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Targeting HER3 using mono- and bispecific antibodies or alternative scaffolds
KTH, School of Biotechnology (BIO), Protein Technology.ORCID iD: 0000-0003-1763-9073
KTH, School of Biotechnology (BIO), Protein Technology.ORCID iD: 0000-0002-9282-0174
KTH, School of Biotechnology (BIO), Protein Technology.ORCID iD: 0000-0001-9423-0541
2016 (English)In: mAbs, ISSN 1942-0862, E-ISSN 1942-0870, Vol. 8, no 7, 1195-1209 p.Article in journal (Refereed) Published
Abstract [en]

The human epidermal growth factor receptor 3 (HER3) has in recent years been recognized as a key node in the complex signaling network of many different cancers. It is implicated in de novo and acquired resistance against therapies targeting other growth factor receptors, e.g., EGFR, HER2, and it is a major activator of the PI3K/Akt signaling pathway. Consequently, HER3 has attracted substantial attention, and is today a key target for drugs in clinical development. Sophisticated protein engineering approaches have enabled the generation of a range of different affinity proteins targeting this receptor, including antibodies and alternative scaffolds that are either mono- or bispecific. Here, we describe HER3 and its role as a key tumor target, and give a comprehensive review of HER3-targeted proteins currently in development, including discussions on the opportunities and challenges of targeting this receptor.

Place, publisher, year, edition, pages
Taylor & Francis, 2016. Vol. 8, no 7, 1195-1209 p.
Keyword [en]
Affibody molecules, alternative scaffolds, bispecific antibodies, ErbB3, HER3, monoclonal antibodies, protein therapeutics, tumor targeting
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:kth:diva-195263DOI: 10.1080/19420862.2016.1212147ISI: 000385569400002ScopusID: 2-s2.0-84989339198OAI: oai:DiVA.org:kth-195263DiVA: diva2:1046866
Note

QC 20161115

Available from: 2016-11-15 Created: 2016-11-02 Last updated: 2016-11-15Bibliographically approved

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Malm, MagdalenaStåhl, StefanLöfblom, John
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CiteExportLink to record
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Citation style
  • apa
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