Evidence map›Paper›PMID 28928217›Full record

ArticleThe Journal of biological chemistry2017

Peptides derived from evolutionarily conserved domains in Beclin-1 and Beclin-2 enhance the entry of lentiviral vectors into human cells.

Saliha Majdoul, Jeremie Cosette, Ababacar K Seye, Eric Bernard, Sophie Frin, Nathalie Holic, Nathalie Chazal, Laurence Briant, Lucile Espert, Anne Galy and 1 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Saliha MajdoulFrom Integrare Research Unit, UMR_S951, Généthon, INSERM, University of Evry, EPHE, Evry F 91000, France.
Jeremie CosetteGénéthon, 91000 Evry, France, and.
Ababacar K SeyeFrom Integrare Research Unit, UMR_S951, Généthon, INSERM, University of Evry, EPHE, Evry F 91000, France.
Eric BernardIRIM (ex-CPBS) UMR 9004, Infectious Disease Research Institute of Montpellier, University of Montpellier, CNRS, Montpellier F34293, France.
Sophie FrinFrom Integrare Research Unit, UMR_S951, Généthon, INSERM, University of Evry, EPHE, Evry F 91000, France.
Nathalie HolicFrom Integrare Research Unit, UMR_S951, Généthon, INSERM, University of Evry, EPHE, Evry F 91000, France.
Nathalie ChazalIRIM (ex-CPBS) UMR 9004, Infectious Disease Research Institute of Montpellier, University of Montpellier, CNRS, Montpellier F34293, France.
Laurence BriantIRIM (ex-CPBS) UMR 9004, Infectious Disease Research Institute of Montpellier, University of Montpellier, CNRS, Montpellier F34293, France.
Lucile EspertIRIM (ex-CPBS) UMR 9004, Infectious Disease Research Institute of Montpellier, University of Montpellier, CNRS, Montpellier F34293, France.
Anne GalyFrom Integrare Research Unit, UMR_S951, Généthon, INSERM, University of Evry, EPHE, Evry F 91000, France, galy@genethon.fr.ORCID 0000-0002-0153-4392
David FenardFrom Integrare Research Unit, UMR_S951, Généthon, INSERM, University of Evry, EPHE, Evry F 91000, France, david.fenard@txcell.com.ORCID 0000-0003-0242-386X
Inserm · FRCentre National de la Recherche Scientifique · FRGenethon (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy-related proteins such as Beclin-1 are involved in an array of complex processes, including antiviral responses, and may also modulate the efficiency of gene therapy viral vectors. The Tat-Beclin-1 (TB1) peptide has been reported as an autophagy-inducing factor inhibiting the replication of pathogens such as HIV, type 1 (HIV-1). However, autophagy-related proteins are also essential for the early steps of HIV-1 infection. Therefore, we examined the effects of the Beclin-1 evolutionarily conserved domain in TB1 on viral transduction and autophagy in single-round HIV infection or with nonreplicative HIV-1-derived lentiviral vectors. TB1 enhanced transduction with various pseudotypes but without inducing the autophagy process. TB1 augmented the transduction of human CD34+ hematopoietic stem/progenitor cells while maintaining their capacity to engraft

Indexed as

AutophagyVirus InternalizationAmino Acid SequenceAnimalsBeclin-1Cell Line, TransformedCell Line, TumorCells, CulturedConserved SequenceGenetic TherapyHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHIV-1HumansIntracellular Signaling Peptides and ProteinsLentivirusBeclin-1BECN1 protein, humanBECN2 protein, humanIntracellular Signaling Peptides and ProteinsPeptide FragmentsRecombinant Fusion Proteinstat Gene Products, Human Immunodeficiency VirusautophagyBeclin1 (BECN1)gene therapyhematopoietic stem cellslentivirusvirus entry

Identifiers

PMID28928217
PMCPMC5682973
OpenAlexW2755074867

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.