Evidence map›Paper›PMID 16007226›Full record

ArticleOncogene2005

Inhibition of Wnt16 in human acute lymphoblastoid leukemia cells containing the t(1;19) translocation induces apoptosis.

Julien Mazieres, Liang You, Biao He, Zhidong Xu, Amie Y Lee, Iwao Mikami, Frank McCormick, David M Jablons

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.3field-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

54 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
  2. Article
  3. Wnt regulation of hematopoietic stem cell development and disease.Current topics in developmental biology · 2023
    Review
  4. Review
  5. Article
  6. WNT Signalling in Osteoarthritis and Its Pharmacological Targeting.Handbook of experimental pharmacology · 2021
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Wnt Signaling in Hematological Malignancies.Progress in molecular biology and translational science · 2018
    Review
  18. Review
  19. Review
  20. Wnt Signaling: Role in Regulation of Haematopoiesis.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2016
    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

8 authors at 1 institution in 1 country.

Julien MazieresUCSF Comprehensive Cancer Center, San Francisco, CA 94115, USA.
Liang You
Biao He
Zhidong Xu
Amie Y Lee
Iwao Mikami
Frank McCormick
David M Jablons
UCSF Helen Diller Family Comprehensive Cancer Center · US

Funding

The Wnt Pathway in Malignant MesotheliomaR01CA093708 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JABLONS, DAVID M. · 2005 to 2008
$883k
NCI NIH HHS R01 CA093708
6 · The paper itself

Abstract

The Wnt family of secreted glycoproteins is widely involved in cell proliferation, differentiation and oncogenesis. Many Wnt signaling genes are upregulated and activated in chronic lymphocytic leukemia. Less is known concerning acute leukemia. One subtype of acute lymphoblastoid leukemia (ALL) is characterized by a t(1;19) chromosomal translocation resulting in a fusion protein E2A-Pbx1 that promotes transformation and leukemogenesis. Wnt16 has been shown to be targeted by E2A-Pbx1. We performed a differential gene expression array in acute leukemia cell lines displaying or not displaying the t(1;19) translocation. We found that Wnt16 and many Wnt signaling-related genes were upregulated in the translocation-containing cells. As two isoforms of Wnt16, Wnt16a and Wnt16b, have been recently identified, we demonstrated by using RT-PCR and Western blot that Wnt16b (and not Wnt16a) is overexpressed in t(1;19)-containing cell lines. We then directly addressed the role played by both isoforms in this type of leukemia. Using specific short interfering RNA (siRNA) and an anti-Wnt16 antibody, we showed that targeted-Wnt16b inhibition leads to apoptotic cell death. We also demonstrated that Wnt16b mediates its effect through the canonical Wnt pathway involving dishevelled-2, beta-catenin and survivin. We thus propose that Wnt16 plays an important role in leukemogenesis, raising its therapeutic interest.

Indexed as

Chromosomes, Human, Pair 1Chromosomes, Human, Pair 19Translocation, GeneticApoptosisGene Expression ProfilingGlycoproteinsHumansPrecursor Cell Lymphoblastic Leukemia-LymphomaReverse Transcriptase Polymerase Chain ReactionRNA, Small InterferingTumor Cells, CulturedUp-RegulationWnt ProteinsGlycoproteinsRNA, Small InterferingWNT16 protein, humanWnt Proteins

Identifiers

PMID16007226
OpenAlexW2067449053

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.