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Integrin alpha9 emerges as a key therapeutic target to reduce metastasis in rhabdomyosarcoma and neuroblastoma

The majority of current cancer therapies are aimed at reducing tumour growth, but there is lack of viable pharmacological options to reduce the formation of metastasis. This is a paradox, since more than 90% of cancer deaths are attributable to metastatic progression. Integrin alpha9 (ITGA9) has bee...

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Detalles Bibliográficos
Autores principales: Navarro, Natalia, Molist, Carla, Sansa-Girona, Júlia, Zarzosa, Patricia, Gallo-Oller, Gabriel, Pons, Guillem, Magdaleno, Ainara, Guillén, Gabriela, Hladun, Raquel, Garrido, Marta, Segura, Miguel F., Hontecillas-Prieto, Lourdes, de Álava, Enrique, Ponsati, Berta, Fernández-Carneado, Jimena, Almazán-Moga, Ana, Vallès-Miret, Mariona, Farrera-Sinfreu, Josep, de Toledo, Josep Sánchez, Moreno, Lucas, Gallego, Soledad, Roma, Josep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553833/
https://www.ncbi.nlm.nih.gov/pubmed/36221013
http://dx.doi.org/10.1007/s00018-022-04557-y
Descripción
Sumario:The majority of current cancer therapies are aimed at reducing tumour growth, but there is lack of viable pharmacological options to reduce the formation of metastasis. This is a paradox, since more than 90% of cancer deaths are attributable to metastatic progression. Integrin alpha9 (ITGA9) has been previously described as playing an essential role in metastasis; however, little is known about the mechanism that links this protein to this process, being one of the less studied integrins. We have now deciphered the importance of ITGA9 in metastasis and provide evidence demonstrating its essentiality for metastatic dissemination in rhabdomyosarcoma and neuroblastoma. However, the most translational advance of this study is to reveal, for the first time, the possibility of reducing metastasis by pharmacological inhibition of ITGA9 with a synthetic peptide simulating a key interaction domain of ADAM proteins, in experimental metastasis models, not only in childhood cancers but also in a breast cancer model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04557-y.