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李-佛美尼综合征异质性。

Li-Fraumeni syndrome heterogeneity.

机构信息

Pediatric Oncology, La Fe Hospital, Av. Fernando Abril Martorell 106, 46026, Valencia, Spain.

Clinical and Translational Oncology Research Group, La Fe Hospital, Valencia, Spain.

出版信息

Clin Transl Oncol. 2020 Jul;22(7):978-988. doi: 10.1007/s12094-019-02236-2. Epub 2019 Nov 5.

Abstract

Clinical variability is commonly seen in Li-Fraumeni syndrome. Phenotypic heterogeneity is present among different families affected by the same pathogenic variant in TP53 gene and among members of the same family. However, causes of this huge clinical spectrum have not been studied in depth. TP53 type mutation, polymorphic variants in TP53 gene or in TP53-related genes, copy number variations in particular regions, and/or epigenetic deregulation of TP53 expression might be responsible for clinical heterogeneity. In this review, recent advances in the understanding of genetic and epigenetic aspects influencing Li-Fraumeni phenotype are discussed.

摘要

临床变异性在 Li-Fraumeni 综合征中很常见。同一 TP53 基因突变影响的不同家族以及同一家庭的成员之间存在表型异质性。然而,尚未深入研究导致这种巨大临床谱的原因。TP53 型突变、TP53 基因或与 TP53 相关基因中的多态性变异、特定区域的拷贝数变异,以及/或 TP53 表达的表观遗传失调可能是导致临床异质性的原因。本文讨论了对影响 Li-Fraumeni 表型的遗传和表观遗传因素的最新认识。

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