Kocikowski Mikolaj, Yébenes Mayordomo Marcos, Alfaro Javier, Parys Maciej
International Centre for Cancer Vaccine Science, University of Gdansk, Gdansk, Poland.
The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh.
PLoS Comput Biol. 2025 Aug 11;21(8):e1013270. doi: 10.1371/journal.pcbi.1013270. eCollection 2025 Aug.
In the quest for improved therapeutics targeting immune checkpoints (ICs), we turn to spontaneously developing dog (canine) cancers, some of which genetically and clinically mirror the human counterparts. Despite its potential, canine cancer immunology remains largely unexplored. Here, we examine the RNA-seq-based expression of 44 ICs across 14 canine cancer types and an extensive human dataset. We unveil diverse canine IC expression patterns and unique human IC signatures that reflect the histological type and primary site of cancer. We uncover a striking similarity between canine brain cancers, osteosarcoma, and their human counterparts, identifying them as prospective immunotherapy models. Four ICs - CD160, A2AR, NKG2A, and OX40 - are key to the differences observed between species. We also find that individual human IC signatures vary in how well they align with their respective cancer types, a pattern that may influence future approaches to personalized therapy. This exploration highlights aspects of canine and human cancer immunology that warrant further study, setting the stage for discoveries at their crossroads.
在寻求针对免疫检查点(ICs)的改进疗法的过程中,我们将目光转向自发形成的犬类癌症,其中一些在基因和临床方面与人类癌症相似。尽管具有潜力,但犬类癌症免疫学在很大程度上仍未得到充分探索。在此,我们研究了14种犬类癌症类型以及大量人类数据集基于RNA测序的44种ICs的表达情况。我们揭示了反映癌症组织学类型和原发部位的多样犬类IC表达模式和独特人类IC特征。我们发现犬类脑癌、骨肉瘤与其人类对应癌症之间存在惊人的相似性,将它们确定为潜在的免疫治疗模型。四种ICs——CD160、A2AR、NKG2A和OX40——是观察到的物种间差异的关键。我们还发现,个体人类IC特征与其各自癌症类型的匹配程度各不相同,这种模式可能会影响未来个性化治疗的方法。这一探索突出了犬类和人类癌症免疫学中值得进一步研究的方面,为在它们的交叉点上的发现奠定了基础。