Evidence map›Paper›PMID 26483965›Full record

ArticleActa naturae

Regulation of Human Adenovirus Replication by RNA Interference.

N A Nikitenko, T Speiseder, E Lam, P M Rubtsov, Kh D Tonaeva, S A Borzenok, T Dobner, V S Prassolov

Open access · hybridAbstract read
In one paragraph

Article in Acta naturae. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Stable expression of shRNA for the control of recombinant adenovirus replication.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

N A NikitenkoEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilova Str., 32, Moscow, 119991, Russia.
T SpeisederHeinrich Pette Institute - Leibniz Institute for Experimental Virology, Martinistrasse 52 D-20251, Hamburg, Germany.
E LamHeinrich Pette Institute - Leibniz Institute for Experimental Virology, Martinistrasse 52 D-20251, Hamburg, Germany.
P M RubtsovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilova Str., 32, Moscow, 119991, Russia.
Kh D TonaevaS.N. Fedorov Eye Microsurgery Complex of the Ministry of Health of the Russian Federation, Beskudnikovskiy Blvd., 59A, Moscow, 127486, Russia.
S A BorzenokS.N. Fedorov Eye Microsurgery Complex of the Ministry of Health of the Russian Federation, Beskudnikovskiy Blvd., 59A, Moscow, 127486, Russia.
T DobnerHeinrich Pette Institute - Leibniz Institute for Experimental Virology, Martinistrasse 52 D-20251, Hamburg, Germany.
V S PrassolovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilova Str., 32, Moscow, 119991, Russia.
Engelhardt Institute of Molecular Biology · RULeibniz Institute of Virology (LIV) · DEMinistry of Health of the Russian Federation · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adenoviruses cause a wide variety of human infectious diseases. Adenoviral conjunctivitis and epidemic keratoconjunctivitis are commonly associated with human species D adenoviruses. Currently, there is no sufficient or appropriate treatment to counteract these adenovirus infections. Thus, there is an urgent need for new etiology-directed therapies with selective activity against human adenoviruses. To address this problem, the adenoviral early genes E1A and E2B (viral DNA polymerase) seem to be promising targets. Here, we propose an effective approach to downregulate the replication of human species D adenoviruses by means of RNA interference. We generated E1A expressing model cell lines enabling fast evaluation of the RNA interference potential. Small interfering RNAs complementary to the E1A mRNA sequences of human species D adenoviruses mediate significant suppression of the E1A expression in model cells. Furthermore, we observed a strong downregulation of replication of human adenoviruses type D8 and D37 by small hairpin RNAs complementary to the E1A or E2B mRNA sequences in primary human limbal cells. We believe that our results will contribute to the development of efficient anti-adenoviral therapy.

Indexed as

human adenoviruseslentiviral vectorsRNA interferencesmall hairpin RNAssmall interfering RNAs

Identifiers

PMID26483965
PMCPMC4610170
OpenAlexW1787587993

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.