Evidence map›Paper›PMID 20152808›Full record

ArticleBiochemical and biophysical research communications2010

An antiviral disulfide compound blocks interaction between arenavirus Z protein and cellular promyelocytic leukemia protein.

C C García, I Topisirovic, M Djavani, K L B Borden, E B Damonte, M S Salvato

Open access · bronzeAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 25 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

6 authors at 3 institutions in 3 countries.

C C GarcíaLaboratory of Virology, Department of Biological Chemistry, School of Sciences, University of Buenos Aires, 1428 Buenos Aires, Argentina.
I Topisirovic
M Djavani
K L B Borden
E B Damonte
M S Salvato
Université de Montréal · CAUniversity of Buenos Aires · ARUniversity of Maryland, Baltimore · US

Funding

Protection of vaccine immunity by inhibiting Fas/FasL signalingRC2CA149001 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI SALVATO, MARIA S. · 2009 to 2010
$985k
Early Response to Hemorrhagic Fever-Causing ArenavirusesR21AI053619 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI SALVATO, MARIA S. · 2002 to 2003
$409k
Early Response to Agents Causing Flu Like SymptomsR21AI053620 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI SALVATO, MARIA S. · 2002 to 2003
$409k
ANTI-IDIOTYPE MODULATION OF HTLV-III INFECTIONU01AI023619 · NIAID · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI KENNEDY, RONALD C. · 1986 to 1988
–
NCI NIH HHS RC2 CA149001NIAID NIH HHS AI23619NIAID NIH HHS AI53620NIAID NIH HHS R21 AI053619NIAID NIH HHS R21 AI053620PHS HHS 80728
6 · The paper itself

Abstract

The promyelocytic leukemia protein (PML) forms nuclear bodies (NB) that can be redistributed by virus infection. In particular, lymphocytic choriomeningitis virus (LCMV) influences disruption of PML NB through the interaction of PML with the arenaviral Z protein. In a previous report, we have shown that the disulfide compound NSC20625 has antiviral and virucidal properties against arenaviruses, inducing unfolding and oligomerization of Z without affecting cellular RING-containing proteins such as the PML. Here, we further studied the effect of the zinc-finger-reactive disulfide NSC20625 on PML-Z interaction. In HepG2 cells infected with LCMV or transiently transfected with Z protein constructs, treatment with NSC20625 restored PML distribution from a diffuse-cytoplasmic pattern to punctate, discrete NB which appeared identical to NB found in control, uninfected cells. Similar results were obtained in cells transfected with a construct expressing a Z mutant in zinc-binding site 2 of the RING domain, confirming that this Z-PML interaction requires the integrity of only one zinc-binding site. Altogether, these results show that the compound NSC20625 suppressed Z-mediated PML NB disruption and may be used as a tool for designing novel antiviral strategies against arenavirus infection.

Indexed as

Antiviral AgentsArenaviridae InfectionsCarrier ProteinsCell LineDisulfidesGuanidinesHumansIntracellular Signaling Peptides and ProteinsLymphocytic choriomeningitis virusNuclear ProteinsPromyelocytic Leukemia ProteinTranscription FactorsTumor Suppressor ProteinsAntiviral AgentsCarrier ProteinsDisulfidesGuanidinesIntracellular Signaling Peptides and ProteinsNSC 20625Nuclear Proteinsp11 Z protein, Lymphocytic choriomeningitis virusPML protein, humanPromyelocytic Leukemia ProteinTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID20152808
PMCPMC2852548
OpenAlexW1991906262

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.