Evidence map›Paper›PMID 27100893›Full record

ReviewCell death & disease2016

Cell cycle and apoptosis regulation by NFAT transcription factors: new roles for an old player.

G P Mognol, F R G Carneiro, B K Robbs, D V Faget, J P B Viola

Abstract readReview
In one paragraph

Review in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
–field-weighted citation impact
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

125 citing papers in PubMed.

  1. Article
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  4. metileneNature communications · 2026
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65 more citing papers are in PubMed but not listed here.

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

5 authors.

G P MognolPrograma de Biologia Celular, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
F R G CarneiroLaboratory for Proteomics and Protein Engineering, Carlos Chagas Institute, FIOCRUZ-Paraná, Brazil.
B K RobbsDepartment of Basic Sciences (FCB), Universidade Federal Fluminense, Nova Friburgo, Brazil.
D V FagetPrograma de Biologia Celular, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
J P B ViolaPrograma de Biologia Celular, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The NFAT (nuclear factor of activated T cells) family of transcription factors consists of four Ca(2+)-regulated members (NFAT1-NFAT4), which were first described in T lymphocytes. In addition to their well-documented role in T lymphocytes, where they control gene expression during cell activation and differentiation, NFAT proteins are also expressed in a wide range of cells and tissue types and regulate genes involved in cell cycle, apoptosis, angiogenesis and metastasis. The NFAT proteins share a highly conserved DNA-binding domain (DBD), which allows all NFAT members to bind to the same DNA sequence in enhancers or promoter regions. The same DNA-binding specificity suggests redundant roles for the NFAT proteins, which is true during the regulation of some genes such as IL-2 and p21. However, it has become increasingly clear that different NFAT proteins and even isoforms can have unique functions. In this review, we address the possible reasons for these distinct roles, particularly regarding N- and C-terminal transactivation regions (TADs) and the partner proteins that interact with these TADs. We also discuss the genes regulated by NFAT during cell cycle regulation and apoptosis and the role of NFAT during tumorigenesis.

Indexed as

ApoptosisCASP8 and FADD-Like Apoptosis Regulating ProteinCell Cycle CheckpointsCell Transformation, NeoplasticFas Ligand ProteinHumansMEF2 Transcription FactorsNFATC Transcription FactorsNuclear Proteinsp300-CBP Transcription FactorsReceptors, EstrogenCASP8 and FADD-Like Apoptosis Regulating ProteinFas Ligand ProteinMEF2 Transcription FactorsNFATC Transcription FactorsNuclear Proteinsp300-CBP Transcription FactorsReceptors, Estrogen

Identifiers

PMID27100893
PMCPMC4855676

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.