Evidence map›Paper›PMID 15565166›Full record

ArticleLeukemia2005

Induction of apoptosis by proteasome inhibitors in B-CLL cells is associated with downregulation of CD23 and inactivation of Notch2.

M Duechler, M Shehata, J D Schwarzmeier, A Hoelbl, M Hilgarth, R Hubmann

Abstract read
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In one paragraph

Article in Leukemia, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

33 citing papers in PubMed, 75 citations in OpenAlex.

  1. Phase II study of dasatinib in relapsed or refractory chronic lymphocytic leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Trial
  2. Trial
  3. Bortezomib-mediated inhibition of steroid receptor coactivator-3 degradation leads to activated Akt.Clinical cancer research : an official journal of the American Association for Cancer Research · 2008
    Trial
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. High-Risk Mantle Cell Lymphoma in the Era of Novel Agents.Current hematologic malignancy reports · 2021
    Review
  11. Article
  12. Review
  13. Cancer Stem Cells,Cells · 2020
    Review
  14. Therapeutic Targeting of Notch Signaling Pathway in Hematological Malignancies.Mediterranean journal of hematology and infectious diseases · 2019
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
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 1 country.

M DuechlerLudwig Boltzmann Institute for Cytokine Research, Medical University Vienna, Vienna, Austria.
M Shehata
J D Schwarzmeier
A Hoelbl
M Hilgarth
R Hubmann
Ludwig Boltzmann Institute for Cancer Research · ATMedical University of Vienna · ATLudwig Boltzmann Institute for Digital Health and Prevention

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, proteasome inhibitors (PI) have attracted interest as novel anticancer agents in B-cell chronic lymphocytic leukemia (B-CLL). A prominent feature of B-CLL cells is the high expression of CD23, which is closely related to cell survival and is regulated by Notch2. Since several components of the Notch signaling cascade are tightly regulated by proteasomal degradation, we studied the effect of PI on Notch2 activity and CD23 expression. Exposure of B-CLL cells to PI led to induction of apoptosis, a time- and dose-dependent downregulation of CD23 expression and a decline in DNA binding of transcriptionally active Notch2. In contrast, the transcription factor NF-AT and its putative target gene CD5, which is highly expressed in B-CLL cells, were unaffected. When the late phase of PI-induced apoptosis was arrested by inhibition of caspase 3, the reduction of Notch2 activity was still observed, indicating that reduction of active Notch2 took place already during an earlier phase of apoptosis. Enforced expression of constitutively active Notch2 decreased PI-mediated apoptosis in a human B-cell line. These data indicate that downregulation of CD23 and loss of Notch2 activity are early steps in PI-induced apoptosis of B-CLL lymphocytes and may be part of the full apoptotic response.

Indexed as

Proteasome InhibitorsAntigens, CDAntineoplastic AgentsApoptosisBase SequenceBoronic AcidsBortezomibCell Line, TumorDNA PrimersGene Expression Regulation, NeoplasticHumansLeukemia, Lymphocytic, Chronic, B-CellProtease InhibitorsPyrazinesReceptor, Notch2Receptors, Cell SurfaceAntigens, CDAntineoplastic AgentsBoronic AcidsBortezomibDNA PrimersNOTCH2 protein, humanProtease InhibitorsProteasome InhibitorsPyrazinesReceptor, Notch2Receptors, Cell SurfaceReceptors, IgERNA, Messenger

Identifiers

PMID15565166
OpenAlexW2064172582

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.