TGF-β Superfamily Receptors—Targets for Antiangiogenic Therapy?
Author(s) -
Jasmin Otten,
Carsten Bokemeyer,
Walter Fiedler
Publication year - 2010
Publication title -
journal of oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.228
H-Index - 54
eISSN - 1687-8469
pISSN - 1687-8450
DOI - 10.1155/2010/317068
Subject(s) - tgf beta signaling pathway , medicine , receptor , cancer research , transforming growth factor beta , antibody , immunology , immune system , endoglin , transforming growth factor , microbiology and biotechnology , biology , stem cell , cd34
The TGF- β pathway controls a broad range of cellular behavior including cell proliferation, differentiation, and apoptosis of various cell types including tumor cells, endothelial cells, immune cells, and fibroblasts. Besides TGF- β 's direct effects on tumor growth and its involvement in neoangiogenesis have received recent attention. Germline mutations in TGF- β receptors or coreceptors causing Hereditary Hemorrhagic Teleangiectasia and the Loeys-Dietz syndrome underline the involvement of TGF- β in vessel formation and maturation. Several therapeutic approaches are evaluated at present targeting the TGF- β pathway including utilization of antisense oligonucleotides against TGF- β itself or antibodies or small molecule inhibitors of TGF- β receptors. Some of these therapeutic agents have already entered the clinical arena including an antibody against the endothelium specific TGF- β class I receptor ALK-1 targeting tumor vasculature. In conclusion, therapeutic manipulation of the TGF- β pathway opens great opportunities in future cancer therapy.
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