c-Met-Specific Chimeric Antigen Receptor T Cells Demonstrate Anti-Tumor Effect in c-Met Positive Gastric Cancer

被引:25
|
作者
Kang, Chung Hyo [1 ]
Kim, Yeongrin [1 ,2 ]
Lee, Da Yeon [1 ,3 ]
Choi, Sang Un [1 ]
Lee, Heung Kyoung [1 ]
Park, Chi Hoon [1 ,2 ]
机构
[1] Korea Res Inst Chem Technol, Therapeut & Biotechnol Div, Daejeon 34114, South Korea
[2] Korea Univ Sci & Technol, Med Chem & Pharmacol, Daejeon 34113, South Korea
[3] Chungnam Natl Univ, Coll Pharm, Daejeon 34134, South Korea
关键词
c-Met; gastric cancer; chimeric antigen receptor; CAR T cell; KHYG-1; GROWTH-FACTOR RECEPTOR; AMPLIFICATION; IMMUNOTHERAPY; LYMPHOMA; GENE; HGF;
D O I
10.3390/cancers13225738
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary: c-Met is known to be overexpressed in gastric cancers. Here, we developed anti-c-Met CAR T cell and measured its anti-tumor efficacy in vitro and in vivo. Our anti c-Met CAR T cells have shown selective killing of c-Met overexpressed gastric cancer cells. Based on our results, we suggest that anti-c-Met CAR T cell therapy could be effective for gastric cancer patients. Chimeric antigen receptor (CAR) technology has been highlighted in recent years as a new therapeutic approach for cancer treatment. Although the impressive efficacy of CAR-based T cell adoptive immunotherapy has been observed in hematologic cancers, limited effect has been reported on solid tumors. Approximately 20% of gastric cancer (GC) patients exhibit a high expression of c-Met. We have generated an anti c-Met CAR construct that is composed of a single-chain variable fragment (scFv) of c-Met antibody and signaling domains consisting of CD28 and CD3 zeta. To test the CAR construct, we used two cell lines: the Jurkat and KHYG-1 cell lines. These are convenient cell lines, compared to primary T cells, to culture and to test CAR constructs. We transduced CAR constructs into Jurkat cells by electroporation. c-Met CAR Jurkat cells secreted interleukin-2 (IL-2) only when incubated with c-Met positive GC cells. To confirm the lytic function of CAR, the CAR construct was transduced into KHYG-1, a NK/T cell line, using lentiviral particles. c-Met CAR KHYG-1 showed cytotoxic effect on c-Met positive GC cells, while c-Met negative GC cell lines were not eradicated by c-Met CAR KHYG-1. Based on these data, we created c-Met CAR T cells from primary T cells, which showed high IL-2 and IFN-gamma secretion when incubated with the c-Met positive cancer cell line. In an in vivo xenograft assay with NSG bearing MKN-45, a c-Met positive GC cell line, c-Met CAR T cells effectively inhibited the tumor growth of MKN-45. Our results show that the c-Met CAR T cell therapy can be effective on GC.
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页数:13
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