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TP53和TERT启动子突变在甲状腺髓样癌中的次要作用:新病例报告及文献综述

Minor role of TP53 and TERT promoter mutations in medullary thyroid carcinoma: report of new cases and revision of the literature.

作者信息

Casalini Roberta, Romei Cristina, Ciampi Raffaele, Ramone Teresa, Prete Alessandro, Gambale Carla, Matrone Antonio, Torregrossa Liborio, Ugolini Clara, Elisei Rossella

机构信息

Department of Clinical and Experimental Medicine, Unit of Endocrinology, University Hospital of Pisa, Pisa, Italy.

Department of Surgical, Medical, Molecular Pathology and Critical Area, Unit of Pathology, University Hospital of Pisa, Pisa, Italy.

出版信息

Endocrine. 2025 Jan;87(1):243-251. doi: 10.1007/s12020-024-03990-2. Epub 2024 Aug 23.

Abstract

PURPOSE

Aims of this study were to investigate the prevalence of TP53 and TERT mutations in Medullary Thyroid carcinoma (MTC) and their role in inducing aggressiveness in positive cases.

METHODS

We performed a literature search in PubMed to identify studies investigating the prevalence of TERT and TP53 mutations in MTC. We also included data on MTC cases (n = 193) obtained at our center and unpublished. The in-silico pathogenicity of the TP53 mutations has been evaluated by predictor tools.

RESULTS

We identified a total of 25 and 11 published papers: all together 1280 cases have been investigated for the presence of TP53 mutations and 974 for TERT promoter mutation. Twenty-five out of 1280 (2%) cases had a TP53 mutation while only 3/974 MTC cases (0.3%) have been found to be positive for TERT promoter mutations. Among all, we identified 19 different TP53 mutations that in 12 cases were demonstrated to have an in silico predicted high pathogenic role and a high impact on protein function. Three non-sense and 4 probably not damaging mutations were also reported. The pathogenic role of the TERT promoter mutations has been previously in vitro determined. No correlation between TP53 and/or TERT mutations and aggressiveness of MTC has been demonstrated.

CONCLUSION

The prevalence of TP53 and TERT promoter mutations is very low in MTC. The reported mutations are pathogenic in the majority of cases. Because of their rarity it is not possible to clarify if they play or not a role in the pathogenesis and/or aggressiveness of this specific thyroid tumor.

摘要

目的

本研究旨在调查甲状腺髓样癌(MTC)中TP53和TERT突变的发生率及其在阳性病例中诱导侵袭性的作用。

方法

我们在PubMed上进行了文献检索,以确定研究MTC中TERT和TP53突变发生率的研究。我们还纳入了在我们中心获得的193例MTC病例的数据且未发表。通过预测工具评估了TP53突变的计算机模拟致病性。

结果

我们共鉴定出25篇和11篇已发表的论文:总共对1280例病例进行了TP53突变检测,对974例病例进行了TERT启动子突变检测。1280例病例中有25例(2%)发生TP53突变,而974例MTC病例中仅3例(0.3%)TERT启动子突变呈阳性。在所有病例中,我们鉴定出19种不同的TP53突变,其中12例在计算机模拟中被证明具有高致病性作用且对蛋白质功能有高影响。还报告了3种无义突变和4种可能无损害的突变。TERT启动子突变的致病作用先前已在体外确定。未证明TP53和/或TERT突变与MTC的侵袭性之间存在相关性。

结论

MTC中TP53和TERT启动子突变的发生率非常低。报告的突变在大多数情况下具有致病性。由于它们罕见,无法阐明它们是否在这种特定甲状腺肿瘤的发病机制和/或侵袭性中起作用。

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