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PMID: 27155159 Published · ppublish English Journal Article Review

Multiple roles of NF1 in the melanocyte lineage.

Pigment cell & melanoma research ·Vol. 29 ·No. 4 ·2016-00-00 ·页码 417-25

Larribère L, Utikal J

Abstract

NF1 is a tumour suppressor gene, germline mutations of which lead to neurofibromatosis type 1 syndrome. Patients develop benign tumours from several types of cells including neural crest-derived cells. NF1 somatic mutations also occur in 15% of sporadic melanoma, a cancer originating from melanocytes. Evidence now suggests the involvement of NF1 mutations in melanoma resistance to targeted therapies. Although NF1 is ubiquitously expressed, genetic links between NF1 and genes involved in melanocyte biology have been described, implying the lineage-specific mechanisms. In this review, we summarize and discuss the latest advances related to the roles of NF1 in melanocyte biology and in cutaneous melanoma.

Keywords
NF1 cancer melanocyte melanoma neurofibromatosis type 1
MeSH 主题词
Animals Cell Lineage/genetics Humans Melanocytes/pathology Melanoma/genetics,pathology Mutation Neurofibromin 1/genetics Skin Neoplasms/genetics,pathology
化学物质
Neurofibromin 1
作者与单位
共 2 位作者,点击展开单位 / ORCID
Larribère Lionel
Skin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Germany. | Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Mannheim, Germany.
Utikal Jochen
Skin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Germany. | Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Mannheim, Germany.
Article Info
Journal
Pigment cell & melanoma research
Abbr.
Pigment Cell Melanoma Res
ISSN
1755-148X
Published
2016-00-00
页码
417-25
Language
English
Country/Region
England
NLM ID
101318927
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