Evidence map›Paper›PMID 24486850›Full record

ReviewCancer letters2014

Oleanolic acid and its synthetic derivatives for the prevention and therapy of cancer: preclinical and clinical evidence.

Muthu K Shanmugam, Xiaoyun Dai, Alan Prem Kumar, Benny K H Tan, Gautam Sethi, Anupam Bishayee

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
11.1field-weighted citation impact, top 1% 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

93 citing papers in PubMed, 262 citations in OpenAlex.

  1. Review
  2. Article
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  8. Article
  9. Article
  10. Article
  11. Anti-cancer agents in medicinal chemistry · 2025
    Article
  12. Article
  13. Review
  14. Therapeutic potential of oleanolic acid in liver diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Review
  15. Article
  16. Review
  17. Review
  18. Anti-Tumor Effects and Toxicity Reduction Mechanisms ofMolecules (Basel, Switzerland) · 2024
    Review
  19. Review
  20. Article

33 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

6 authors at 4 institutions in 3 countries.

Muthu K ShanmugamDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Xiaoyun DaiDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Alan Prem KumarDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Cancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore; School of Biomedical Sciences, Faculty of Health Sciences, Curtin University, Western Australia, Australia; Department of Biological Sciences, University of North Texas, Denton, TX, USA.
Benny K H TanDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Gautam SethiDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Cancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore. Electronic address: phcgs@nus.edu.sg.
Anupam BishayeeDepartment of Pharmaceutical Sciences, School of Pharmacy, American University of Health Sciences, Signal Hill, CA, USA. Electronic address: abishayee@auhs.edu.
National University of Singapore · SGAmerican University of Health Sciences · USNational University Cancer Institute, Singapore · SGUniversity of North Texas · US

Funding

A synthetic triterpenoid in breast cancer chemopreventionR03CA136014 · NCI · NORTHEAST OHIO MEDICAL UNIVERSITY · PI BISHAYEE, ANUPAM · 2009 to 2010
$154k
NCI NIH HHS R03 CA136014NCI NIH HHS R03CA136014
6 · The paper itself

Abstract

Oleanolic acid (OA, 3β-hydroxyolean-12-en-28-oic acid) is a ubiquitous pentacyclic multifunctional triterpenoid, widely found in several dietary and medicinal plants. Natural and synthetic OA derivatives can modulate multiple signaling pathways including nuclear factor-κB, AKT, signal transducer and activator of transcription 3, mammalian target of rapamycin, caspases, intercellular adhesion molecule 1, vascular endothelial growth factor, and poly (ADP-ribose) polymerase in a variety of tumor cells. Importantly, synthetic derivative of OA, 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid (CDDO), and its C-28 methyl ester (CDDO-Me) and C28 imidazole (CDDO-Im) have demonstrated potent antiangiogenic and antitumor activities in rodent cancer models. These agents are presently under evaluation in phase I studies in cancer patients. This review summarizes the diverse molecular targets of OA and its derivatives and also provides clear evidence on their promising potential in preclinical and clinical situations.

Indexed as

AnimalsClinical Trials, Phase I as TopicHumansNeoplasmsTriterpenesoleanonic acidTriterpenesCDDOInflammation cancerOleanolic acidPentacyclic triterpenoidsSynthetic triterpenoids

Identifiers

PMID24486850
PMCPMC4004441
OpenAlexW1997470573

What OpenQuestion holds

Textmetadata
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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.