CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Expand available targets for CAR-T therapy to overcome tumor drug resistance based on the "Evolutionary Traps".
Expand available targets for CAR-T therapy to overcome tumor drug resistance based on the "Evolutionary Traps".
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根据“进化陷阱”概念,靶向肿瘤耐药过程中获得的生存必需基因,可有效清除耐药细胞,但这一策略仍面临局限。本研究使用拉帕替尼耐药细胞检验“进化陷阱”概念;由于所识别基因缺乏可用药物,没有发现合适靶点。然而,研究发现膜蛋白 PDPN 在正常组织中低表达或不表达,却在拉帕替尼耐药肿瘤细胞中高表达。研究人员构建了 PDPN CAR-T 细胞,其在体内外均对拉帕替尼耐药肿瘤细胞表现出较强细胞毒性,提示 CAR-T 可能是基于“进化陷阱”克服肿瘤耐药的可行途径。为检验这一概念是否依赖特定细胞系或药物,研究人员分析了 21 种耐药肿瘤细胞的表达谱,发现 JAG1、GPC3 和 L1CAM 等适用于 CAR-T 治疗的靶点,在多种耐药肿瘤细胞中显著上调。本研究结果显示利用 CAR-T 治疗耐药肿瘤具有可行性,并拓展了“进化陷阱”概念。
Based on the concept of "Evolutionary Traps", targeting survival essential genes obtained during tumor drug resistance can effectively eliminate resistant cells. While, it still faces limitations. In this study, lapatinib-resistant cells were used to test the concept of "Evolutionary Traps" and no suitable target stand out because of the identified genes without accessible drug.
However, a membrane protein PDPN, which is low or non-expressed in normal tissues, is identified as highly expressed in lapatinib-resistant tumor cells. PDPN CAR-T cells were developed and showed high cytotoxicity against lapatinib-resistant tumor cells in vitro and in vivo, suggesting that CAR-T may be a feasible route for overcoming drug resistance of tumor based on "Evolutionary Trap".
To test whether this concept is cell line or drug dependent, we analyzed 21 drug-resistant tumor cell expression profiles reveal that JAG1, GPC3, and L1CAM, which are suitable targets for CAR-T treatment, are significantly upregulated in various drug-resistant tumor cells.
Our findings shed light on the feasibility of utilizing CAR-T therapy to treat drug-resistant tumors and broaden the concept of the "Evolutionary Trap".
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