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Engineered affinity proteins for tumour-targeting applications

Friedman, Mikaela (författare)
KTH,Molekylär Bioteknologi
Ståhl, Stefan (författare)
KTH,Molekylär Bioteknologi
 (creator_code:org_t)
Wiley, 2009
2009
Engelska.
Ingår i: Biotechnology and applied biochemistry. - : Wiley. - 0885-4513 .- 1470-8744. ; 53, s. 1-29
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
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  • Targeting of tumour-associated antigens is an expanding treatment modality in clinical oncology as an alternative to, or in combination with, conventional treatments, such as chemotherapy, external-radiation therapy and surgery. Targeting of antigens that are unique or more highly expressed in tumours than in normal tissues can be used to increase the specificity and reduce the cytotoxic effect on normal tissues. Several targeting agents have been studied for clinical use, where monoclonal antibodies have been the ones most widely used. More than 20 monoclonal antibodies are approved for therapy today and the largest field is oncology. Advances in genetic engineering and in vitro selection technology has enabled the feasible high-throughput generation of monoclonal antibodies, antibody derivatives [e.g. scFvs, Fab molecules, dAbs (single-domain antibodies), diabodies and minibodies] and more recently also non-immunoglobulin scaffold proteins. Several of these affinity proteins have been investigated for both in vivo diagnostics and therapy. Affinity proteins in tumour-targeted therapy can affect tumour progression by altering signal transduction or by delivering a payload of toxin, drug or radionuclide. The ErbB receptor family has been extensively studied as biomarkers in tumour targeting, primarily for therapy using monoclonal antibodies. Two receptors in the ErbB family, EGFR (epidermal growth factor receptor) and HER2 (epidermal growth factor receptor 2), are over-expressed in various malignancies and associated with poor patient prognosis and are therefore interesting targets for solid turnours. In the present review, strategies are described for tumour targeting of solid turnours using affinity proteins to deliver radionuclides, either for molecular imaging or radiotherapy. Antibodies, antibody derivatives and non-immunoglobulin scaffold proteins are discussed with a certain focus on the affibody (Affibody (R)) molecule.

Nyckelord

affibody molecule (Affibody (R) molecule)
affinity proteins
epidermal-growth-factor-receptor family (ErbB family)
molecular
imaging
radiotherapy
tumour targeting
growth-factor-receptor
single-chain fv
ankyrin repeat protein
dependent cellular cytotoxicity
positron-emission-tomography
binding
affibody molecule
yeast surface display
human breast-cancer
complementarity-determining regions
anchored periplasmic expression

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