Acral lentiginous melanoma: Basic facts, biological characteristics and research perspectives of an understudied disease
Acral lentiginous melanoma is a histological subtype of cutaneous melanoma that occurs in the glabrous skin of the palms, soles and the nail unit. Although in some countries, particularly in Latin America, Africa and Asia, it represents the most frequently diagnosed subtype of the disease, it only r...
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Published in: | Pigment cell and melanoma research Vol. 34; no. 1; pp. 59 - 71 |
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01-01-2021
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Abstract | Acral lentiginous melanoma is a histological subtype of cutaneous melanoma that occurs in the glabrous skin of the palms, soles and the nail unit. Although in some countries, particularly in Latin America, Africa and Asia, it represents the most frequently diagnosed subtype of the disease, it only represents a small proportion of melanoma cases in European‐descent populations, which is partially why it has not been studied to the same extent as other forms of melanoma. As a result, its unique genomic drivers remain comparatively poorly explored, as well as its causes, with current evidence supporting a UV‐independent path to tumorigenesis. In this review, we discuss current knowledge of the aetiology and diagnostic criteria of acral lentiginous melanoma, as well as its epidemiological and histopathological characteristics. We also describe what is known about the genomic landscape of this disease and review the available biological models to explore potential therapeutic targets. |
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AbstractList | Acral lentiginous melanoma is a histological subtype of cutaneous melanoma that occurs in the glabrous skin of the palms, soles and the nail unit. Although in some countries, particularly in Latin America, Africa and Asia, it represents the most frequently diagnosed subtype of the disease, it only represents a small proportion of melanoma cases in European-descent populations, which is partially why it has not been studied to the same extent as other forms of melanoma. As a result, its unique genomic drivers remain comparatively poorly explored, as well as its causes, with current evidence supporting a UV-independent path to tumorigenesis. In this review, we discuss current knowledge of the aetiology and diagnostic criteria of acral lentiginous melanoma, as well as its epidemiological and histopathological characteristics. We also describe what is known about the genomic landscape of this disease and review the available biological models to explore potential therapeutic targets. Acral lentiginous melanoma is a histological subtype of cutaneous melanoma that occurs in the glabrous skin of the palms, soles and the nail unit. Although in some countries, particularly in Latin America, Africa and Asia, it represents the most frequently diagnosed subtype of the disease, it only represents a small proportion of melanoma cases in European-descent populations, which is partially why it has not been studied to the same extent as other forms of melanoma. As a result, its unique genomic drivers remain comparatively poorly explored, as well as its causes, with current evidence supporting a UV-independent path to tumorigenesis. In this review, we discuss current knowledge of the aetiology and diagnostic criteria of acral lentiginous melanoma, as well as its epidemiological and histopathological characteristics. We also describe what is known about the genomic landscape of this disease and review the available biological models to explore potential therapeutic targets.Acral lentiginous melanoma is a histological subtype of cutaneous melanoma that occurs in the glabrous skin of the palms, soles and the nail unit. Although in some countries, particularly in Latin America, Africa and Asia, it represents the most frequently diagnosed subtype of the disease, it only represents a small proportion of melanoma cases in European-descent populations, which is partially why it has not been studied to the same extent as other forms of melanoma. As a result, its unique genomic drivers remain comparatively poorly explored, as well as its causes, with current evidence supporting a UV-independent path to tumorigenesis. In this review, we discuss current knowledge of the aetiology and diagnostic criteria of acral lentiginous melanoma, as well as its epidemiological and histopathological characteristics. We also describe what is known about the genomic landscape of this disease and review the available biological models to explore potential therapeutic targets. |
Author | Molina‐Aguilar, Christian Martínez‐Said, Héctor Adams, David J. Possik, Patricia A. Vázquez‐Cruz, Martha Estefania Roldán‐Marín, Rodrigo Robles‐Espinoza, Carla Daniela Garcia‐Salinas, Omar Isaac Basurto‐Lozada, Patricia Castaneda‐Garcia, Carolina Álvarez‐Cano, Alethia |
AuthorAffiliation | 5 Dermato‐Oncology Clinic Unidad de Medicina Experimental Facultad de Medicina Universidad Nacional Autónoma de México Mexico City Mexico 6 Program of Immunology and Tumor Biology Brazilian National Cancer Institute (INCA) Rio de Janeiro Brazil 3 Wellcome Sanger Institute Hinxton Cambridgeshire CB101SA UK 1 Laboratorio Internacional de Investigación Sobre el Genoma Humano Universidad Nacional Autónoma de México Santiago de Querétaro Mexico 2 Tecnologico de Monterrey School of Engineering and Sciences Centre of Bioengineering Querétaro Mexico 4 Instituto Nacional de Cancerología (INCan) Mexico City Mexico |
AuthorAffiliation_xml | – name: 6 Program of Immunology and Tumor Biology Brazilian National Cancer Institute (INCA) Rio de Janeiro Brazil – name: 1 Laboratorio Internacional de Investigación Sobre el Genoma Humano Universidad Nacional Autónoma de México Santiago de Querétaro Mexico – name: 3 Wellcome Sanger Institute Hinxton Cambridgeshire CB101SA UK – name: 4 Instituto Nacional de Cancerología (INCan) Mexico City Mexico – name: 2 Tecnologico de Monterrey School of Engineering and Sciences Centre of Bioengineering Querétaro Mexico – name: 5 Dermato‐Oncology Clinic Unidad de Medicina Experimental Facultad de Medicina Universidad Nacional Autónoma de México Mexico City Mexico |
Author_xml | – sequence: 1 givenname: Patricia surname: Basurto‐Lozada fullname: Basurto‐Lozada, Patricia organization: Universidad Nacional Autónoma de México – sequence: 2 givenname: Christian surname: Molina‐Aguilar fullname: Molina‐Aguilar, Christian organization: Centre of Bioengineering – sequence: 3 givenname: Carolina surname: Castaneda‐Garcia fullname: Castaneda‐Garcia, Carolina organization: Universidad Nacional Autónoma de México – sequence: 4 givenname: Martha Estefania surname: Vázquez‐Cruz fullname: Vázquez‐Cruz, Martha Estefania organization: Universidad Nacional Autónoma de México – sequence: 5 givenname: Omar Isaac surname: Garcia‐Salinas fullname: Garcia‐Salinas, Omar Isaac organization: Wellcome Sanger Institute – sequence: 6 givenname: Alethia surname: Álvarez‐Cano fullname: Álvarez‐Cano, Alethia organization: Instituto Nacional de Cancerología (INCan) – sequence: 7 givenname: Héctor surname: Martínez‐Said fullname: Martínez‐Said, Héctor organization: Instituto Nacional de Cancerología (INCan) – sequence: 8 givenname: Rodrigo surname: Roldán‐Marín fullname: Roldán‐Marín, Rodrigo organization: Universidad Nacional Autónoma de México – sequence: 9 givenname: David J. orcidid: 0000-0001-9490-0306 surname: Adams fullname: Adams, David J. organization: Wellcome Sanger Institute – sequence: 10 givenname: Patricia A. orcidid: 0000-0003-2899-0969 surname: Possik fullname: Possik, Patricia A. email: ppossik@inca.gov.br organization: Brazilian National Cancer Institute (INCA) – sequence: 11 givenname: Carla Daniela orcidid: 0000-0003-3277-7466 surname: Robles‐Espinoza fullname: Robles‐Espinoza, Carla Daniela email: drobles@liigh.unam.mx organization: Wellcome Sanger Institute |
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Copyright | 2020 The Authors. published by John Wiley & Sons Ltd. 2020 The Authors. Pigment Cell & Melanoma Research published by John Wiley & Sons Ltd. 2020. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | microenvironment epidemiology diagnosis genomics acral melanoma |
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Notes | Funding information This work was supported by the Wellcome Trust [204562/Z/16/Z to C.D.R.‐E.], Cancer Research UK [to D.J.A.], the Medical Research Council [MR/S01473X/1 to C.D.R.‐E., P.A.P. and D.J.A] and Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica (PAPIIT UNAM) [IA202020 to C.D.R.‐E.]. C.D.R.‐E. is also supported by CONACyT [A3‐S‐31603 and A1‐S‐30165], the Academy of Medical Sciences through a Newton Advanced Fellowship [NAF\R2\180782] and a Wellcome Sanger Institute International Fellowship. P.B.L. is a PhD student from Doctorado en Ciencias Biológicas, Universidad Nacional Autónoma de México (UNAM), and is supported by CONACyT. C.C.G. is a PhD student from Programa de Doctorado en Ciencias Biomédicas, Universidad Nacional Autónoma de México (UNAM), and is supported by CONACyT [scholarship no. 385365]. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
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SubjectTerms | acral melanoma Biological models (mathematics) diagnosis Diagnostic systems Epidemiology Foot Diseases - pathology genomics Humans Melanocytes - pathology Melanoma Melanoma - pathology microenvironment Nail Diseases - pathology Review Reviews Skin Neoplasms - pathology Tumorigenesis |
Title | Acral lentiginous melanoma: Basic facts, biological characteristics and research perspectives of an understudied disease |
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