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NRAS 突变型皮肤黑色素瘤中 p16(INK4A)启动子甲基化的高频性。

High frequency of p16(INK4A) promoter methylation in NRAS-mutated cutaneous melanoma.

机构信息

Department of Oncology and Pathology, Cancer Center Karolinska, Karolinska Institutet/Karolinska University Hospital, Stockholm, Sweden.

出版信息

J Invest Dermatol. 2010 Dec;130(12):2809-17. doi: 10.1038/jid.2010.216. Epub 2010 Aug 12.

Abstract

The p16(INK4A) tumor suppressor is often deleted, or otherwise inactivated, in malignant melanoma. To investigate the loss of p16(INK4A) in greater detail, we analyzed 77 cutaneous melanoma metastases. Of these 56 retained at least one p16(INK4A) allele, and 21 had biallelic deletions. Using methylation-specific PCR, direct sequencing, and immunohistochemical methods, we analyzed p16(INK4A) promoter methylation, mutations, and protein expression, respectively. In addition, 14 corresponding primary tumors were analyzed for protein expression. Results were compared to clinicopathological parameters and previously obtained data regarding mutations in proto-oncogenes NRAS and BRAF. Results revealed that p16(INK4A) promoter methylation was present in 15 of 59 (25%) metastases; nonsynonymous mutations in 9 of 56 (16%) metastases; and protein expression in 12 of 67 (18%) metastases. Protein expression was lost during progression from primary to metastatic tumors, 71% (10 of 14) and 43% (6 of 14) being positive, respectively. However, the genetic and epigenetic alterations of p16(INK4A) observed could not explain the lack of p16(INK4A) protein in 27 metastases, indicating the presence of additional inactivating mechanisms for p16(INK4A). Interestingly, p16(INK4A) promoter methylation was significantly overrepresented in NRAS-mutated samples compared to NRAS wild-type samples (P=0.0004), indicating an association between these two events.

摘要

p16(INK4A)肿瘤抑制因子在恶性黑色素瘤中经常缺失或失活。为了更详细地研究 p16(INK4A)的缺失,我们分析了 77 例皮肤黑色素瘤转移灶。其中 56 例保留了至少一个 p16(INK4A)等位基因,21 例存在等位基因双缺失。我们分别采用甲基化特异性 PCR、直接测序和免疫组化方法分析 p16(INK4A)启动子甲基化、突变和蛋白表达。此外,还对 14 例相应的原发性肿瘤进行了蛋白表达分析。将结果与临床病理参数以及先前获得的关于原癌基因 NRAS 和 BRAF 突变的数据进行比较。结果显示,在 59 例转移灶中(25%)存在 p16(INK4A)启动子甲基化;在 56 例转移灶中有 9 例(16%)存在非编码突变;在 67 例转移灶中有 12 例(18%)存在蛋白表达。p16(INK4A)蛋白在原发性肿瘤向转移性肿瘤进展过程中丢失,分别有 71%(10/14)和 43%(6/14)的样本为阳性。然而,在 27 例转移灶中观察到的 p16(INK4A)的遗传和表观遗传改变并不能解释 p16(INK4A)蛋白的缺失,表明 p16(INK4A)存在其他失活机制。有趣的是,与 NRAS 野生型样本相比,NRAS 突变样本中 p16(INK4A)启动子甲基化显著增加(P=0.0004),表明这两个事件之间存在关联。

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