| Literature DB >> 17167176 |
Jan-Henrik Mikesch1, Kathrin Schier, Antje Roetger, Ronald Simon, Horst Buerger, Burkhard Brandt.
Abstract
Decay-accelerating factor (DAF, CD55) is physiologically acting as an inhibitor of the complement system, but is also broadly expressed in malignant tumours. Here DAF seems to exert different functions beyond its immunological role such as e.g. promotion of tumorigenesis, decrease of complement mediated tumor cell lysis, autocrine loops for cell rescue and evasion of apoptosis, neoangiogenesis, invasiveness, cell motility, and metastasis via oncogenic tyrosine kinase pathways and specific seven-span transmembrane receptors (CD97) binding. Therefore, DAF has already become a target for therapy. In this paper we review the role of DAF in human malignancies as described in different basic, diagnostic and experimental therapeutic studies.Entities:
Mesh:
Substances:
Year: 2006 PMID: 17167176 PMCID: PMC4618202 DOI: 10.1155/2006/814816
Source DB: PubMed Journal: Cell Oncol ISSN: 1570-5870 Impact factor: 6.730