Evidence map›Paper›PMID 11498786›Full record

ArticleOncogene2001

Constitutive expression of ectopic c-Myc delays glucocorticoid-evoked apoptosis of human leukemic CEM-C7 cells.

R D Medh, A Wang, F Zhou, E B Thompson

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-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

17 citing papers in PubMed, 42 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

4 authors at 2 institutions in 1 country.

R D MedhDepartment of Human Biological Chemistry and Genetics, The University of Texas Medical Branch, Galveston, Texas, TX-77555-0645, USA. rmedh@utmb.edu
A Wang
F Zhou
E B Thompson
The University of Texas Medical Branch at Galveston · USLos Alamos National Laboratory · US

Funding

THE HUMAN GLUCOCORTICOID RECEPTORS, ITS GENE AND ACTIONSR01CA041407 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI THOMPSON, E B · 1986 to 2006
$1.6M
CHARACTERIZATION OF THE HUMAN C1Q RECEPTORR01CA041047 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI GHEBREHIWET, BERHANE · 1986 to 1988
–
NCI NIH HHS 2RO1 CA41047NCI NIH HHS R01 CA041407
6 · The paper itself

Abstract

Sensitivity to glucocorticoid (GC)-evoked apoptosis in lymphoid cell lines correlates closely with GC-mediated suppression of c-Myc expression. To establish a functional role for c-Myc in GC-mediated apoptosis, we have stably expressed MycER(TM), the human c-Myc protein fused to the modified ligand-binding domain of the murine estrogen receptor alpha, in GC-sensitive CEM-C7-14 cells. In CEM-C7-14 cells, MycER(TM) constitutively imparts c-Myc functions. Cells expressing MycER(TM) (C7-MycER(TM)) exhibited a marked reduction in cell death after 72 h in 100 nM dexamethasone (Dex), with 10-20-fold more viable cells when compared to the parental CEM-C7-14 clone. General GC responsiveness was not compromised, as evidenced by Dex-mediated suppression of endogenous c-Myc and cyclin D3, and induction of c-Jun and the glucocorticoid receptor. MycER(TM) also blunted Dex-mediated upregulation of p27(kipI) and suppression of the Myc target p53. In comparison to parental CEM-C7-14 cells, Dex-evoked DNA strand breaks were negligible and caspase activation was delayed, but the extent of G1 cell cycle arrest was similar in C7-MycER(TM) cells. Myc-ER(TM) did not result in permanent, complete resistance to GC however, and the GC-treated cells eventually died, indicative of redundant or interactive mechanisms in the GC-evoked lytic response of lymphoid cells. Our results emphasize the importance of c-Myc suppression in GC-evoked apoptosis of CEM-C7-14 cells.

Indexed as

ApoptosisTranscription FactorsTumor Suppressor ProteinsAntineoplastic Agents, HormonalBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBasic-Leucine Zipper Transcription FactorsBiopterinsCaspase 3CaspasesCell Cycle ProteinsClone CellsCyclin-Dependent Kinase Inhibitor p27DexamethasoneDNA-Binding ProteinsDNA DamageEstrogen Receptor alphaAntineoplastic Agents, HormonalBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBasic-Leucine Zipper Transcription FactorsBiopterinsCASP3 protein, humanCaspase 3CaspasesCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p27DexamethasoneDNA-Binding ProteinsEstrogen Receptor alphaGlucocorticoidsMAX protein, humanMyc associated factor XProto-Oncogene Proteins c-mycReceptors, EstrogenRecombinant Fusion ProteinssapropterinTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID11498786
PMCPMC2761604
OpenAlexW2021701623

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.