Fortes-Andrade Tânia, Almeida Jani Sofia, Sousa Luana Madalena, Santos-Rosa Manuel, Freitas-Tavares Paulo, Casanova José Manuel, Rodrigues-Santos Paulo
Center for Neuroscience and Cell Biology (CNC), Laboratory of Immunology and Oncology, University of Coimbra, 3004-504 Coimbra, Portugal.
Faculty of Medicine, Immunology Institute, University of Coimbra, 3004-504 Coimbra, Portugal.
Cancers (Basel). 2021 Jul 31;13(15):3865. doi: 10.3390/cancers13153865.
Soft-tissue sarcomas (STS) represent about 80% of sarcomas, and are a heterogeneous group of rare and malignant tumors. STS arise from mesenchymal tissues and can grow into structures such as adipose tissue, muscles, nervous tissue and blood vessels. Morphological evaluation has been the standard model for the diagnosis of sarcomas, and even in samples with similar characteristics, they present a diversity in cytogenetic and genetic sequence alterations, which further increases the diversity of sarcomas. This variety is one of the main challenges for the classification and understanding of STS patterns, as well as for their respective treatments, which further decreases patient survival (<5 years). Despite some studies, little is known about the immunological profile of STS. As for the immunological profile of STS in relation to NK cells, there is also a shortage of studies. Observations made in solid tumors show that the infiltration of NK cells in tumors is associated with a good prognosis of the disease. Notwithstanding the scarcity of studies to characterize NK cells, their receptors, and ligands in STS, it is noteworthy that the progression of these malignancies is associated with altered NK phenotypes. Despite the scarcity of information on the function of NK cells, their phenotypes and their regulatory pathways in STS, the findings of this study support the additional need to explore NK cell-based immunotherapy in STS further. Some clinical trials, very tentatively, are already underway. STS clinical trials are still the basis for adoptive NK-cell and cytokine-based therapy.
软组织肉瘤(STS)约占肉瘤的80%,是一组异质性的罕见恶性肿瘤。STS起源于间充质组织,可生长到脂肪组织、肌肉、神经组织和血管等结构中。形态学评估一直是肉瘤诊断的标准模式,即使在具有相似特征的样本中,它们在细胞遗传学和基因序列改变方面也存在差异,这进一步增加了肉瘤的多样性。这种多样性是分类和理解STS模式及其各自治疗方法的主要挑战之一,这也进一步降低了患者的生存率(<5年)。尽管有一些研究,但对STS的免疫特征了解甚少。至于STS与自然杀伤细胞(NK细胞)相关的免疫特征,研究也很缺乏。在实体瘤中的观察表明,肿瘤中NK细胞的浸润与疾病的良好预后相关。尽管在STS中表征NK细胞、其受体和配体的研究很少,但值得注意的是,这些恶性肿瘤的进展与NK细胞表型的改变有关。尽管关于STS中NK细胞的功能、其表型及其调节途径的信息很少,但本研究结果支持进一步探索基于NK细胞的免疫疗法在STS中的应用。一些非常初步的临床试验已经在进行中。STS临床试验仍然是过继性NK细胞和基于细胞因子疗法的基础。