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The SRC Inhibitor Dasatinib Induces Stem Cell-Like Properties in Head and Neck Cancer Cells that are Effectively Counteracted by the Mithralog EC-8042.
Hermida-Prado, Francisco; Villaronga, M Ángeles; Granda-Díaz, Rocío; Del-Río-Ibisate, Nagore; Santos, Laura; Hermosilla, Maria Ana; Oro, Patricia; Allonca, Eva; Agorreta, Jackeline; Garmendia, Irati; Tornín, Juan; Perez-Escuredo, Jhudit; Fuente, Rocío; Montuenga, Luis M; Morís, Francisco; Rodrigo, Juan P; Rodríguez, René; García-Pedrero, Juana M.
Affiliation
  • Hermida-Prado F; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
  • Villaronga MÁ; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Granda-Díaz R; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
  • Del-Río-Ibisate N; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Santos L; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
  • Hermosilla MA; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Oro P; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
  • Allonca E; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Agorreta J; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
  • Garmendia I; EntreChem SL, Vivero Ciencias de la Salud, 33011 Oviedo, Spain.
  • Tornín J; EntreChem SL, Vivero Ciencias de la Salud, 33011 Oviedo, Spain.
  • Perez-Escuredo J; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
  • Fuente R; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Montuenga LM; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Morís F; Program in Solid Tumors, Center for Applied Medical Research (CIMA), Department of Pathology, Anatomy and Physiology, University of Navarra, and Navarra's Health Research Institute (IDISNA), 31008 Pamplona, Spain.
  • Rodrigo JP; Ciber de Cáncer, CIBERONC, 28029 Madrid, Spain.
  • Rodríguez R; Program in Solid Tumors, Center for Applied Medical Research (CIMA), Department of Pathology, Anatomy and Physiology, University of Navarra, and Navarra's Health Research Institute (IDISNA), 31008 Pamplona, Spain.
  • García-Pedrero JM; Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias; Instituto Universitario de Oncología del Principado de Asturias, University of Oviedo, 33011 Oviedo, Spain.
J Clin Med ; 8(8)2019 Aug 02.
Article in En | MEDLINE | ID: mdl-31382448
The frequent dysregulation of SRC family kinases (SFK) in multiple cancers prompted various inhibitors to be actively tested in preclinical and clinical trials. Disappointingly, dasatinib and saracatinib failed to demonstrate monotherapeutic efficacy in patients with head and neck squamous cell carcinomas (HNSCC). Deeper functional and mechanistic knowledge of the actions of these drugs is therefore needed to improve clinical outcome and to develop more efficient combinational strategies. Even though the SFK inhibitors dasatinib and saracatinib robustly blocked cell migration and invasion in HNSCC cell lines, this study unveils undesirable stem cell-promoting functions that could explain the lack of clinical efficacy in HNSCC patients. These deleterious effects were targeted by the mithramycin analog EC-8042 that efficiently eliminated cancer stem cells (CSC)-enriched tumorsphere cultures as well as tumor bulk cells and demonstrated potent antitumor activity in vivo. Furthermore, combination treatment of dasatinib with EC-8042 provided favorable complementary anti-proliferative, anti-invasive, and anti-CSC functions without any noticeable adverse interactions of both agents. These findings strongly support combinational strategies with EC-8042 for clinical testing in HNSCC patients. These data may have implications on ongoing dasatinib-based trials.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Med Year: 2019 Document type: Article Affiliation country: Spain Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Med Year: 2019 Document type: Article Affiliation country: Spain Country of publication: Switzerland