Evidence map›Paper›PMID 14982843›Full record

ArticleThe American journal of pathology2004

An anti-apoptotic role for galectin-3 in diffuse large B-cell lymphomas.

Katrina K Hoyer, Mabel Pang, Dorina Gui, I Peter Shintaku, Ichiro Kuwabara, Fu-Tong Liu, Jonathan W Said, Linda G Baum, Michael A Teitell

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

48 citing papers in PubMed, 119 citations in OpenAlex.

  1. Review
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  9. Human umbilical cord mesenchymal stem cell-derived exosomes carrying hsa-miRNA-128-3p suppress pancreatic ductal cell carcinoma by inhibiting Galectin-3.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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  12. Analysis of Galectin-Binding Receptors on B Cells.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
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  15. A Chimeric Signal Peptide-Galectin-3 Conjugate Induces Glycosylation-Dependent Cancer Cell-Specific Apoptosis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
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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

9 authors at 2 institutions in 1 country.

Katrina K HoyerDepartment of Pathology and Laboratory Medicine, University of California at Los Angeles School of Medicine, Los Angeles, California 90095-1732, USA.
Mabel Pang
Dorina Gui
I Peter Shintaku
Ichiro Kuwabara
Fu-Tong Liu
Jonathan W Said
Linda G Baum
Michael A Teitell
University of California, Los Angeles · USUniversity of California, Davis · US

Funding

TCL1 ONCOGENE IN B LYMPHOCYTE DEVELOPMENT AND NEOPLASIAR01CA090571 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TEITELL, MICHAEL A · 2002 to 2015
$3.8M
IGE BINDING PROTEIN--A MULTIFUNCTIONAL ANIMAL LECTINR01AI020958 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI LIU, FU-TONG · 1985 to 2008
$2.0M
A NOVEL MECHANISM OF TCL1 TUMORIGENESISR01CA107300 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TEITELL, MICHAEL A · 2004 to 2008
$1.4M
GALECTINS IN ALLERGIC INFLAMMATIONR01AI039620 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI LIU, FU-TONG · 1997 to 2005
$1.2M
A Novel Cell Death Pathway Induced by Galectin-1R01GM063281 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BAUM, LINDA G · 2001 to 2004
$1.0M
NCI NIH HHS CA107300NCI NIH HHS CA90571NCI NIH HHS R01 CA090571NCI NIH HHS R01 CA107300NCI NIH HHS T32CA090056NIAID NIH HHS AI20958NIAID NIH HHS AI39620NIAID NIH HHS R01 AI020958NIAID NIH HHS R01 AI039620NIGMS NIH HHS GM63281NIGMS NIH HHS R01 GM063281
6 · The paper itself

Abstract

Increased resistance to apoptosis promotes lymphomagenesis with aberrant expression of cell survival proteins such as BCL-2 and c-MYC occurring in distinct lymphoma subtypes. Galectin-3 is an anti-apoptotic protein that protects T cells, macrophages, and breast carcinoma cells from death triggered by a variety of agents. We have found high levels of galectin-3 protein expression in a subset of B-cell neoplasms including diffuse large B-cell lymphoma (DLBCL), primary effusion lymphoma (PEL), and multiple myeloma (MM), in both cell lines and patient samples. However, we failed to detect galectin-3 in Burkitt lymphoma (BL), follicular lymphoma (FL), marginal zone lymphoma (MZL), MALT lymphoma or B-small lymphocytic lymphoma (B-SLL) cell lines or patient samples. To determine whether galectin-3 expression protects B cells from apoptosis, galectin-3-negative BL cells were transfected with a galectin-3 expressing plasmid, which resulted in markedly increased resistance to anti-Fas-induced cell death. In contrast, galectin-3-positive PEL cells transfected with an amino-terminal truncated galectin-3 vector showed increased sensitivity to anti-Fas induced apoptosis. During normal B-cell development, galectin-3 expression was lowest in germinal center and plasma B cells, from which DLBCL, PEL, and MM derive, and highest in long-lived naïve and memory B cells. This pattern of expression suggests that aberrantly increased galectin-3 levels in specific B-cell populations may yield a protective advantage during transformation and/or progression of certain B-cell neoplasms.

Indexed as

AnimalsApoptosisBlotting, WesternB-LymphocytesCell Line, TransformedCell Line, TumorEpstein-Barr Virus InfectionsGalectin 3Gene Expression Regulation, NeoplasticGenes, mycHumansLymphoma, B-CellLymphoma, Large B-Cell, DiffuseTransfectionGalectin 3

Identifiers

PMID14982843
PMCPMC1614710
OpenAlexW2100115439

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.