Functional & Integrative Genomics, Год журнала: 2025, Номер 25(1)
Опубликована: Март 25, 2025
Язык: Английский
Functional & Integrative Genomics, Год журнала: 2025, Номер 25(1)
Опубликована: Март 25, 2025
Язык: Английский
Journal of Clinical Oncology, Год журнала: 2025, Номер unknown
Опубликована: Янв. 13, 2025
Colorectal cancer (CRC) remains a major global health burden, being one of the most prevalent cancers with high mortality rates. Despite advances in conventional treatment modalities, patients metastatic CRC often face limited options and poor outcomes. Chimeric antigen receptor-T (CAR-T) cell therapy, initially successful hematologic malignancies, presents promising avenue for treating solid tumors, including CRC. This review explores potential CAR-T therapy by analyzing clinical trials highlighting prominent CRC-specific targets. We discuss challenges such as immunosuppressive microenvironment, tumor heterogeneity, physical barriers that limit efficacy. Emerging strategies, logic-gated dual-targeting cells, offer practical solutions to overcome these hurdles. Furthermore, we explore combination immune checkpoint inhibitors enhance T-cell persistence infiltration. As field continues evolve, therapies hold significant revolutionizing landscape
Язык: Английский
Процитировано
0Pharmacological Research, Год журнала: 2025, Номер 212, С. 107637 - 107637
Опубликована: Янв. 29, 2025
Gastric cancer remains a significant global health burden, characterized by regional variations in incidence and poor survival prospects advanced stages. Natural killer (NK) cells play crucial role the body's anti-cancer defense, chimeric antigen receptor (CAR)-NK cell therapy is gaining attention as cutting-edge promising treatment method. This study aims to tackle challenge of TGF-β-mediated tumor immune evasion within immunosuppressive microenvironment designing novel cytokine TRII/21R, which consists extracellular domains TGF-β II (TRII) transmembrane intracellular IL-21 (21R) can convert signal from (TME) into an NK activation through IL-21R-STAT3 pathway. We successfully constructed NKG2D-CAR-NK expressing TRII/21R demonstrated strong anti-tumor activity against both vitro vivo. The co-expression CAR-NK enhanced cytotoxicity, promoted proliferation capabilities, reduced expression exhaustion markers. In xenograft mouse model, TRII/21R-CAR-NK significantly inhibited growth improved rate tumor-bearing mice compared receiving control cells. Additionally, cells' infiltration, activation, persistence tumor, indicating robust response mediated JAK-STAT3 signaling underscores therapeutic potential TRII/21R-modified breakthrough strategy for combating cancer.
Язык: Английский
Процитировано
0Nano Biomedicine and Engineering, Год журнала: 2025, Номер unknown
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Functional & Integrative Genomics, Год журнала: 2025, Номер 25(1)
Опубликована: Март 25, 2025
Язык: Английский
Процитировано
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