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丝裂原活化蛋白激酶途径激活(RAS病)及部分生长激素不敏感

Activation of the MAPK pathway (RASopathies) and partial growth hormone insensitivity.

作者信息

Malaquias Alexsandra C, Jorge Alexander A L

机构信息

Unidade de Endocrinologia Genética, Laboratório de Endocrinologia Celular e Molecular LIM25, Disciplina de Endocrinologia da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil; Unidade de Endocrinologia Pediátrica, Departamento de Pediatria, Irmandade da Santa Casa de Misericórdia de São Paulo, Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, Brazil.

Unidade de Endocrinologia Genética, Laboratório de Endocrinologia Celular e Molecular LIM25, Disciplina de Endocrinologia da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

出版信息

Mol Cell Endocrinol. 2021 Jan 1;519:111040. doi: 10.1016/j.mce.2020.111040. Epub 2020 Oct 1.

Abstract

RASopathies are a heterogeneous group of syndromes caused by germline mutations in genes encoding components of the RAS/MAPK pathway. Postnatal short stature is a cardinal feature of the RASopathies. Although the pathophysiology of these conditions is not fully understood to date, growth hormone insensitivity is one possibility, based on the observation of low IGF-1 values, generally preserved GH secretion and suboptimal growth response to recombinant human GH therapy. In this review, we will discuss the clinical and experimental evidence of GH insensitivity in patients with Noonan syndrome and other RASopathies, as well as their molecular basis.

摘要

RAS病是一组由编码RAS/丝裂原活化蛋白激酶(MAPK)信号通路组分的基因种系突变引起的综合征。出生后身材矮小是RAS病的主要特征。尽管目前对这些病症的病理生理学尚未完全了解,但基于胰岛素样生长因子-1(IGF-1)值低、生长激素(GH)分泌通常保留以及对重组人生长激素治疗的生长反应欠佳的观察结果,生长激素不敏感是一种可能的原因。在本综述中,我们将讨论努南综合征和其他RAS病患者生长激素不敏感的临床和实验证据及其分子基础。

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