Unknown

Dataset Information

0

Targeting CD24 in Cancer Immunotherapy.


ABSTRACT: Immunotherapy is a hot area in cancer treatment, and one of the keys to this therapy is the identification of the right tumour-associated or tumour-specific antigen. Cluster of differentiation 24 (CD24) is an emerging tumour-associated antigen that is commonly and highly expressed in various tumours. In addition, CD24 is associated with several cancer-related signalling pathways and closely interacts with other molecules and immune cells to influence tumour progression. Monoclonal antibodies, antibody-drug conjugates (ADCs), chimeric antigen receptor (CAR) T-cell therapy, and CAR-NK cell therapy are currently available for the treatment of CD24. In this review, we summarise the existing therapeutic approaches and possible future directions targeting CD24.

SUBMITTER: Chen W 

PROVIDER: S-EPMC10740697 | biostudies-literature | 2023 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Targeting CD24 in Cancer Immunotherapy.

Chen Wenwen W   Hu Zhigang Z   Guo Zhigang Z  

Biomedicines 20231127 12


Immunotherapy is a hot area in cancer treatment, and one of the keys to this therapy is the identification of the right tumour-associated or tumour-specific antigen. Cluster of differentiation 24 (CD24) is an emerging tumour-associated antigen that is commonly and highly expressed in various tumours. In addition, CD24 is associated with several cancer-related signalling pathways and closely interacts with other molecules and immune cells to influence tumour progression. Monoclonal antibodies, an  ...[more]

Similar Datasets

| S-EPMC10623753 | biostudies-literature
| S-EPMC10821995 | biostudies-literature
| S-EPMC9409925 | biostudies-literature
| S-EPMC11129509 | biostudies-literature
| S-EPMC6697206 | biostudies-literature
| S-EPMC6006764 | biostudies-literature
| S-EPMC8317330 | biostudies-literature
| S-EPMC7513516 | biostudies-literature
| S-EPMC7994399 | biostudies-literature
| S-EPMC8557524 | biostudies-literature