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Oncolytic adenoviru...
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Leja, JustynaUppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
(author)
Oncolytic adenovirus modified with somatostatin motifs for selective infection of neuroendocrine tumor cells
- Article/chapterEnglish2011
Publisher, publication year, extent ...
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2011-04-14
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Springer Science and Business Media LLC,2011
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:uu-146964
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-146964URI
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https://doi.org/10.1038/gt.2011.54DOI
Supplementary language notes
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Language:English
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Summary in:English
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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We have previously described the oncolytic adenovirus, Ad(CgA-E1A-miR122), herein denoted Ad5(CgA-E1A-miR122) that selectively replicates in and kills neuroendocrine cells, including freshly isolated midgut carcinoid cells from liver metastases. Ad5(CgA-E1A-miR122) is based on human adenovirus serotype 5 (Ad5) and infects target cells by binding to the coxsackie-adenovirus receptor (CAR) and integrins on the cell surface. Some neuroendocrine tumor (NET) and neuroblastoma cells express low levels of CAR and are therefore poorly transduced by Ad5. However, they often express high levels of somatostatin receptors (SSTRs). Therefore, we introduced cyclic peptides, which contain four amino acids (FWKT) and mimic the binding site for SSTRs in the virus fiber knob. We show that FWKT-modified Ad5 binds to SSTR2 on NET cells and transduces midgut carcinoid cells from liver metastases about 3-4 times better than non-modified Ad5 while it transduces normal hepatocytes at about 50% of Ad5. Moreover, FWKT-modified Ad5 overcomes neutralization in an ex vivo human blood loop model to greater extent than Ad5, indicating that fiber knob modification may prolong the systematic circulation time. We conclude that modification of adenovirus with the FWKT motif may be beneficial for NET therapy.
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Added entries (persons, corporate bodies, meetings, titles ...)
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Yu, DiUppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)diayu422
(author)
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Nilsson, BerithUppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)benil498
(author)
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Gedda, LarsUppsala universitet,Enheten för biomedicinsk strålningsvetenskap(Swepub:uu)larsgedd
(author)
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Zieba, AgataUppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)agazi628
(author)
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Hakkarainen, TanjaUniversity of Helsinki, Finnish Institute for Molecular Medicine
(author)
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Åkerström, GöranUppsala universitet,Endokrinkirurgi(Swepub:uu)goranas
(author)
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Öberg, KjellUppsala universitet,Institutionen för medicinska vetenskaper(Swepub:uu)kjellob
(author)
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Giandomenico, ValeriaUppsala universitet,Institutionen för medicinska vetenskaper(Swepub:uu)valegian
(author)
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Essand, MagnusUppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)magnessa
(author)
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Uppsala universitetKlinisk immunologi
(creator_code:org_t)
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In:Gene Therapy: Springer Science and Business Media LLC18:11, s. 1052-10620969-71281476-5462
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Leja, Justyna
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Yu, Di
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Nilsson, Berith
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Gedda, Lars
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Zieba, Agata
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Hakkarainen, Tan ...
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Åkerström, Göran
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Öberg, Kjell
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Giandomenico, Va ...
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Essand, Magnus
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Gene Therapy
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