Evidence map›Paper›PMID 19430495›Full record

ArticleOncogene2009

Gene deletion of inositol hexakisphosphate kinase 2 predisposes to aerodigestive tract carcinoma.

B H Morrison, R Haney, E Lamarre, J Drazba, G D Prestwich, D J Lindner

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

45 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. The Inositol Phosphate System-A Coordinator of Metabolic Adaptability.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Inositol hexakisphosphate kinase-2 determines cellular energy dynamics by regulating creatine kinase-B.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. The Key Role of IPMolecules (Basel, Switzerland) · 2020
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Inositol hexakisphosphate kinase 3 promotes focal adhesion turnover via interactions with dynein intermediate chain 2.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. The inositol pyrophosphate pathway in health and diseases.Biological reviews of the Cambridge Philosophical Society · 2018
    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

6 authors at 3 institutions in 1 country.

B H MorrisonDepartment of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
R Haney
E Lamarre
J Drazba
G D Prestwich
D J Lindner
Cleveland Clinic · USCleveland Clinic Lerner College of Medicine · USUniversity of Utah · US

Funding

Phosphoinositide and Inositol Polyphosphate ProbesR01NS029632 · NINDS · UNIVERSITY OF UTAH · PI PRESTWICH, GLENN DOWNES · 1992 to 2007
$2.5M
Inositol hexakisphosphate kinase 2:apoptosis regulatorR01CA095020 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LINDNER, DANIEL J · 2003 to 2006
$1.1M
NCI NIH HHS CA095020NCI NIH HHS R01 CA095020NINDS NIH HHS NS29632NINDS NIH HHS R01 NS029632
6 · The paper itself

Abstract

Inositol hexakisphosphate kinase 2 (IP6K2), a member of the inositol hexakisphosphate kinase family, functions as a growth suppressive and apoptosis-enhancing kinase during cell stress. We created mice with a targeted deletion of IP6K2; these mice display normal embryogenesis, development, growth and fertility. Chronic exposure to the carcinogen 4-nitroquinoline 1-oxide (4-NQO, a UV-mimetic compound) in drinking water resulted in fourfold increased incidence of invasive squamous cell carcinoma (SCC) formation in the oral cavity and esophagus of the knockout (KO) mice compared to the wild-type (WT) littermates. Paradoxically, KO mice displayed relative resistance to ionizing radiation and exhibit enhanced survival following 8-10 Gy total body irradiation. Primary KO fibroblasts displayed resistance to antiproliferative effects of interferon-beta and increased colony forming units following ionizing radiation. Radioresistance of KO fibroblasts was associated with accelerated DNA repair measured by comet assay. Direct microinjection of 5-PP-Ins(1,2,3,4,6)P(5) (the enzymatic product of IP6K2), but not InsP(6) (the substrate of IP6K2) induced cell death in SCC22A squamous carcinoma cells.

Indexed as

Gene Deletion4-Nitroquinoline-1-oxideAnimalsApoptosisCarcinogensCarcinoma, Squamous CellEsophageal NeoplasmsFemaleFibroblastsGamma RaysGene Expression ProfilingGenetic Predisposition to DiseaseImmunoblottingMaleMiceMice, Inbred C57BL4-Nitroquinoline-1-oxideCarcinogensinositol hexakisphosphate kinasePhosphotransferases (Phosphate Group Acceptor)

Identifiers

PMID19430495
PMCPMC3171149
OpenAlexW2068361003

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.