Evidence map›Paper›PMID 17975014›Full record

ArticleBlood2008

CREB is a critical regulator of normal hematopoiesis and leukemogenesis.

Jerry C Cheng, Kentaro Kinjo, Dejah R Judelson, Jenny Chang, Winston S Wu, Ingrid Schmid, Deepa B Shankar, Noriyuki Kasahara, Renata Stripecke, Ravi Bhatia and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

71 citing papers in PubMed, 114 citations in OpenAlex.

  1. cAMP response element-binding protein promotes gliomagenesis by modulating the expression of oncogenic microRNA-23a.Proceedings of the National Academy of Sciences of the United States of America · 2012
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  19. CaJournal of cellular immunology · 2021
    Article
  20. What turns CREB on? And off? And why does it matter?Cellular and molecular life sciences : CMLS · 2020
    Review

11 more citing papers are in PubMed but not listed here.

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

12 authors at 5 institutions in 2 countries.

Jerry C ChengDivision of Hematology/Oncology, Department of Pediatrics, Gwynne Hazen Cherry Memorial Laboratories and Mattel Children's Hospital, Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, CA 90095-1752, USA.
Kentaro Kinjo
Dejah R Judelson
Jenny Chang
Winston S Wu
Ingrid Schmid
Deepa B Shankar
Noriyuki Kasahara
Renata Stripecke
Ravi Bhatia
Elliot M Landaw
Kathleen M Sakamoto
University of California, Los Angeles · USUniversity of Colorado Denver · USUCLA Jonsson Comprehensive Cancer CenterCity of Hope · USJubilant Life Sciences (India) · IN

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CUMBERLAND, WILLIAM GLEN · 1991 to 2018
$39.9M
Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
The Role of CREB in Normal Myelopoiesis and LeukemogenesisR01HL075826 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAKAMOTO, KATHLEEN M · 2004 to 2013
$3.2M
Molecular and Cellular Characterization of Myeloproliferative DiseaseR01HL083077 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAKAMOTO, KATHLEEN M · 2005 to 2010
$1.5M
Role of CREB in Normal Hematopoiesis and AMLF32HL085013 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHENG, JERRY C · 2006 to 2006
$54k
NCI NIH HHS CA16042NCI NIH HHS P30 CA016042NHLBI NIH HHS F32 HL085013NHLBI NIH HHS HL75826NHLBI NIH HHS HL83077NHLBI NIH HHS R01 HL075826NHLBI NIH HHS R01 HL083077NIAID NIH HHS AI28697NIAID NIH HHS P30 AI028697NIDDK NIH HHS P30 DK041301
6 · The paper itself

Abstract

The cAMP-responsive element binding protein (CREB) is a 43-kDa nuclear transcription factor that regulates cell growth, memory, and glucose homeostasis. We showed previously that CREB is amplified in myeloid leukemia blasts and expressed at higher levels in leukemia stem cells from patients with myeloid leukemia. CREB transgenic mice develop myeloproliferative disease after 1 year, but not leukemia, suggesting that CREB contributes to but is not sufficient for leukemogenesis. Here, we show that CREB is most highly expressed in lineage negative hematopoietic stem cells (HSCs). To understand the role of CREB in hematopoietic progenitors and leukemia cells, we examined the effects of RNA interference (RNAi) to knock down CREB expression in vitro and in vivo. Transduction of primary HSCs or myeloid leukemia cells with lentiviral CREB shRNAs resulted in decreased proliferation of stem cells, cell- cycle abnormalities, and inhibition of CREB transcription. Mice that received transplants of bone marrow transduced with CREB shRNA had decreased committed progenitors compared with control mice. Mice injected with Ba/F3 cells expressing either Bcr-Abl wild-type or T315I mutation with CREB shRNA had delayed leukemic infiltration by bioluminescence imaging and prolonged median survival. Our results suggest that CREB is critical for normal myelopoiesis and leukemia cell proliferation.

Indexed as

HematopoiesisAnimalsCell LineCell ProliferationCyclic AMP Response Element-Binding ProteinCyclin ACyclin D1Gene Expression RegulationHumansLeukemiaMiceMice, Inbred C57BLRNA InterferenceSurvival RateCyclic AMP Response Element-Binding ProteinCyclin ACyclin D1

Identifiers

PMID17975014
PMCPMC2214769
OpenAlexW2036257162

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.