Evidence map›Paper›PMID 21204731›Full record

ReviewExpert opinion on therapeutic targets2011

Targeting NR4A1 (TR3) in cancer cells and tumors.

Syng-Ook Lee, Xi Li, Shaheen Khan, Stephen Safe

Abstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Role of Nuclear Receptors in Controlling Erythropoiesis.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Ethyl Acetate Fraction ofEvidence-based complementary and alternative medicine : eCAM · 2022
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Natural Product Type III Secretion System Inhibitors.Antibiotics (Basel, Switzerland) · 2019
    Review

3 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

4 authors at 2 institutions in 1 country.

Syng-Ook LeeInstitute of Bioscience and Technology, Texas A&M Health Science Center, 2121 W. Holcombe Boulevard, Houston, TX 77030, USA.
Xi Li
Shaheen Khan
Stephen Safe
Texas A&M Health Science Center · USTexas A&M University · US

Funding

NUR77 Agonists: New Targets for Pancreatic Cancer ChemotherapyR01CA124998 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAFE, STEPHEN H. · 2007 to 2011
$1.1M
NCI NIH HHS R01 CA124998PHS HHS R01C124998
6 · The paper itself

Abstract

introductionNuclear receptor 4A1(NR4A1) (testicular receptor 3 (TR3), nuclear hormone receptor (Nur)77) is a member of the nuclear receptor superfamily of transcription factors and is highly expressed in multiple tumor types. RNA interference studies indicate that NR4A1 exhibits growth-promoting, angiogenic and prosurvival activity in most cancers. AREAS COVERED: Studies on several apoptosis-inducing agents that activate nuclear export of NR4A1, which subsequently forms a mitochondrial NR4A1-bcl-2 complex that induces the intrinsic pathway for apoptosis are discussed. Cytosporone B and related compounds that induce NR4A1-dependent apoptosis in cancer cells through both modulation of nuclear NR4A1 and nuclear export are discussed. A relatively new class of diindolylmethane analogs (C-DIMs) including 1,1-bis(3'-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) (NR4A1 activator) and 1,1-bis(3'-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) (NR4A1 deactivator) are discussed in more detail. These anticancer drugs (C-DIMs) act strictly through nuclear NR4A1 and induce apoptosis in cancer cells and tumors. EXPERT OPINION: It is clear that NR4A1 plays an important pro-oncogenic role in cancer cells and tumors, and there is increasing evidence that this receptor can be targeted by anticancer drugs that induce cell death via NR4A1-dependent and -independent pathways. Since many of these compounds exhibit relatively low toxicity, they represent an important class of mechanism-based anticancer drugs with excellent potential for clinical applications.

Indexed as

Molecular Targeted TherapyActive Transport, Cell NucleusAnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell NucleusHumansIndolesMiceNeoplasmsNuclear Receptor Subfamily 4, Group A, Member 1PhenolsPhenylacetatesRNA Interference1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methaneAntineoplastic Agentscytosporone BIndolesNuclear Receptor Subfamily 4, Group A, Member 1PhenolsPhenylacetates

Identifiers

PMID21204731
PMCPMC4407471
OpenAlexW2120386878

What OpenQuestion holds

Textmetadata
LicenceTDM
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.