in Xenograft Glioblastoma |
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| Autor/es: |
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| Tipo de Documento: | Artículo |
| Título de Revista/Publicación: | Pharmaceutics |
| Fecha: | 30 Abril 2024 |
| ISSN: | 1999-4923 |
| Volumen: | 16 |
| Número: | 5 |
| Materias: | |
| ODS: | |
| Palabras Clave Informales: | Anti-tumour activity; Cancer; Cell proliferation; Deer velvet antler; Glioblastoma multiforme; Immune tolerance; Ligand; Macrophages; Progression; Stem-cells; Suppressor-cells |
| Escuela: | E.T.S. de Ingeniería Agronómica, Alimentaria y de Biosistemas (UPM) |
| Departamento: | Biotecnología - Biología Vegetal |
| Licencias Creative Commons: | Reconocimiento - Sin obra derivada - No comercial |
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Deer antlers are the fastest growing tissue. Because they are based on proto-oncogenes, to avoid the risk of cancer, antlers evolved strong anticancer mechanisms, and thus their extract (DVA) is effective also against the few human tumours studied so far. We assessed whether DVA is a general anticancer compound by testing the direct effects in cells of different tumours: glioblastoma (GBM; lines U87MG and U251), colorectal (CRC; lines DLD-1, HT-29, SW480, and SW620), breast cancer (BRCA; lines MCF7, SKBR3, and PA00), and leukaemia (THP-1). DVA reduced the viability of tumours but not healthy cells (NHC; lines 293T and HaCaT). Mobility decreased at least for the longest test (72 h). Intraperitoneal/oral 200 mg DVA/kg administration in GBM xenograft mice for 28 d reduced tumour weight by 66.3% and 61.4% respectively, and it also reduced spleen weight (43.8%). In addition, tumours treated with DVA showed symptoms of liquefactive necrosis. Serum cytokines showed DVA up-regulated factors related to tumour fighting and down-regulated those related to inducing immune tolerance to the tumour. DVA shows general anticancer effects in the lines tested and, in GBM mice, also strong indirect effects apparently mediated by the immune system. DVA may contain a future anticancer medicine without secondary effects.
| ID de Registro: | 89851 |
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| Identificador DC: | https://oa.upm.es/89851/ |
| Identificador OAI: | oai:oa.upm.es:89851 |
| URL Portal Científico: | https://portalcientifico.upm.es/es/ipublic/item/10303007 |
| Identificador DOI: | 10.3390/pharmaceutics16050610 |
| URL Oficial: | https://www.mdpi.com/1999-4923/16/5/610 |
| Depositado por: | iMarina Portal Científico |
| Depositado el: | 08 Jul 2025 08:02 |
| Ultima Modificación: | 08 Jul 2025 08:02 |
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