Evidence map›Paper›PMID 24394940›Full record

ReviewCell cycle (Georgetown, Tex.)2014

c-MYC-miRNA circuitry: a central regulator of aggressive B-cell malignancies.

Jiangchuan Tao, Xiaohong Zhao, Jianguo Tao

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. microRNA Profile of High-Grade B-Cell Lymphoma with 11q Aberration.International journal of molecular sciences · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Cross-talk between Myc and p53 in B-cell lymphomas.Chronic diseases and translational medicine · 2019
    Article
  17. c-Myc is a novelThe Journal of biological chemistry · 2018
    Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Jiangchuan TaoDepartments of Hematopathology and Laboratory Medicine; H Lee Moffitt Cancer Center and Research Institute at the University of South Florida; Tampa, FL USA.
Xiaohong ZhaoDepartments of Hematopathology and Laboratory Medicine; H Lee Moffitt Cancer Center and Research Institute at the University of South Florida; Tampa, FL USA.
Jianguo TaoDepartments of Hematopathology and Laboratory Medicine; H Lee Moffitt Cancer Center and Research Institute at the University of South Florida; Tampa, FL USA.
University of Tampa · US

Funding

Tageting BAFF and BAFF-Induced Non-Canonical NF-kB Pathways for Enhancing Mantle R01CA137123 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI TAO, JIANGUO · 2009 to 2013
$1.3M
NCI NIH HHS R01 CA137123
6 · The paper itself

Abstract

MYC (c-Myc) deregulation has been frequently associated with aggressive lymphomas and adverse clinical outcome in B-cell malignancies. MYC has been implicated in controlling the expression of miRNAs, and MYC-regulated miRNAs affect virtually all aspects of the hallmarks of MYC-driven lymphomas. Increasing evidence has indicated that there is significant cross-talk between MYC and miRNAs, with MYC regulating expression of a number of miRNAs, resulting in widespread repression of miRNA and, at the same time, MYC being subjected to regulation by miRNAs, leading to sustained MYC activity and the corresponding MYC downstream pathways. Thus, these combined effects of MYC overexpression and downregulation of miRNAs play a central regulatory role in the MYC oncogenic pathways and MYC-driven lymphomagenesis. Here, we provide biological insight on the function of MYC-regulated miRNAs, the mechanisms of MYC-induced miRNA repression, and the complicated feedback circuitry underlying lymphoma progression, as well as potential therapeutic targets in aggressive B-cell lymphomas.

Indexed as

AnimalsAntineoplastic AgentsDrug Resistance, NeoplasmHumansLymphoma, B-CellMiceMicroRNAsNeoplasm InvasivenessNeoplastic Stem CellsProto-Oncogene Proteins c-mycAntineoplastic AgentsMicroRNAsMYC protein, humanProto-Oncogene Proteins c-mycaggressive B-cell lymphomasc-MYCepigeneticmethylationmiRNA

Identifiers

PMID24394940
PMCPMC3906236
OpenAlexW1998413047

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.