Osteosarcoma, a highly aggressive bone cancer, poses significant treatment challenges. This study investigates a novel approach utilizing induced pluripotent stem cells (iPSCs) engineered with the FGFR3-TACC3 fusion gene to generate cytotoxic T lymphocytes (CTLs) targeting osteosarcoma. The aim was to assess the efficacy of iPSC-derived CTLs in combating osteosarcoma progression. Abnormal expression of the FGFR3-TACC3 fusion gene was confirmed in osteosarcoma samples. iPSCs were successfully modified to express the fusion gene and were then differentiated into CTLs. In vitro experiments demonstrated that these modified CTLs effectively killed osteosarcoma cells, induced apoptosis, and inhibited migration and invasion. Findings were validated in in vivo experiments. This study suggests that iPSC-derived CTLs targeting FGFR3-TACC3 hold promise for personalized immunotherapy against osteosarcoma.
Keyphrases
- induced apoptosis
- induced pluripotent stem cells
- copy number
- genome wide
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- poor prognosis
- genome wide identification
- dna methylation
- bone mineral density
- gene expression
- transcription factor
- postmenopausal women
- deep learning
- smoking cessation
- squamous cell
- combination therapy