Evidence map›Paper›PMID 19666870›Full record

ArticleBlood2010

The cytoplasmic NPM mutant induces myeloproliferation in a transgenic mouse model.

Ke Cheng, Paolo Sportoletti, Keisuke Ito, John G Clohessy, Julie Teruya-Feldstein, Jeffery L Kutok, Pier Paolo Pandolfi

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

56 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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  6. Article
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  8. Article
  9. Review
  10. Article
  11. Murine Models of Acute Myeloid Leukemia.Frontiers in oncology · 2022
    Review
  12. Review
  13. Mouse Models of Myeloid Malignancies.Cold Spring Harbor perspectives in medicine · 2021
    Review
  14. International journal of molecular sciences · 2020
    Review
  15. Article
  16. NPM1 Biology in Myeloid Neoplasia.Current hematologic malignancy reports · 2020
    Review
  17. Article
  18. Review
  19. Review
  20. 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

7 authors at 4 institutions in 1 country.

Ke ChengCancer Genetics Program, Beth Israel Deaconess Cancer Center and Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Paolo Sportoletti
Keisuke Ito
John G Clohessy
Julie Teruya-Feldstein
Jeffery L Kutok
Pier Paolo Pandolfi
Cancer Genetics (United States) · USBeth Israel Deaconess Medical Center · USBrigham and Women's Hospital · USMemorial Sloan Kettering Cancer Center · US

Funding

FUSION PROTEINS IN THE MOLECULAR PATHOGENESIS OF APLR01CA074031 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PANDOLFI, PIER PAOLO · 1997 to 2009
$3.8M
X-RAR alpha proteins: Molecualr Pathogenesis of Acute Promyelocytic LeukemiaR37CA071692 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI PANDOLFI, PIER PAOLO · 2006 to 2010
$1.8M
PML, PLZF, NPM AND NUMA IN THE PATHOGENESIS OF APLR01CA071692 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PANDOLFI, PIER PAOLO · 1996 to 2005
$1.8M
NCI NIH HHS CA-71692NCI NIH HHS CA-74031NCI NIH HHS R01 CA071692NCI NIH HHS R01 CA074031NCI NIH HHS R37 CA071692
6 · The paper itself

Abstract

Although NPM1 gene mutations leading to aberrant cytoplasmic expression of nucleophosmin (NPMc(+)) are the most frequent genetic lesions in acute myeloid leukemia, there is yet no experimental model demonstrating their oncogenicity in vivo. We report the generation and characterization of a transgenic mouse model expressing the most frequent human NPMc(+) mutation driven by the myeloid-specific human MRP8 promoter (hMRP8-NPMc(+)). In parallel, we generated a similar wild-type NPM trans-genic model (hMRP8-NPM). Interestingly, hMRP8-NPMc(+) transgenic mice developed myeloproliferation in bone marrow and spleen, whereas nontransgenic littermates and hMRP8-NPM transgenic mice remained disease free. These findings provide the first in vivo evidence indicating that NPMc(+) confers a proliferative advantage in the myeloid lineage. No spontaneous acute myeloid leukemia was found in hMPR8-NPMc(+) or hMRP8-NPM mice. This model will also aid in the development of therapeutic regimens that specifically target NPMc(+).

Indexed as

Gene Expression Regulation, LeukemicAnimalsBlotting, WesternCell SeparationCytoplasmDisease Models, AnimalFlow CytometryHumansLeukemia, Myeloid, AcuteMiceMice, Inbred C57BLMice, Inbred CBAMice, TransgenicMutationMyeloid CellsNuclear ProteinsNPM1 protein, humanNpm1 protein, mouseNuclear ProteinsNucleophosmin

Identifiers

PMID19666870
PMCPMC2858489
OpenAlexW2021142476

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.