Evidence map›Paper›PMID 10567231›Full record

ArticleThe Biochemical journal1999

Heat-shock protein 70 antisense oligomers enhance proteasome inhibitor-induced apoptosis.

J D Robertson, K Datta, S S Biswal, J P Kehrer

Open access · greenAbstract read
In one paragraph

Article in The Biochemical journal, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 64 citations in OpenAlex.

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  10. Are heat shock proteins therapeutic target for Parkinson's disease?International journal of biological sciences · 2006
    Review
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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

4 authors at 1 institution in 1 country.

J D RobertsonDivision of Pharmacology, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712-1074, USA.
K Datta
S S Biswal
J P Kehrer
Austin College · US

Funding

Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI STROM, SARA S. · 1996 to 2011
$16.4M
CELLULAR REDUCING EQUIVALENTS AND OXIDATIVE STRESSR01HL051005 · NHLBI · UNIVERSITY OF TEXAS AUSTIN · PI KEHRER, JAMES P · 1994 to 1998
–
NHLBI NIH HHS HL51005NIEHS NIH HHS ES07784
6 · The paper itself

Abstract

Recent evidence supports a role for heat-shock protein 70 (hsp70) and the 26 S proteasome in regulating apoptosis, although the precise nature of their involvement is not known. In the present study, control and Bcl-x(L)-overexpressing, interleukin-3-dependent FL5.12 cell lines were treated with the proteasome inhibitor N-benzoyloxycarbonyl (Z)-Leu-Leu-leucinal (MG132). Basal proteasome activity appeared to be approximately 30% lower in bcl-x(L) cells compared with control cells using a substrate for the chymotrypsin-like activity. However, no difference in proteasome activity was detected using substrates for the trypsin-like or peptidylglutamyl peptide-hydrolysing activities. In addition, protein levels of the 20 S proteasome beta-subunit, as determined by Western blot analyses, were similar in control and bcl-x(L) cells, leading to the conclusion that proteasome activities were the same in these two cell lines. At 24 h after treatment with 500 nM MG132, apoptosis in bcl-x(L) cells (22%) was less than that observed in control cells (34%). Concomitantly, caspase activity in control cells, as assessed by N-acetyl-l-aspartyl-l-glutamyl-l-valyl-l-aspartyl-7-amino-4-methylcou marin (Ac-DEVD-AMC), was twice that observed in bcl-x(L) cells. By 48 h after MG132 treatment, apoptosis and caspase activity in bcl-x(L) cells were similar to those observed in control cells at 24 h. Proteasome inhibition stimulated increases in hsp70 protein levels in control and bcl-x(L) cells by 12 h, although the maximal increases found in bcl-x(L) cells were less. Blocking this induction with hsp70 antisense oligonucleotides potentiated apoptosis after treatment with MG132. Inhibiting caspase activity with a broad-spectrum caspase inhibitor, t-butoxycarbonyl-Asp(OMe)-fluoromethyl ketone, prevented MG132-induced apoptosis. The more specific caspase-3 inhibitor, Ac-DEVD-aldehyde, afforded less protection, although both inhibitors completely inhibited Ac-DEVD-AMC cleavage. These data indicate that both hsp70 and Bcl-x(L) provide some protection against proteasome inhibitor-induced apoptosis.

Indexed as

ApoptosisAcetylcysteineAnimalsbcl-X ProteinB-LymphocytesCanavanineCaspase InhibitorsCaspasesCysteine EndopeptidasesCysteine Proteinase InhibitorsDrug SynergismEnzyme ActivationHematopoietic Stem CellsHSP70 Heat-Shock ProteinsInterleukin-3LeupeptinsAcetylcysteineBcl2l1 protein, mousebcl-X Proteinbenzyloxycarbonylleucyl-leucyl-leucine aldehydeCanavanineCaspase InhibitorsCaspasesCysteine EndopeptidasesCysteine Proteinase InhibitorsHSP70 Heat-Shock ProteinsInterleukin-3lactacystinLeupeptinsMultienzyme ComplexesOligonucleotides, AntisenseProteasome Endopeptidase ComplexProto-Oncogene Proteins c-bcl-2

Identifiers

PMID10567231
PMCPMC1220666
OpenAlexW2072354162

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.