Medical Oncology Department, Centro Hospitalar Universitário Lisboa Norte, 1649-028 Lisboa, Portugal.
Vascular Biology & Cancer Microenvironment Lab, Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina da Universidade de Lisboa, 1649-028 Lisboa, Portugal.
Int J Mol Sci. 2022 Sep 28;23(19):11430. doi: 10.3390/ijms231911430.
Soft tissue sarcomas (STS) prognosis is disappointing, with current treatment strategies being based on a "fit for all" principle and not taking distinct sarcoma subtypes specificities and genetic/metabolic differences into consideration. The paucity of precision therapies in STS reflects the shortage of studies that seek to decipher the sarcomagenesis mechanisms. There is an urge to improve STS diagnosis precision, refine STS classification criteria, and increase the capability of identifying STS prognostic biomarkers. Single-omics and multi-omics studies may play a key role on decodifying sarcomagenesis. Metabolomics provides a singular insight, either as a single-omics approach or as part of a multi-omics strategy, into the metabolic adaptations that support sarcomagenesis. Although STS metabolome is scarcely characterized, untargeted and targeted metabolomics approaches employing different data acquisition methods such as mass spectrometry (MS), MS imaging, and nuclear magnetic resonance (NMR) spectroscopy provided important information, warranting further studies. New chromatographic, MS, NMR-based, and flow cytometry-based methods will offer opportunities to therapeutically target metabolic pathways and to monitorize the response to such metabolic targeting therapies. Here we provide a comprehensive review of STS omics applications, comprising a detailed analysis of studies focused on the metabolic landscape of these tumors.
软组织肉瘤(STS)的预后令人失望,目前的治疗策略基于“一刀切”的原则,没有考虑到不同的肉瘤亚型的特异性和遗传/代谢差异。STS 缺乏精准治疗反映了缺乏旨在破译肉瘤发生机制的研究。迫切需要提高 STS 的诊断精度,细化 STS 的分类标准,并提高识别 STS 预后生物标志物的能力。单组学和多组学研究可能在解码肉瘤发生方面发挥关键作用。代谢组学提供了一种独特的见解,无论是作为一种单组学方法还是作为多组学策略的一部分,都可以深入了解支持肉瘤发生的代谢适应。尽管 STS 的代谢组学尚未得到充分描述,但采用不同数据采集方法的靶向和非靶向代谢组学方法,如质谱(MS)、MS 成像和核磁共振(NMR)光谱学,提供了重要信息,值得进一步研究。新的色谱、MS、基于 NMR 的和基于流式细胞术的方法将为靶向代谢途径提供机会,并监测对这种代谢靶向治疗的反应。在这里,我们全面回顾了 STS 的组学应用,包括对这些肿瘤代谢景观的研究进行详细分析。