2022
DOI: 10.3389/fimmu.2022.904137
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Recent advances in CAR-T cells therapy for colorectal cancer

Abstract: Colorectal cancer (CRC) is the third most common cancer, with a high mortality rate and a serious impact on people’s life and health. In recent years, adoptive chimeric antigen receptor T (CAR-T) cells therapy has shown well efficacy in the treatment of hematological malignancies, but there are still many problems and challenges in solid tumors such as CRC. For example, the tumor immunosuppressive microenvironment, the low targeting of CAR-T cells, the short time of CAR-T cells in vivo, and the limited prolife… Show more

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Cited by 16 publications
(6 citation statements)
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“…Since the rapid development of CRISPR-Cas9 technology, the use of chimeric antigen receptor-T (CAR-T) cells is the other strategy to target specific tumor-associated antigens[ 20 ]. Although a total of 25 CAR-T cell clinical trials for CRC are ongoing as of 2022[ 21 ], the application of CAR-T cell therapy to CRC faces a challenge because of the limited infiltration of CAR-T cells to the local tumor tissues, as discussed in detail[ 20 ]. This lack of infiltration is a major challenge in the application of CAR-T therapy to solid tumors in general.…”
Section: Long Way To Developing Effective Immunotherapy For Crcmentioning
confidence: 99%
“…Since the rapid development of CRISPR-Cas9 technology, the use of chimeric antigen receptor-T (CAR-T) cells is the other strategy to target specific tumor-associated antigens[ 20 ]. Although a total of 25 CAR-T cell clinical trials for CRC are ongoing as of 2022[ 21 ], the application of CAR-T cell therapy to CRC faces a challenge because of the limited infiltration of CAR-T cells to the local tumor tissues, as discussed in detail[ 20 ]. This lack of infiltration is a major challenge in the application of CAR-T therapy to solid tumors in general.…”
Section: Long Way To Developing Effective Immunotherapy For Crcmentioning
confidence: 99%
“…Notably, all data regarding clinical trials of CAR-T therapy for CRC were collected from ClinicalTrials.gov; thus, only ClinicalTrials.gov-registered trials were included. Human epidermal growth factor receptor 2 (HER2), epithelial cell adhesion molecule (EpCAM), and mesothelin (MSLN) antigens along with NK group 2 member D ligand (NKG2DL), MUC-1, and CD133 have been licensed for use in clinical trials ( Table 2 ) because they are among the most overexpressed antigens in patients with CRC ( 107 ). Figure 2B provides a concise depiction of the T cell engineering process, illustrating the formation of CAR and TCR-T cells.…”
Section: Gene-modified T Cell Therapymentioning
confidence: 99%
“…Tai pasiekiama į T limfocitus įterpiant specialius receptorius (CAR -chimerozinis antigenų receptorius), kurie leidžia labiau orientuotis į vėžines ląsteles ir jas atakuoti. Minėtas metodas plačiai tiriamas įvairiems vėžio tipams gydyti, įskaitant kolorektalinį vėžį [46][47][48].…”
Section: Storosios žArnos Vėžio Gydymasunclassified