Al Jarroudi Ouissam, El Bairi Khalid, Brahmi Sami Aziz, Afqir Said
Department of Medical Oncology, Mohammed VI University Hospital, Oujda, Morocco.
Faculty of Medicine and Pharmacy, Mohamed I University, Oujda, Morocco.
Front Oncol. 2025 Aug 20;15:1418537. doi: 10.3389/fonc.2025.1418537. eCollection 2025.
Non-Gastrointestinal Stromal Tumors (Non-GIST) Soft Tissue Sarcomas (STS) are highly aggressive and challenging diseases with poor prognosis and limited therapeutic options. Molecular profiling is urgently required to gain a deeper understanding of STS pathogenesis and to identify a comprehensive landscape of genomic alterations in order to develop effective targeted therapies. The mitogen-activated protein kinase (MAPK) signaling pathway is a key molecular mechanism involved in sarcoma development. This study aims to conduct a literature review on the involvement of the MAPK cascade in non-GIST STS, with a focus on the role of MAPK inhibitors in the current treatment paradigm for STS. Furthermore, recent data have provided promising preliminary findings regarding the use of new molecular agents targeting the MAPK pathway, either as single therapies or in combination with other drugs. Numerous clinical trials are currently ongoing, and their outcomes are eagerly awaited. Further research is required in both translational and clinical settings to molecularly characterize STS, identify novel causal alterations, accelerate target discovery, and identify potential biomarkers. Moreover, the development of novel nanomaterials provides a promising perspective that may lead to significant advancements in clinical practice.
非胃肠道间质瘤(Non-GIST)软组织肉瘤(STS)是极具侵袭性且具有挑战性的疾病,预后较差,治疗选择有限。迫切需要进行分子谱分析,以更深入地了解STS的发病机制,并识别基因组改变的全面情况,从而开发有效的靶向治疗方法。丝裂原活化蛋白激酶(MAPK)信号通路是参与肉瘤发展的关键分子机制。本研究旨在对MAPK级联在非GIST STS中的作用进行文献综述,重点关注MAPK抑制剂在当前STS治疗模式中的作用。此外,最近的数据提供了关于使用靶向MAPK途径的新型分子药物的有前景的初步发现,这些药物既可以作为单一疗法,也可以与其他药物联合使用。目前正在进行大量临床试验,人们急切期待其结果。在转化和临床环境中都需要进一步研究,以对STS进行分子特征分析、识别新的因果改变、加速靶点发现并确定潜在的生物标志物。此外,新型纳米材料的开发提供了一个有前景的前景,可能会在临床实践中带来重大进展。