Abstract
CD24 was first described in the early 1980s and only attributed to scattered publications, referred to as a cell surface molecule in hematopoiesis. Recently, studies are accumulating to show that CD24 conveys a function in cell-to-cell interaction and regulation of proliferation and adhesion. CD24 appears to be highly expressed in a large variety of human cancers and to contribute to the acceleration of tumor growth and metastases shedding by binding to platelet (P)-selectin, L1 and by evoking - to date unknown - intracellular signal pathways. Anti-CD24 monoclonal antibodies thus act as a promising cancer treatment as was shown in the setting of gastrointestinal cancers. Recent articles also correlate CD24 expression with the identification of 'tumor stem cells'.
Original language | English |
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Pages (from-to) | 125-133 |
Number of pages | 9 |
Journal | Expert Review of Gastroenterology and Hepatology |
Volume | 2 |
Issue number | 1 |
DOIs | |
State | Published - Feb 2008 |
Keywords
- Cancer treatment
- CD24
- GI cancer
- Monoclonal antibody
- Oncogene
- P-selectin
- Signal transduction
- Tumor stem cell