Evidence map›Paper›PMID 26517933›Full record

ReviewBiochemical Society transactions2015

Tribbles in normal and malignant haematopoiesis.

Sarah J Stein, Ethan A Mack, Kelly S Rome, Warren S Pear

Open access · bronzeAbstract readReview
In one paragraph

Review in Biochemical Society transactions, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. The role of tribbles homolog 2 in cell proliferation.Cell communication and signaling : CCS · 2025
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  18. DoIn vivo (Athens, Greece)
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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

4 authors at 1 institution in 1 country.

Sarah J SteinDepartment of Pathology and Laboratory Medicine, Institute for Immunology, Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, U.S.A.
Ethan A MackDepartment of Pathology and Laboratory Medicine, Institute for Immunology, Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, U.S.A.
Kelly S RomeDepartment of Pathology and Laboratory Medicine, Institute for Immunology, Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, U.S.A.
Warren S PearDepartment of Pathology and Laboratory Medicine, Institute for Immunology, Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, U.S.A. wpear@mail.med.upenn.edu.
Parker Institute for Cancer Immunotherapy · US

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
Notch Regulation of Hematopoietic Cell FatesR01AI047833 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI JORDAN, MARTHA S, PEAR, WARREN S · 2000 to 2022
$7.4M
Trib1 in NF-kappaB Signaling: Insights into MALT1 Regulation and LeukemiaF31CA189661 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROME, KELLY · 2014 to 2016
$116k
NCI NIH HHS F31CA189661NCI NIH HHS T32 CA009140NHLBI NIH HHS T32 HL0074NIAID NIH HHS R01 AI047833NIGMS NIH HHS T32 GM0071
6 · The paper itself

Abstract

The tribbles protein family, an evolutionarily conserved group of pseudokinases, have been shown to regulate multiple cellular events including those involved in normal and malignant haematopoiesis. The three mammalian Tribbles homologues, Trib1, Trib2 and Trib3 are characterized by conserved motifs, including a pseudokinase domain and a C-terminal E3 ligase-binding domain. In this review, we focus on the role of Trib (mammalian Tribbles homologues) proteins in mammalian haematopoiesis and leukaemia. The Trib proteins show divergent expression in haematopoietic cells, probably indicating cell-specific functions. The roles of the Trib proteins in oncogenesis are also varied and appear to be tissue-specific. Finally, we discuss the potential mechanisms by which the Trib proteins preferentially regulate these processes in multiple cell types.

Indexed as

Acute DiseaseAnimalsCalcium-Calmodulin-Dependent Protein KinasesGene Expression Regulation, LeukemicHematopoiesisHumansIntracellular Signaling Peptides and ProteinsLeukemia, MyeloidModels, GeneticProtein Serine-Threonine KinasesSignal TransductionCalcium-Calmodulin-Dependent Protein KinasesIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesTRIB1 protein, humanTRIB2 protein, humanhaematopoiesisleukaemiatribbles

Identifiers

PMID26517933
PMCPMC4613494
OpenAlexW2346269401

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.