From Melanocyte to Metastatic Malignant Melanoma

Malignant melanoma is one of the most aggressive malignancies in human and is responsible for almost 60% of lethal skin tumors. Its incidence has been increasing in white population in the past two decades. There is a complex interaction of environmental (exogenous) and endogenous, including genetic...

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Main Authors: Bizhan Bandarchi, Linglei Ma, Roya Navab, Arun Seth, Golnar Rasty
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Dermatology Research and Practice
Online Access:http://dx.doi.org/10.1155/2010/583748
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author Bizhan Bandarchi
Linglei Ma
Roya Navab
Arun Seth
Golnar Rasty
author_facet Bizhan Bandarchi
Linglei Ma
Roya Navab
Arun Seth
Golnar Rasty
author_sort Bizhan Bandarchi
collection DOAJ
description Malignant melanoma is one of the most aggressive malignancies in human and is responsible for almost 60% of lethal skin tumors. Its incidence has been increasing in white population in the past two decades. There is a complex interaction of environmental (exogenous) and endogenous, including genetic, risk factors in developing malignant melanoma. 8–12% of familial melanomas occur in a familial setting related to mutation of the CDKN2A gene that encodes p16. The aim of this is to briefly review the microanatomy and physiology of the melanocytes, epidemiology, risk factors, clinical presentation, historical classification and histopathology and, more in details, the most recent discoveries in biology and genetics of malignant melanoma. At the end, the final version of 2009 AJCC malignant melanoma staging and classification is presented.
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institution Kabale University
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publishDate 2010-01-01
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series Dermatology Research and Practice
spelling doaj-art-8d81892698d948ac8f9bbf1cd9d00acf2025-02-03T07:26:03ZengWileyDermatology Research and Practice1687-61051687-61132010-01-01201010.1155/2010/583748583748From Melanocyte to Metastatic Malignant MelanomaBizhan Bandarchi0Linglei Ma1Roya Navab2Arun Seth3Golnar Rasty4Department of Applied Molecular Oncology, Princess Margaret Hospital, Ontario Cancer Institute, University of Toronto, 7 Yorkview Drive, Toronto, ON, M2N 2R9, CanadaDepartment of Pathology, University of Michigan Hospital, University of Michigan, Michigan 48109-0602, USADepartment of Applied Molecular Oncology, Princess Margaret Hospital, Ontario Cancer Institute, University of Toronto, 7 Yorkview Drive, Toronto, ON, M2N 2R9, CanadaDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, M4N 3M5, CanadaDepartment of Laboratory Medicine and Pathobiology, University Health Network, University of Toronto, Toronto, M5G 2C4, CanadaMalignant melanoma is one of the most aggressive malignancies in human and is responsible for almost 60% of lethal skin tumors. Its incidence has been increasing in white population in the past two decades. There is a complex interaction of environmental (exogenous) and endogenous, including genetic, risk factors in developing malignant melanoma. 8–12% of familial melanomas occur in a familial setting related to mutation of the CDKN2A gene that encodes p16. The aim of this is to briefly review the microanatomy and physiology of the melanocytes, epidemiology, risk factors, clinical presentation, historical classification and histopathology and, more in details, the most recent discoveries in biology and genetics of malignant melanoma. At the end, the final version of 2009 AJCC malignant melanoma staging and classification is presented.http://dx.doi.org/10.1155/2010/583748
spellingShingle Bizhan Bandarchi
Linglei Ma
Roya Navab
Arun Seth
Golnar Rasty
From Melanocyte to Metastatic Malignant Melanoma
Dermatology Research and Practice
title From Melanocyte to Metastatic Malignant Melanoma
title_full From Melanocyte to Metastatic Malignant Melanoma
title_fullStr From Melanocyte to Metastatic Malignant Melanoma
title_full_unstemmed From Melanocyte to Metastatic Malignant Melanoma
title_short From Melanocyte to Metastatic Malignant Melanoma
title_sort from melanocyte to metastatic malignant melanoma
url http://dx.doi.org/10.1155/2010/583748
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