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Emerging functions and clinical prospects of connexins and pannexins in melanoma.
Varela-Vázquez, Adrián; Guitián-Caamaño, Amanda; Carpintero-Fernandez, Paula; Fonseca, Eduardo; Sayedyahossein, Samar; Aasen, Trond; Penuela, Silvia; Mayán, María D.
Affiliation
  • Varela-Vázquez A; CellCOM Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, Xubias de Arriba, 84, 15006 A Coruña, Spain.
  • Guitián-Caamaño A; CellCOM Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, Xubias de Arriba, 84, 15006 A Coruña, Spain.
  • Carpintero-Fernandez P; CellCOM Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, Xubias de Arriba, 84, 15006 A Coruña, Spain.
  • Fonseca E; CellCOM Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, Xubias de Arriba, 84, 15006 A Coruña, Spain; Dermatology Deparment, University Hospital of A Coruña, Xubias de Arriba, 84, 15006 A Coruña, Spain.
  • Sayedyahossein S; Department of Anatomy & Cell Biology, and Oncology, Schulich School of Medicine and Dentistry, Western University, London, ON, N6A5C1, Canada.
  • Aasen T; Translational Molecular Pathology, Vall d'Hebron Institute of Research (VHIR), Autonomous University of Barcelona, CIBERONC, Barcelona, Spain.
  • Penuela S; Department of Anatomy & Cell Biology, and Oncology, Schulich School of Medicine and Dentistry, Western University, London, ON, N6A5C1, Canada.
  • Mayán MD; CellCOM Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, Xubias de Arriba, 84, 15006 A Coruña, Spain. Electronic address: Ma.Dolores.Mayan.Santos@sergas.es.
Biochim Biophys Acta Rev Cancer ; 1874(1): 188380, 2020 08.
Article in En | MEDLINE | ID: mdl-32461135
Cellular communication through gap junctions and hemichannels formed by connexins and through channels made by pannexins allows for metabolic cooperation and control of cellular activity and signalling. These channel proteins have been described to be tumour suppressors that regulate features such as cell death, proliferation and differentiation. However, they display cancer type-dependent and stage-dependent functions and may facilitate tumour progression through junctional and non-junctional pathways. The accumulated knowledge and emerging strategies to target connexins and pannexins are providing novel clinical opportunities for the treatment of cancer. Here, we provide an updated overview of the role of connexins and pannexins in malignant melanoma. We discuss how targeting of these channel proteins may be used to potentiate antitumour effects in therapeutic settings, including through improved immune-mediated tumour elimination.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin / Skin Neoplasms / Connexins / Antineoplastic Agents, Immunological / Melanoma Language: En Journal: Biochim Biophys Acta Rev Cancer Year: 2020 Document type: Article Affiliation country: Spain Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin / Skin Neoplasms / Connexins / Antineoplastic Agents, Immunological / Melanoma Language: En Journal: Biochim Biophys Acta Rev Cancer Year: 2020 Document type: Article Affiliation country: Spain Country of publication: Netherlands