» Articles » PMID: 35378051

C-Met Specific CAR-T Cells As a Targeted Therapy for Non-small Cell Lung Cancer Cell A549

Overview
Journal Bioengineered
Date 2022 Apr 4
PMID 35378051
Authors
Affiliations
Soon will be listed here.
Abstract

Non-small cell lung cancer (NSCLC) is considered to be one of the most prevalent and fatal malignancies, with a poor survival rate. Chimeric antigen receptor T cell (CAR-T) cell therapy is one of the most exciting directions in the field of Cellular immunotherapy. Therefore, CAR-T cells that target c-Met have been developed for use in NSCLC therapy and might be a potential therapeutic strategy. The anti c-Met scFv structure was fused with the transmembrane and intracellular domains. Using a lentiviral vector to load the c-Met CAR gene, then transfected the c-Met CAR lentiviral into human T cells to obtain the second generation c-Met CAR-T expressing CARs stably. In vitro co-culture, experiments revealed that CAR-T cells have high proliferative activity and the potential to secrete cytokines (IL-2, TNF-α, and IFN-γ). c-Met CAR-T cells showed special cellular cytotoxicity in LDH release assay. A subcutaneous tumor model in nude mice was used to test the anticancer effectiveness of c-met CAR-T cells in vivo. For c-Met positive NSCLC tissue, according to tumor volume, weight, fluorescence intensity, and immunohistochemical detection, c-Met CAR-T cells had stronger tumor growth suppression compared to untransduced T cells. HE staining revealed that c-Met CAR-T cells did not produced side effects in nude mice. Taken together, we provided useful method to generate c-Met CAR- T cells, which exhibit enhanced cytotoxicity against NSCLC cells in vitro and in vivo. Thus, providing a new therapeutic avenue for treating NSCLC clinically. (1) c-Met CAR-T capable of stably expressing c-Met CARs were constructed.(2) c-Met CAR-T have strong anti-tumor ability and proliferation ability in vitro.(3) c-Met CAR-T can effectively inhibit the growth of A549 cells subcutaneous xenografts.

Citing Articles

MET Activation in Lung Cancer and Response to Targeted Therapies.

Okun S, Lu D, Sew K, Subramaniam A, Lockwood W Cancers (Basel). 2025; 17(2).

PMID: 39858062 PMC: 11764361. DOI: 10.3390/cancers17020281.


Addressing the unmet need in NSCLC progression with advances in second-line therapeutics.

Wang K, Leyba A, Hsu R Explor Target Antitumor Ther. 2025; 5(6):1297-1320.

PMID: 39759220 PMC: 11700623. DOI: 10.37349/etat.2024.00277.


Leveraging CAR macrophages targeting c-Met for precision immunotherapy in pancreatic cancer: insights from single-cell multi-omics.

Hu L, Wang X, Song Z, Chen F, Wu B Mol Med. 2024; 30(1):231.

PMID: 39592929 PMC: 11590533. DOI: 10.1186/s10020-024-00996-4.


[Enhanced tumoricidal activity of PD-1 antibody-secreting c-Met CAR-T cells against pancreatic cancer cells].

Min J, Peng S, Du N, An R, Zhen X, Cao J Nan Fang Yi Ke Da Xue Xue Bao. 2024; 44(10):1976-1984.

PMID: 39523098 PMC: 11526466. DOI: 10.12122/j.issn.1673-4254.2024.10.16.


Targeting the MET gene: unveiling therapeutic opportunities in immunotherapy within the tumor immune microenvironment of non-small cell lung cancer.

Ye L, Wang W, Li H, Ji Y, Le X, Xu X Ther Adv Med Oncol. 2024; 16:17588359241290733.

PMID: 39483139 PMC: 11526239. DOI: 10.1177/17588359241290733.


References
1.
Zhao Z, Xiao X, Saw P, Wu W, Huang H, Chen J . Chimeric antigen receptor T cells in solid tumors: a war against the tumor microenvironment. Sci China Life Sci. 2019; 63(2):180-205. DOI: 10.1007/s11427-019-9665-8. View

2.
Yu F, Wang X, Shi H, Jiang M, Xu J, Sun M . Development of chimeric antigen receptor-modified T cells for the treatment of esophageal cancer. Tumori. 2020; 107(4):341-352. DOI: 10.1177/0300891620960223. View

3.
Peschard P, Park M . From Tpr-Met to Met, tumorigenesis and tubes. Oncogene. 2007; 26(9):1276-85. DOI: 10.1038/sj.onc.1210201. View

4.
Miranda O, Farooqui M, Siegfried J . Status of Agents Targeting the HGF/c-Met Axis in Lung Cancer. Cancers (Basel). 2018; 10(9). PMC: 6162713. DOI: 10.3390/cancers10090280. View

5.
Liu M, Mu J, Yuan T, Cui R, Meng J, Jiang Y . [In vitro studies on the transfer of CAR into leukemia cells due to their residue in the autologous CAR-T cell preparation system for acute B-cell acute lymphoblastic leukemia]. Zhonghua Xue Ye Xue Za Zhi. 2021; 42(2):140-145. PMC: 8071665. DOI: 10.3760/cma.j.issn.0253-2727.2021.02.009. View