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PTEN 甲基化依赖型鼻腔鼻窦黏膜黑色素瘤。

PTEN Methylation Dependent Sinonasal Mucosal Melanoma.

机构信息

Department of Dermatology, Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Yonsei Song-Dang Institute for Cancer Research, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Cancer Res Treat. 2016 Apr;48(2):853-8. doi: 10.4143/crt.2014.356. Epub 2015 Mar 18.

Abstract

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.

摘要

鼻腔鼻窦黏膜黑色素瘤(SMM)是一种侵袭性和罕见的黑色素瘤。虽然经典的 RAS-RAF-MEK 通路被认为是黑色素瘤发病机制中的主要通路,但磷酸肌醇 3-激酶-AKT 通路中的遗传改变,包括 PTEN 调节的信号通路,也被认为与之相关。到目前为止,关于 SMM 发展过程中 PTEN 表达改变和 PTEN 沉默的表观遗传机制的数据极其有限。本文报告了一例伴有肝和骨转移的 SMM 病例,其存在 PTEN 的表观遗传改变。BRAF、NRAS、HRAS、KRAS、PIK3CA、c-Kit 和 PTEN 的突变分析结果均为阴性;然而,观察到了 PTEN CpG 岛的甲基化。本病例不仅支持 PTEN 作为参与黑色素瘤肿瘤发生的主要肿瘤抑制因子,还支持 SMM 发展过程中 PTEN 沉默的潜在表观遗传机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e805/4843734/381449920fb5/crt-2014-356f1.jpg

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