PTEN Methylation Dependent Sinonasal Mucosal Melanoma

被引:4
|
作者
Lee, Sang Hee [1 ]
Roh, Mi Ryung [1 ]
Kang, Beodeul [2 ,3 ]
Park, Kyu Hyun [2 ,3 ]
Kim, Soo Hee [4 ]
Lee, Sang Eun [1 ]
Rha, Sun Young [2 ,3 ,5 ]
机构
[1] Yonsei Univ, Coll Med, Dept Dermatol, Severance Hosp,Cutaneous Biol Res Inst, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Yonsei Song Dang Inst Canc Res, Seoul, South Korea
[3] Yonsei Univ, Coll Med, Dept Internal Med, Div Med Oncol, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Dept Pathol, Seoul, South Korea
[5] Yonsei Univ, Coll Med, Brain Korea Plus Project Med Sci 21, Seoul, South Korea
来源
CANCER RESEARCH AND TREATMENT | 2016年 / 48卷 / 02期
基金
新加坡国家研究基金会;
关键词
Methylation; Phosphatase and tensin homolog; Sinonasal melanoma; MUTATIONS; GENE; EXPRESSION; BRAF; NRAS;
D O I
10.4143/crt.2014.356
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sinonasal mucosal melanoma (SMM) is an aggressive and rare type of melanoma. Although the classic RAS-RAF-MEK pathway is thought to be the main pathway involved in melanoma pathogenesis, genetic alterations in the phosphatidylinositol 3-kinase-AKT pathway, including PTEN-regulated signaling, are also thought to contribute. So far, data regarding altered PTEN expression and epigenetic mechanism of PTEN silencing in development of SMM is extremely limited. Herein we report on a case of SMM with liver and bone metastases with an epigenetic alteration of PTEN. Results of mutation analysis for BRAF, NRAS, HRAS, KRAS, PIK3CA, c-Kit, and PTEN were negative; however, methylation of PTEN CpG islands was observed. Our case not only supports PTEN as a major tumor suppressor involved in melanoma tumorigenesis, but also a potential epigenetic mechanism of PTEN silencing in development of SMM.
引用
收藏
页码:853 / 858
页数:6
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