| Autor: |
Nance RL; Scott-Ritchey Research Center, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA.; Department of Pathobiology, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA., Wang X; Scott-Ritchey Research Center, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA.; Department of Pathobiology, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA., Sandey M; Department of Pathobiology, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA., Matz BM; Department of Clinical Sciences, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA., Thomas A; Department of Nursing, Tuskegee University, Tuskegee, AL 36088, USA., Smith BF; Scott-Ritchey Research Center, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA.; Department of Pathobiology, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA. |
| Abstrakt: |
Osteosarcoma (OSA) is a highly aggressive bone tumor primarily affecting pediatric or adolescent humans and large-breed dogs. Canine OSA shares striking similarities with its human counterpart, making it an invaluable translational model for uncovering the disease's complexities and developing novel therapeutic strategies. Tumor heterogeneity, a hallmark of OSA, poses significant challenges to effective treatment due to the evolution of diverse cell populations that influence tumor growth, metastasis, and resistance to therapies. In this study, we apply single-nuclei multiome sequencing, encompassing ATAC (Assay for Transposase-Accessible Chromatin) and GEX (Gene Expression, or RNA) sequencing, to a treatment-naïve primary canine osteosarcoma. This comprehensive approach reveals the complexity of the tumor microenvironment by simultaneously capturing the transcriptomic and epigenomic profiles within the same nucleus. Furthermore, these results are analyzed in conjunction with bulk RNA sequencing and differential analysis of the same tumor and patient-matched normal bone. By delving into the intricacies of OSA at this unprecedented level of detail, we aim to unravel the underlying mechanisms driving intra-tumoral heterogeneity, opening new avenues for therapeutic interventions in both human and canine patients. This study pioneers an approach that is broadly applicable, while demonstrating significant heterogeneity in the context of a single individual's tumor. |
