Evidence map›Paper›PMID 19647226›Full record

ArticleCancer cell2009

Tumor suppression by phospholipase C-beta3 via SHP-1-mediated dephosphorylation of Stat5.

Wenbin Xiao, Hong Hong, Yuko Kawakami, Yuko Kato, Dianqing Wu, Hiroki Yasudo, Akiko Kimura, Hiromi Kubagawa, Luigi F Bertoli, Randall S Davis and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 87 citations in OpenAlex.

  1. Phospholipases: Where Do We Stand?Methods in molecular biology (Clifton, N.J.) · 2027
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Phospholipase Signaling in Breast Cancer.Advances in experimental medicine and biology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Protein Tyrosine Phosphatases as Potential Regulators of STAT3 Signaling.International journal of molecular sciences · 2018
    Review
  19. Article
  20. Nuclear phosphoinositide regulation of chromatin.Journal of cellular physiology · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 3 countries.

Wenbin XiaoDivision of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Hong Hong
Yuko Kawakami
Yuko Kato
Dianqing Wu
Hiroki Yasudo
Akiko Kimura
Hiromi Kubagawa
Luigi F Bertoli
Randall S Davis
Luan A Chau
Joaquin Madrenas
Cyrus C Hsia
Anargyros Xenocostas
Thomas J Kipps
Lothar Hennighausen
Atsushi Iwama
Hiromitsu Nakauchi
Toshiaki Kawakami
La Jolla Institute for Immunology · USWestern University · CAChiba University · JPNational Institutes of Health · USUniversity of Alabama at Birmingham · USTokyo University of Science · JPUniversity of California, San Diego · USYale University · US

Funding

Genetic Approaches To Understanding Organ Development and FunctionZIADK061000 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI HENNIGHAUSEN, LOTHAR · 2009 to 2025
$24.7M
Vascular Pathophysiology and History Core (VPHC)P01HL070694 · NHLBI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI COWAN, ANN E. · 2002 to 2013
$17.5M
IgE Regulation of Mast Cell Growth and SurvivalR01AI050209 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KAWAKAMI, TOSHIAKI · 2002 to 2006
$2.3M
Molecular Function of Chemoattractant-Mediated SignalingR01HL080706 · NHLBI · YALE UNIVERSITY · PI WU, DIANQING · 2005 to 2009
$2.3M
Regulation of asthma by Btk and family kinasesR01AI061796 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KAWAKAMI, TOSHIAKI · 2004 to 2008
$2.2M
Therapeutic Targeting of Wnt SignalingR01CA132317 · NCI · YALE UNIVERSITY · PI WU, DIANQING · 2008 to 2012
$1.7M
Functional Role of Fc Receptor Homologs on B Lineage CellsR01AI067467 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVIS, RANDALL S · 2007 to 2011
$1.6M
Molecular Function of Chemoattractant-Mediated SignalingR01GM054597 · NIGMS · UNIVERSITY OF ROCHESTER · PI WU, DIANQING · 1996 to 2004
$1.2M
NCI NIH HHS R01 CA132317NHLBI NIH HHS P01 HL070694NHLBI NIH HHS R01 HL080706NIAID NIH HHS R01 AI050209NIAID NIH HHS R01 AI061796NIAID NIH HHS R01 AI067467NIGMS NIH HHS R01 GM054597
6 · The paper itself

Abstract

Given its catalytic activity to generate diacylglycerol and inositol 1,4,5-trisphosphate, phospholipase C (PLC) is implicated in promoting cell growth. However, we found that PLC-beta3-deficient mice develop myeloproliferative disease, lymphoma, and other tumors. The mutant mice have increased numbers of hematopoietic stem cells with increased proliferative, survival, and myeloid-differentiative abilities. These properties are dependent on Stat5 and can be antagonized by the protein phosphatase SHP-1. Stat5-dependent cooperative transformation by active c-Myc and PLC-beta3 deficiency was suggested in mouse lymphomas in PLC-beta3(-/-) and in Emicro-myc;PLC-beta3(+/-) mice and human Burkitt's lymphoma cells. The same mechanism for malignant transformation seems to be operative in other human lymphoid and myeloid malignancies. Thus, PLC-beta3 is likely a tumor suppressor.

Indexed as

AnimalsCell DifferentiationCell SurvivalCell Transformation, NeoplasticHematopoietic Stem CellsLymphomaMiceMutationMyeloproliferative DisordersPhospholipase C betaPhosphorylationProtein Tyrosine Phosphatase, Non-Receptor Type 6Proto-Oncogene Proteins c-mycSignal TransductionSTAT5 Transcription FactorTumor Suppressor ProteinsPhospholipase C betaProtein Tyrosine Phosphatase, Non-Receptor Type 6Proto-Oncogene Proteins c-mycPtpn6 protein, mouseSTAT5 Transcription FactorTumor Suppressor Proteins

Identifiers

PMID19647226
PMCPMC2744338
OpenAlexW2061855330

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.