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TERT 启动子突变与皮脂肿瘤。

TERT promoter mutation in sebaceous neoplasms.

机构信息

Department of Pathology, Medical School, Universidad Complutense, Instituto i+12, Hospital Universitario 12 de Octubre, CIBERONC, Madrid, Spain.

Department of Pathology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

出版信息

Virchows Arch. 2021 Sep;479(3):551-558. doi: 10.1007/s00428-021-03083-9. Epub 2021 Mar 25.

Abstract

TERT promoter (TERTp) mutations widely occur in multiple human neoplasms, and they have been related to different clinicopathological features. To date, this mutation has not been identified in sebaceous tumors. Here, we analyzed TERTp mutations in 91 sebaceous neoplasms (17 adenomas, 45 sebaceomas, and 29 carcinomas). We detected mutations in 26.7% (8 of 29) of sebaceous carcinomas by pyrosequencing and Sanger sequencing. No mutation was detected in adenomas or sebaceomas. The difference was significant between sebaceoma and carcinoma. The most frequent TERTp mutations were C228T and C250T in 37.5% (3 of 8) of mutated cases each one. The mutation was not associated with poor clinical evolution. Using NGS, 20 of 29 (68.5%) sebaceous carcinomas harbored mutations in 8 of the 30 genes analyzed (TP53, TERTp, EGFR, ATRX, PDGFRA, CDKN2A, PTEN, and ACVR1). With immunohistochemistry, only 1 of 8 (12.5%) TERTp-mutated carcinomas lacked mismatch repair (MMR) protein expression compared to 6 of 21 (31.6%) of non-mutated ones. Sebaceous carcinomas with MMR protein expression had significantly higher frequency of total mutations and TP53 and TERTp mutations than MMR protein-deficient carcinomas. In conclusion, TERTp mutation has been detected in sebaceous carcinomas, and its presence could be useful to differentiate sebaceous carcinoma from sebaceoma, a difficult histopathological challenge.

摘要

TERT 启动子(TERTp)突变广泛存在于多种人类肿瘤中,与不同的临床病理特征相关。迄今为止,这种突变尚未在皮脂肿瘤中被发现。在这里,我们分析了 91 例皮脂肿瘤(17 例腺瘤、45 例皮脂瘤和 29 例癌)的 TERTp 突变。通过焦磷酸测序和 Sanger 测序,我们在 29 例皮脂癌中检测到突变,占 26.7%(8/29)。在腺瘤或皮脂瘤中未检测到突变。这与腺瘤和癌之间的差异具有统计学意义。最常见的 TERTp 突变是 C228T 和 C250T,各占突变病例的 37.5%(3/8)。突变与不良临床转归无关。使用 NGS,在 29 例皮脂癌中,在分析的 30 个基因中的 8 个(TP53、TERTp、EGFR、ATRX、PDGFRA、CDKN2A、PTEN 和 ACVR1)中发现 20 例(68.5%)存在突变。通过免疫组化,与 21 例非突变病例(31.6%)相比,只有 1 例(12.5%) TERTp 突变型癌缺乏错配修复(MMR)蛋白表达。具有 MMR 蛋白表达的皮脂癌中总突变、TP53 和 TERTp 突变的频率明显高于 MMR 蛋白缺失的皮脂癌。总之,在皮脂癌中检测到 TERTp 突变,其存在有助于将皮脂癌与具有挑战性的组织病理学特征的皮脂瘤相区分。

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