Laboratory of Functional Genetics of Rare Diseases, Department of Microbiology and Genetics, University of Salamanca (USAL), 37007 Salamanca, Spain.
GIR of Biomedicine of Rare Diseases, University of Salamanca (USAL), 37007 Salamanca, Spain.
Int J Mol Sci. 2024 Aug 6;25(16):8563. doi: 10.3390/ijms25168563.
RASopathies are a group of related genetic disorders caused by mutations in genes within the RAS/MAPK signaling pathway. This pathway is crucial for cell division, growth, and differentiation, and its disruption can lead to a variety of developmental and health issues. RASopathies present diverse clinical features and pose significant diagnostic and therapeutic challenges. Studying the landscape of biomarkers in RASopathies has the potential to improve both clinical practices and the understanding of these disorders. This review provides an overview of recent discoveries in RASopathy molecular profiling, which extend beyond traditional gene mutation analysis. mRNAs, non-coding RNAs, protein expression patterns, and post-translational modifications characteristic of RASopathy patients within pivotal signaling pathways such as the RAS/MAPK, PI3K/AKT/mTOR, and Rho/ROCK/LIMK2/cofilin pathways are summarized. Additionally, the field of metabolomics holds potential for uncovering metabolic signatures associated with specific RASopathies, which are crucial for developing precision medicine. Beyond molecular markers, we also examine the role of histological characteristics and non-invasive physiological assessments in identifying potential biomarkers, as they provide evidence of the disease's effects on various systems. Here, we synthesize key findings and illuminate promising avenues for future research in RASopathy biomarker discovery, underscoring rigorous validation and clinical translation.
RAS 病是一组与 RAS/MAPK 信号通路中基因突变相关的遗传疾病。该通路对细胞分裂、生长和分化至关重要,其功能障碍可导致多种发育和健康问题。RAS 病表现出多样化的临床特征,对诊断和治疗构成重大挑战。研究 RAS 病中的生物标志物图谱有可能改善临床实践和对这些疾病的理解。本综述概述了 RAS 病分子谱分析方面的最新发现,这些发现超出了传统的基因突变分析。总结了 RAS/MAPK、PI3K/AKT/mTOR 和 Rho/ROCK/LIMK2/cofilin 等关键信号通路中 RAS 病患者的 mRNA、非编码 RNA、蛋白质表达模式和翻译后修饰特征。此外,代谢组学领域有可能发现与特定 RAS 病相关的代谢特征,这对于开发精准医学至关重要。除了分子标志物,我们还研究了组织学特征和非侵入性生理评估在识别潜在生物标志物方面的作用,因为它们提供了疾病对各种系统影响的证据。在这里,我们综合了关键发现,并阐明了 RAS 病生物标志物发现的未来研究有前景的途径,强调了严格的验证和临床转化。