TY - JOUR
T1 - Nonoverlapping Clinical and Mutational Patterns in Melanomas from the Female Genital Tract and Atypical Genital Nevi
AU - Yélamos, Oriol
AU - Merkel, Emily A.
AU - Sholl, Lauren Meldi
AU - Zhang, Bin
AU - Amin, Sapna M.
AU - Lee, Christina Y.
AU - Guitart, Gerta E.
AU - Yang, Jingyi
AU - Wenzel, Alexander T.
AU - Bunick, Christopher G.
AU - Yazdan, Pedram
AU - Choi, Jaehyuk
AU - Gerami, Pedram
N1 - Funding Information:
This study was performed with support from the IDP Foundation. PG has served as a consultant to Myriad Genomics, DermTech International, and Castle Biosciences and has received honoraria for this.
Publisher Copyright:
© 2016 The Authors
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Genital melanomas (GM) are the second most common cancer of the female external genitalia and may be confused with atypical genital nevi (AGN), which exhibit atypical histological features but have benign behavior. In this study, we compared the clinical, histological, and molecular features of 19 GM and 25 AGN. We described chromosomal copy number aberrations and the mutational status of 50 oncogenes and tumor suppressor genes in both groups. Our study showed that a pigmented lesion occurring in mucosal tissue, particularly in postmenopausal women, was more likely to be a melanoma than a nevus. GM had high levels of chromosomal instability, with many copy number aberrations. Furthermore, we found a completely nonoverlapping pattern of oncogenic mutations when comparing GM and AGN. In GM, we report somatic mutations in KIT and TP53. Conversely, AGN had frequent BRAF V600E mutations, which were not seen in any of the GM. Our results show that GM and AGN have distinct clinical and molecular changes and that GM have a different mutational pattern compared with AGN.
AB - Genital melanomas (GM) are the second most common cancer of the female external genitalia and may be confused with atypical genital nevi (AGN), which exhibit atypical histological features but have benign behavior. In this study, we compared the clinical, histological, and molecular features of 19 GM and 25 AGN. We described chromosomal copy number aberrations and the mutational status of 50 oncogenes and tumor suppressor genes in both groups. Our study showed that a pigmented lesion occurring in mucosal tissue, particularly in postmenopausal women, was more likely to be a melanoma than a nevus. GM had high levels of chromosomal instability, with many copy number aberrations. Furthermore, we found a completely nonoverlapping pattern of oncogenic mutations when comparing GM and AGN. In GM, we report somatic mutations in KIT and TP53. Conversely, AGN had frequent BRAF V600E mutations, which were not seen in any of the GM. Our results show that GM and AGN have distinct clinical and molecular changes and that GM have a different mutational pattern compared with AGN.
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U2 - 10.1016/j.jid.2016.05.094
DO - 10.1016/j.jid.2016.05.094
M3 - Article
C2 - 27220476
AN - SCOPUS:84992520774
SN - 0022-202X
VL - 136
SP - 1858
EP - 1865
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 9
ER -