دورية أكاديمية

The synergy of 177Lu-FAPI-46 with tyrosine kinase inhibitor in a sarcoma patient-derived xenograft mouse model

التفاصيل البيبلوغرافية
العنوان: The synergy of 177Lu-FAPI-46 with tyrosine kinase inhibitor in a sarcoma patient-derived xenograft mouse model
المؤلفون: Jing-Ren Tseng, Cheng-Lung Hsu, Hsin-Hua Hsieh, Kung-Chu Ho, Yi-Hsiu Chung, Chun-Yi Wu
المصدر: Biomedical Journal, Vol 47, Iss 3, Pp 100744- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine (General)
LCC:Biology (General)
مصطلحات موضوعية: Sarcoma, Patient-derived xenograft (PDX), Fibroblast activation protein (FAP), 177Lu-FAPI-46, Medicine (General), R5-920, Biology (General), QH301-705.5
الوصف: Background: Given the heterogeneity and high mortality associated with metastatic soft tissue sarcoma, this study aims to evaluate the therapeutic efficacy of combining 177Lu-FAPI-46 with Pazopanib against this malignancy. Methods: Patient-derived xenograft (PDX)-bearing mice were randomly divided into three groups: the control group, the 177Lu-FAPI-46 monotherapy group, and the 177Lu-FAPI-46 combined with Pazopanib therapy group. Therapeutic efficacy was regularly monitored. Results: The microPET imaging showed a 0.84-fold decrease in the T/M ratio of 68Ga-FAPI-46 on day 7/8 post combination therapy, while the control group exhibited a 1.23-fold increase. Combination therapy significantly inhibited tumor proliferation, as evidenced by reduced Ki-67 and increased caspase 3 expressions. Notably, there was no significant body weight loss observed in any group. Conclusion: This study successfully demonstrated the reduction in FAP expression and suppression of tumor volume in sarcoma PDX following the combination therapy of 177Lu-FAPI-46 with Pazopanib.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2319-4170
Relation: http://www.sciencedirect.com/science/article/pii/S2319417024000477; https://doaj.org/toc/2319-4170
DOI: 10.1016/j.bj.2024.100744
URL الوصول: https://doaj.org/article/f83c372728994ea3895513cc77e1168e
رقم الأكسشن: edsdoj.f83c372728994ea3895513cc77e1168e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23194170
DOI:10.1016/j.bj.2024.100744