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Expand available targets for CAR-T therapy to overcome tumor drug resistance based on the "Evolutionary Traps".
- Source :
-
Pharmacological research [Pharmacol Res] 2024 Jun; Vol. 204, pp. 107221. Date of Electronic Publication: 2024 May 18. - Publication Year :
- 2024
-
Abstract
- 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".<br />Competing Interests: Declaration of Competing Interest The authors declare no conflict interests.<br /> (Copyright © 2024. Published by Elsevier Ltd.)
- Subjects :
- Humans
Animals
Cell Line, Tumor
Lapatinib pharmacology
Lapatinib therapeutic use
Neoplasms drug therapy
Neoplasms genetics
Neoplasms therapy
Receptors, Chimeric Antigen genetics
Receptors, Chimeric Antigen immunology
Mice, Nude
Mice, Inbred BALB C
Mice
Female
Drug Resistance, Neoplasm
Antineoplastic Agents pharmacology
Antineoplastic Agents therapeutic use
Immunotherapy, Adoptive methods
Subjects
Details
- Language :
- English
- ISSN :
- 1096-1186
- Volume :
- 204
- Database :
- MEDLINE
- Journal :
- Pharmacological research
- Publication Type :
- Academic Journal
- Accession number :
- 38768669
- Full Text :
- https://doi.org/10.1016/j.phrs.2024.107221