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Improved replication efficiency of echovirus 5 after transfection of colon cancer cells using an authentic 5' RNA genome end methodology

Israelsson, Stina (author)
Linnéuniversitetet,Institutionen för biologi och miljö (BOM)
Sävneby, Anna, 1985- (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Picorna
Ekström, Jens-Ola (author)
Linnéuniversitetet,Institutionen för biologi och miljö (BOM),Umeå universitet
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Jonsson, Nina (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB)
Edman, Kjell (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB)
Lindberg, A. Michael (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB)
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 (creator_code:org_t)
2014-07-23
2014
English.
In: Investigational new drugs. - : Springer Science and Business Media LLC. - 0167-6997 .- 1573-0646. ; 32:6, s. 1063-1070
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Oncolytic virotherapy is a promising novel form of cancer treatment, but the therapeutic efficiency needs improvement. A potential strategy to enhance the therapeutic effect of oncolytic viruses is to use infectious nucleic acid as therapeutic agent to initiate an oncolytic infection, without administrating infectious viral particles. Here we demonstrate improved viral replication activation efficiency when transfecting cells with 5’ end authentic in vitro transcribed enterovirus RNA as compared to genomic RNA with additional non-genomic 5’ nucleotides generated by conventional cloning methods. We used echovirus 5 (E5) as an oncolytoc model virus due to its ability to replicate in and completely destroy five out of six colon cancer cell lines and kill artificial colon cancer tumors (HT29 spheroids), as shown here. An E5 infectious cDNA clone including a hammerhead ribozyme sequence was used to generate in vitro transcripts with native 5’ genome ends. In HT29 cells, activation of virus replication is approximately 20-fold more efficient for virus genome transcripts with native 5’ genome ends compared to E5 transcripts generated from a standard cDNA clone. This replication advantage remains when viral progeny release starts by cellular lysis 22 h post transfection. Hence, a native 5’ genomic end improves infection activation efficacy of infectious nucleic acid, potentially enhancing its therapeutic effect when used for cancer treatment. The clone design with a hammerhead ribozyme is likely to be applicable to a variety of oncolytic positive sense RNA viruses for the purpose of improving the efficacy of oncolytic virotherapy.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Picornavirus
RNA virus
Enterovirus
Oncolytic virotherapy
Hammerhead ribozyme
Infectious nucleic acid
Virologi
Virology

Publication and Content Type

ref (subject category)
art (subject category)

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