Evidence map›Paper›PMID 27399331›Full record

ArticleCell cycle (Georgetown, Tex.)2016

NFAT1 transcription factor regulates cell cycle progression and cyclin E expression in B lymphocytes.

Leonardo K Teixeira, Nina Carrossini, Cristiane Sécca, José E Kroll, Déborah C DaCunha, Douglas V Faget, Lilian D S Carvalho, Sandro J de Souza, João P B Viola

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.3field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. RNA Helicases as Shadow Modulators of Cell Cycle Progression.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Characterizing diversity in the tumor-immune microenvironment of distinct subclasses of gastroesophageal adenocarcinomas.Annals of oncology : official journal of the European Society for Medical Oncology · 2020
    Article
  14. Article
  15. Article
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.

Leonardo K Teixeiraa Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
Nina Carrossinia Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
Cristiane Séccaa Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
José E Krollb Brain Institute, Federal University of Rio Grande do Norte (UFRN) , Natal , Brazil.
Déborah C DaCunhaa Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
Douglas V Fageta Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
Lilian D S Carvalhoa Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
Sandro J de Souzab Brain Institute, Federal University of Rio Grande do Norte (UFRN) , Natal , Brazil.
João P B Violaa Program of Cellular Biology , Brazilian National Cancer Institute (INCA) , Rio de Janeiro , Brazil.
Instituto Nacional do Câncer · BRUniversidade Federal do Rio Grande do Norte · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The NFAT family of transcription factors has been primarily related to T cell development, activation, and differentiation. Further studies have shown that these ubiquitous proteins are observed in many cell types inside and outside the immune system, and are involved in several biological processes, including tumor growth, angiogenesis, and invasiveness. However, the specific role of the NFAT1 family member in naive B cell proliferation remains elusive. Here, we demonstrate that NFAT1 transcription factor controls Cyclin E expression, cell proliferation, and tumor growth in vivo. Specifically, we show that inducible expression of NFAT1 inhibits cell cycle progression, reduces colony formation, and controls tumor growth in nude mice. We also demonstrate that NFAT1-deficient naive B lymphocytes show a hyperproliferative phenotype and high levels of Cyclin E1 and E2 upon BCR stimulation when compared to wild-type B lymphocytes. NFAT1 transcription factor directly regulates Cyclin E expression in B cells, inhibiting the G1/S cell cycle phase transition. Bioinformatics analysis indicates that low levels of NFAT1 correlate with high expression of Cyclin E1 in different human cancers, including Diffuse Large B-cell Lymphomas (DLBCL). Together, our results demonstrate a repressor role for NFAT1 in cell cycle progression and Cyclin E expression in B lymphocytes, and suggest a potential function for NFAT1 protein in B cell malignancies.

Indexed as

Cell CycleAnimalsB-LymphocytesCell Cycle CheckpointsCell ProliferationCHO CellsCricetinaeCricetulusCyclin EHumansJurkat CellsLymphoma, B-CellMice, Inbred BALB CMice, NudeNFATC Transcription FactorsPromoter Regions, GeneticCyclin ENFATC Transcription FactorsB lymphocytescell cyclecyclin ENFATTumor

Identifiers

PMID27399331
PMCPMC5004684
OpenAlexW2462554863

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.