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基于「进化陷阱」拓展 CAR-T 疗法可用靶点以克服肿瘤耐药

英文原题:Expand available targets for CAR-T therapy to overcome tumor drug resistance based on the "Evolutionary Traps".

查看英文原题

Expand available targets for CAR-T therapy to overcome tumor drug resistance based on the "Evolutionary Traps".

PubMed 2024/05/18(内容时间) Pharmacol Res Q1 · IF 12.2(JCR 2025)

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中文摘要

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。

展开英文摘要原文

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".

论文信息

作者
Wang X、Wang P、Liao Y、Zhao X、Hou R、Li S、Guan Z、Jin Y
第一作者单位
Cancer Institute, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, Jiangsu 221004, China; Center of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, 99 Huaihai Road, Xuzhou, Jiangsu 221002, China; Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, Jiangsu 221004, China.China
通讯作者单位
Cancer Institute, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, Jiangsu 221004, China; Center of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, 99 Huaihai Road, Xuzhou, Jiangsu 221002, China; Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, Jiangsu 221004, China. Electronic address: mingshi@xzhmu.edu.cn.China
期刊
Pharmacological research2024 Jun
原文标识
PubMed 38768669 · DOI 10.1016/j.phrs.2024.107221