Your browser doesn't support javascript.
loading
New CXCR1/CXCR2 inhibitors represent an effective treatment for kidney or head and neck cancers sensitive or refractory to reference treatments.
Dufies, Maeva; Grytsai, Oleksandr; Ronco, Cyril; Camara, Oumar; Ambrosetti, Damien; Hagege, Anaïs; Parola, Julien; Mateo, Lou; Ayrault, Marion; Giuliano, Sandy; Grépin, Renaud; Lagarde, Nathalie; Montes, Matthieu; Auberger, Patrick; Demange, Luc; Benhida, Rachid; Pagès, Gilles.
Afiliación
  • Dufies M; Centre Scientifique de Monaco, Biomedical Department, Principality of Monaco.
  • Grytsai O; Université Côte d'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
  • Ronco C; Université Côte d'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
  • Camara O; Université Côte d'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
  • Ambrosetti D; Université Côte d'Azur, Centre Hospitalier Universitaire (CHU) de Nice, Hôpital Pasteur, Department of Pathology, Nice, France.
  • Hagege A; Université Côte d'Azur, CNRS UMR 7284 and INSERM U 1081, Institute for Research on Cancer and Aging (IRCAN), 28 Avenue de Valombrose, 06107 Nice, France.
  • Parola J; Université Côte d'Azur, CNRS UMR 7284 and INSERM U 1081, Institute for Research on Cancer and Aging (IRCAN), 28 Avenue de Valombrose, 06107 Nice, France.
  • Mateo L; Centre Antoine Lacassagne, Nice, France.
  • Ayrault M; Université Côte d'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
  • Giuliano S; Université de Paris, CiTCoM, UMR 8038 CNRS, F-75006 Paris, France.
  • Grépin R; Université Côte d'Azur, CNRS UMR 7284 and INSERM U 1081, Institute for Research on Cancer and Aging (IRCAN), 28 Avenue de Valombrose, 06107 Nice, France.
  • Lagarde N; Centre Scientifique de Monaco, Biomedical Department, Principality of Monaco.
  • Montes M; Laboratoire GBCM EA7528, Conservatoire National des Arts et Métiers, 2 Rue Conté, 75003 Paris, France.
  • Auberger P; Laboratoire GBCM EA7528, Conservatoire National des Arts et Métiers, 2 Rue Conté, 75003 Paris, France.
  • Demange L; Université Côte d'Azur, INSERM U1065, Centre Méditerranéen de Médecine Moléculaire (C3M), Bâtiment ARCHIMED, 151 Route de Saint-Antoine de Ginestière, BP 2 3194, 06204 Nice Cedex 3, France.
  • Benhida R; Université Côte d'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
  • Pagès G; Université de Paris, CiTCoM, UMR 8038 CNRS, F-75006 Paris, France.
Theranostics ; 9(18): 5332-5346, 2019.
Article en En | MEDLINE | ID: mdl-31410218
Clear cell Renal Cell (RCC) and Head and Neck Squamous Cell Carcinomas (HNSCC) are characterized by a pro-angiogenic/pro-inflammatory context. Despite conventional or targeted therapies, metastatic RCC and HNSCC remain incurable. Alternative treatments to reference therapies (sunitinib, a multi tyrosine kinase inhibitor for RCC or cisplatin for HNSCC) are urgently needed on relapse. Here, we described the relevance of targeting the ELR+CXCL cytokines receptors, CXCR1/2, for the treatment of these two cancer types. Methods: The relevance to patient treatment was evaluated by correlating the ELR+CXCL/CXCR1/2 levels to survival using online available data. We report herein the synthesis of new pharmacological inhibitors of CXCR1/2 with anti-proliferation/survival activity. The latter was evaluated with the XTT assay with leukemic, breast, RCC and HNSCC cell lines. Their relevance as an alternative treatment was tested on sunitinib- and cisplatin- resistant cells. The most efficient compound was then tested in a mouse model of RCC and HNSCC. Results: RCC and HNSCC expressed the highest amounts of CXCR1/2 of all cancers. High levels of ELR+CXCL cytokines (CXCL1, 2, 3, 5, 6, 7, 8) correlated to shorter survival. Among the 33 synthesized and tested molecules, compound C29 reduced ELR+CXCL/CXCR1/2-dependent proliferation and migration of endothelial cells. C29 exerted an anti-proliferation/survival activity on a panel of cancer cells including naive and resistant RCC and HNSCC cells. C29 reduced the growth of experimental RCC and HNSCC tumors by decreasing tumor cell proliferation, angiogenesis and ELR+/CXCL-mediated inflammation. Conclusion: Our study highlights the relevance of new CXCR1/2 inhibitors for the treatment of RCC or HNSCC as first-line treatment or at relapse on reference therapies.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Interleucina-8A / Receptores de Interleucina-8B / Neoplasias de Cabeza y Cuello / Neoplasias Renales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Theranostics Año: 2019 Tipo del documento: Article Pais de publicación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Interleucina-8A / Receptores de Interleucina-8B / Neoplasias de Cabeza y Cuello / Neoplasias Renales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Theranostics Año: 2019 Tipo del documento: Article Pais de publicación: Australia