Evidence map›Paper›PMID 20882051›Full record

ArticleLeukemia2010

Overexpression of survivin initiates hematologic malignancies in vivo.

S Small, G Keerthivasan, Z Huang, S Gurbuxani, J D Crispino

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 61 citations in OpenAlex.

  1. TheInternational journal of molecular sciences · 2021
    Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. The Triple Crown: NO, CO, and HPharmacology & therapeutics · 2023
    Review
  7. CBX5 loss drives EGFR inhibitor resistance and results in therapeutically actionable vulnerabilities in lung cancer.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Dual role of deubiquitinating enzyme USP19 regulates mitotic progression and tumorigenesis by stabilizing survivin.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Survivin - The inconvenient IAP.Seminars in cell & developmental biology · 2015
    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.

S SmallDivision of Hematology and Oncology, Northwestern University Chicago, Chicago, IL 60611, USA.
G Keerthivasan
Z Huang
S Gurbuxani
J D Crispino
Northwestern University · USUniversity of Chicago · US

Funding

Role of Survivin in Development of Megakaryocytes and Erythroid CellsR01DK074693 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CRISPINO, JOHN D · 2007 to 2011
$1.6M
Mechanisms of erythroblast enucleationR56DK074693 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CRISPINO, JOHN D · 2012 to 2012
$139k
NIDDK NIH HHS DK074693NIDDK NIH HHS R01 DK074693NIDDK NIH HHS R56 DK074693
6 · The paper itself

Abstract

Survivin is an inhibitor of apoptosis protein family member that has an essential role in cellular proliferation as a component of the chromosome passenger complex. Survivin is highly expressed in embryos and in proliferating adult tissues, but it is not expressed in most differentiated cells. During tumorigenesis, however, survivin expression is dramatically upregulated. Although many studies have shown that survivin is required for cancer cells, the extent to which survivin contributes to the initiation of tumors is unknown. Here we show that transgenic mice that overexpress survivin in hematopoietic cells are at an increased risk of hematologic tumors. In examining how survivin might contribute to tumorigenesis, we observed that hematopoietic cells engineered to overexpress survivin are less susceptible to apoptosis. We conclude that survivin may promote tumorigenesis by imparting a survival advantage to cells that acquire additional genetic lesions.

Indexed as

Up-RegulationAnimalsApoptosisCell DifferentiationCell SurvivalFlow CytometryGATA1 Transcription FactorGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHematologic NeoplasmsHematopoietic Stem CellsHumansInhibitor of Apoptosis ProteinsMiceMice, Inbred BALB CMicrotubule-Associated ProteinsBIRC5 protein, humanGata1 protein, mouseGATA1 Transcription FactorInhibitor of Apoptosis ProteinsMicrotubule-Associated ProteinsNeoplasm ProteinsSurvivin

Identifiers

PMID20882051
PMCPMC2978276
OpenAlexW2063512039

What OpenQuestion holds

Textmetadata
LicenceTDM
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.