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子宫内膜癌可能是 MUTYH 相关息肉病癌症谱的一部分

英文原题:Endometrial cancer may be part of the MUTYH-associated polyposis cancer spectrum.

查看英文原题

Endometrial cancer may be part of the MUTYH-associated polyposis cancer spectrum.

PubMed 2021/11/11(内容时间) Eur J Med Genet Q3 · IF 2.2(JCR 2025)

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中文摘要

MUTYH基因编码DNA糖基化酶,可防止G:C碱基对向T:A碱基对转换。携带双等位基因致病性生殖系MUTYH变异的患者会发生腺瘤性息肉病,称为MUTYH相关息肉病(MAP)。已有MAP患者发生子宫内膜癌的报道,但MUTYH功能缺失在致癌过程中的作用仍不明确。本文首次报告一例61岁MAP患者的子宫内膜癌病例,肿瘤中G:C向T:A转换明显增多。研究者通过二代测序获得关注的单核苷酸变异、肿瘤突变负荷(TMB)及体细胞突变谱,并评估TIL(肿瘤浸润淋巴细胞)水平和免疫浸润表型。患者子宫内膜癌TMB较高(31.5个变异/Mb),富集G:C向T:A转换,并存在KRAS驱动性致病变异c.34G>T,p.(Gly12Cys),提示MUTYH功能缺失可能参与肿瘤发生。MUTYH功能缺失可能参与MAP患者子宫内膜癌的发生。

展开英文摘要原文

The MUTYH gene encodes a DNA glycosylase that prevents G:C T:A transversions. Patients with biallelic pathogenic germline MUTYH variants develop an adenomatous polyposis called MUTYH-associated polyposis (MAP). Endometrial cancers have been reported in patients with MAP, but the role of MUTYH loss of function in the oncogenesis remains unclear.

We report for the first time a case of endometrial carcinoma with excess of G:C T:A transversions in a 61-year-old patient with MAP. Single nucleotide variants of interest, Tumor Mutational Burden (TMB) and somatic mutation profile were obtained from Next-Generation Sequencing (NGS). The Tumor-Infiltrating Lymphocyte (TIL) level and immune infiltrate phenotype were assessed.

The endometrial cancer had a high TMB (31. 5 variants/Mb) with enrichment in G:C T:A transversions and the presence of a driver pathogenic variant c. 34G>T, p. (Gly12Cys) in KRAS, suggesting a role of MUTYH loss of function in oncogenesis. MUTYH loss of function could be involved in endometrial cancer in patients with MAP.

论文信息

作者
Villy MC、Masliah-Planchon J、Buecher B、Beaulaton C、Vincent-Salomon A、Stoppa-Lyonnet D、Colas C
第一作者单位
Département de Génétique (Department of Genetics), Institut Curie, Paris, France.France
通讯作者单位
Département de Génétique (Department of Genetics), Institut Curie, Paris, France; Paris Sciences & Lettres Research University, Paris, France. Electronic address: chrystelle.colas@curie.fr.France
文献类型
病例报告
期刊
European journal of medical genetics2022 Jan
原文标识
PubMed 34775073 · DOI 10.1016/j.ejmg.2021.104385