Evidence map›Paper›PMID 18574026›Full record

ArticleBlood2008

TAT-mediated intracellular delivery of NPM-derived peptide induces apoptosis in leukemic cells and suppresses leukemogenesis in mice.

Yun Zhou, Wei Du, Tara Koretsky, Grover C Bagby, Qishen Pang

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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. The one thousand and one chaperones of the NF-κB pathway.Cellular and molecular life sciences : CMLS · 2020
    Review
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  19. Dysregulation of the C/EBPalpha differentiation pathway in human cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2009
    Review
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

5 authors at 2 institutions in 1 country.

Yun ZhouDivision of Experimental Hematology, Cincinnati Children's Hospital Medical Center, OH 45229, USA.
Wei Du
Tara Koretsky
Grover C Bagby
Qishen Pang
Cincinnati Children's Hospital Medical Center · USOregon Health & Science University · US

Funding

Xenograft CoreP01HL048546 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI FLEMING, WILLIAM H · 1994 to 2020
$36.4M
Role of FA Proteins in HematopoiesisR01HL076712 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI PANG, QISHEN · 2005 to 2020
$5.0M
Microarray Program for NHLBI InvestigatorsR01HL072321 · NHLBI · OREGON HEALTH AND SCIENCE UNIVERSITY · PI BAGBY, GROVER CARLTON · 2002 to 2005
$2.9M
Role of Nucleophosmin in FA-evolved LeukemiaR01CA109641 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI PANG, QISHEN · 2004 to 2008
$1.5M
NCI NIH HHS R01 CA109641NHLBI NIH HHS P01 HL048546NHLBI NIH HHS R01 HL072321NHLBI NIH HHS R01 HL076712
6 · The paper itself

Abstract

Nucleophosmin (NPM) is frequently overexpressed in leukemias and other tumors. NPM has been reported to suppress oncogene-induced senescence and apoptosis and may represent a therapeutic target for cancer. We fused a NPM-derived peptide to the HIV-TAT (TAT-NPMDeltaC) and found that the fusion peptide inhibited proliferation and induced apoptotic death of primary fibroblasts and preleukemic stem cells. TAT-NPMDeltaC down-regulated several NF-kappaB-controlled survival and inflammatory proteins and suppressed NF-kappaB-driven reporter gene activities. Using an inflammation-associated leukemia model, we demonstrate that TAT-NPMDeltaC induced proliferative suppression and apoptosis of preleukemic stem cells and significantly delayed leukemic development in mice. Mechanistically, TAT-NPMDeltaC associated with wild-type NPM proteins and formed complexes with endogenous NPM and p65 at promoters of several antiapoptotic and inflammatory genes and abrogated their transactivation by NF-kappaB in leu-kemic cells. Thus, TAT-delivered NPM peptide may provide a novel therapy for inflammation-associated tumors that require NF-kappaB signaling for survival.

Indexed as

AnimalsApoptosisCell ProliferationDisease Models, AnimalDown-RegulationGene Products, tatInflammationLeukemiaMiceNeoplastic Stem CellsNF-kappa BNuclear ProteinsNucleophosminPeptide FragmentsRecombinant Fusion ProteinsGene Products, tatNF-kappa BNuclear ProteinsNucleophosminPeptide FragmentsRecombinant Fusion Proteins

Identifiers

PMID18574026
PMCPMC2532814
OpenAlexW2051345002

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.