Anti-tumour activity of deer growing antlers and its potential applications in the treatment of malignant gliomas

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作者
Louis Chonco
Tomás Landete-Castillejos
Gemma Serrano-Heras
Martina Pérez Serrano
Francisco Javier Pérez-Barbería
Carlos González-Armesto
Andrés García
Carlos de Cabo
Jose Manuel Lorenzo
Chunyi Li
Tomás Segura
机构
[1] Complejo Hospitalario Universitario de Albacete,Research Unit
[2] Universidad de Castilla-La Mancha,Animal Science Techniques Applied to Wildlife Management Research Group, Instituto de Investigación en Recursos Cinegéticos
[3] Universidad de Castilla-La Mancha,Sección de Recursos Cinegéticos y Ganaderos, Instituto de Desarrollo Regional
[4] Universidad de Castilla-La Mancha,Departamento de Ciencia y Tecnología Agroforestal y Genética, Escuela Técnica Superior de Ingenieros Agrónomos y Montes
[5] Complejo Hospitalario Universitario de Albacete,Research Department, Neuropsychopharmacology Unit
[6] Centro Tecnológico de la Carne de Galicia,Área de Tecnología de los Alimentos, Facultad de Ciencias de Ourense
[7] Universidad de Vigo,Institute of Antler Science and Product Technology
[8] Changchun Sci-Tech University,Department of Neurology
[9] Complejo Hospitalario Universitario de Albacete,undefined
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A recent study showed that antlers have evolved a high rate of growth due to the expression of proto-oncogenes and that they have also evolved to express several tumour suppressor genes to control the risk of cancer. This may explain why deer antler velvet (DAV) extract shows anti-tumour activity. The fast growth of antler innervation through the velvet in close association to blood vessels provides a unique environment to study the fast but non-cancerous proliferation of heterogeneous cell populations. We set out to study the anti-cancer effect of DAV in glioblastoma (GB) cell lines in comparison with temozolomide, a chemotherapeutic drug used to treat high-grade brain tumours. Here we report, for the first time, that DAV extract from the tip, but not from mid-parts of the antler, exhibits an anti-tumour effect in GB cell lines (T98G and A172) while being non-toxic in non-cancerous cell lines (HEK293 and HACAT). In T98G cells, DAV treatment showed reduced proliferation (37.5%) and colony-formation capacity (84%), inhibited migration (39%), induced changes in cell cycle progression, and promoted apoptosis. The anticancer activity of DAV extract as demonstrated by these results may provide a new therapeutic strategy for GB treatment.
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