Evidence map›Paper›PMID 16606833›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Identification of small molecules that induce apoptosis in a Myc-dependent manner and inhibit Myc-driven transformation.

Hao Mo, Marie Henriksson

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
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  6. Review
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  9. Article
  10. Review
  11. MYC inhibitors in multiple myeloma.Cancer drug resistance (Alhambra, Calif.) · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. The role of c-Myc-RBM38 loop in the growth suppression in breast cancer.Journal of experimental & clinical cancer research : CR · 2017
    Article
  18. Review
  19. Article
  20. Strategies to Inhibit Myc and Their Clinical Applicability.Frontiers in cell and developmental biology · 2017
    Review
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

2 authors at 1 institution in 1 country.

Hao MoMicrobiology and Tumor Biology Center, Karolinska Institutet, S-171 77 Stockholm, Sweden.
Marie Henriksson
Karolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Myc transcription factor plays a central role in the regulation of cell cycle progression, apoptosis, angiogenesis, and cellular transformation. Myc is a potent oncoprotein that is deregulated in a wide variety of human tumors and is therefore an attractive target for novel cancer therapies. Using a cellular screening approach, we have identified low-molecular-weight compounds, Myc pathway response agents (MYRAs), that induce apoptosis in a c-Myc-dependent manner and inhibit Myc-driven cellular transformation. MYRA-A inhibits Myc transactivation and interferes with the DNA-binding activity of Myc family proteins but has no effect on the E-box-binding protein USF. In contrast, MYRA-B induces Myc-dependent apoptosis without affecting Myc transactivation or Myc/Max DNA binding. Our data show that cellular screening assays can be a powerful strategy for the identification of candidate substances that modulate the Myc pathway. These compounds can be useful tools for studying Myc function and may also be of therapeutic potential as leads for drug development.

Indexed as

ApoptosisDrug Screening Assays, AntitumorAnimalsAnthracenesAntineoplastic AgentsCell Transformation, NeoplasticDiaminesDNAHumansHydrazonesProto-Oncogene Proteins c-mycPurinesRatsTranscriptional ActivationTranscription FactorsAnthracenesAntineoplastic AgentsDiaminesDNAHydrazonesMYC protein, humanNSC 339585NSC 45641Proto-Oncogene Proteins c-mycPurinesTranscription Factors

Identifiers

PMID16606833
PMCPMC1435363
OpenAlexW2149172695

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.