Evidence map›Paper›PMID 10888626›Full record

ArticleJournal of virology2000

Differences in the ability of human T-cell lymphotropic virus type 1 (HTLV-1) and HTLV-2 tax to inhibit p53 function.

R Mahieux, C A Pise-Masison, P F Lambert, C Nicot, L De Marchis, A Gessain, P Green, W Hall, J N Brady

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

31 citing papers in PubMed, 51 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

9 authors at 5 institutions in 3 countries.

R MahieuxLaboratory of Receptor Biology and Gene Expression,National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
C A Pise-Masison
P F Lambert
C Nicot
L De Marchis
A Gessain
P Green
W Hall
J N Brady
Gene Therapy Laboratory · FRInstitut Pasteur · FRNational Cancer Institute · USThe Ohio State University · USUniversity College Dublin · IE

Funding

INTERACTION OF HTLV-I TAX WITH CELLULAR REGULATORY PROTEINSZ01BC005691 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BRADY, JOHN N. · 1996 to 2008
$2.3M
REGULATION OF VIRAL AND CELLULAR GENE EXPRESSONZ01BC005254 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BRADY, JOHN N. · 1996 to 2008
$1.1M
Inhibition of p53 Tumor Suppressor Function by HTLV-IZIABC005691 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BRADY, JOHN N. · 2009 to 2009
$709k
Regulation of HTLV-I TranscriptionZIABC005254 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BRADY, JOHN N. · 2009 to 2009
$532k
6 · The paper itself

Abstract

We have analyzed the functional activity of the p53 tumor suppressor in human T-cell lymphotropic virus type 2 (HTLV-2)-transformed cells. Abundant levels of the p53 protein were detected in both HTLV-2A and -2B virus-infected cell lines. The p53 was functionally inactive, however, both in transient-transfection assays using a p53 reporter plasmid and in induction of p53-responsive genes in response to gamma irradiation. We further investigated HTLV-2A Tax and HTLV-2B Tax effects on p53 activity. Interestingly, although Tax-2A and -2B inactivate p53, the Tax-2A protein appears to inhibit p53 function less efficiently than either Tax-1 or Tax-2B. In transient-cotransfection assays, Tax-1 and Tax-2B inactivated p53 by 80%, while Tax2A reduced p53 activity by 20%. In addition, Tax-2A does not increase the steady-state level of cellular p53 as well as Tax-1 or -2B does in the same assays. Cotransfection assays demonstrated that Tax-2A could efficiently transactivate CREB-responsive promoters to the same level as Tax-1 and Tax-2B, indicating that the protein was functional. This report provides evidence of the first functional difference between the HTLV-2A and -2B subtypes. This comparison of the action of HTLV-1 and HTLV-2 Tax proteins on p53 function will provide important insights into the mechanism of HTLV transformation.

Indexed as

Cell Transformation, ViralCell Line, TransformedGamma RaysGene Expression RegulationGene Products, taxHTLV-II InfectionsHumansHuman T-lymphotropic virus 1Human T-lymphotropic virus 2Jurkat CellsPhosphorylationT-LymphocytesTranscription, GeneticTumor Suppressor Protein p53Gene Products, taxTumor Suppressor Protein p53

Identifiers

PMID10888626
PMCPMC112204
OpenAlexW2112255391

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.