Evidence map›Paper›PMID 27027349›Full record

ReviewOncotarget2016

Anticancer properties of nimbolide and pharmacokinetic considerations to accelerate its development.

Lingzhi Wang, Do Dang Khoa Phan, Jingwen Zhang, Pei-Shi Ong, Win Lwin Thuya, Ross Soo, Andrea Li-Ann Wong, Wei Peng Yong, Soo Chin Lee, Paul Chi-Lui Ho and 2 more

Abstract readReview
In one paragraph

Review in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Stereoselective Total Synthesis of Nimbolide.Journal of the American Chemical Society · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Insights into Nimbolide molecular crosstalk and its anticancer properties.Medical oncology (Northwood, London, England) · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Bioinformation · 2022
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Potential of Zerumbone as an Anti-Cancer Agent.Molecules (Basel, Switzerland) · 2019
    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

12 authors.

Lingzhi WangCancer Science Institute of Singapore, National University of Singapore, Singapore.
Do Dang Khoa PhanCancer Science Institute of Singapore, National University of Singapore, Singapore.
Jingwen ZhangDepartment of Pharmacology, National University Health System, Singapore.
Pei-Shi OngDepartment of Pharmacy, National University of Singapore, Singapore.
Win Lwin ThuyaCancer Science Institute of Singapore, National University of Singapore, Singapore.
Ross SooCancer Science Institute of Singapore, National University of Singapore, Singapore.
Andrea Li-Ann WongCancer Science Institute of Singapore, National University of Singapore, Singapore.
Wei Peng YongCancer Science Institute of Singapore, National University of Singapore, Singapore.
Soo Chin LeeCancer Science Institute of Singapore, National University of Singapore, Singapore.
Paul Chi-Lui HoDepartment of Pharmacy, National University of Singapore, Singapore.
Gautam SethiDepartment of Pharmacology, National University Health System, Singapore.
Boon Cher GohCancer Science Institute of Singapore, National University of Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nimbolide is one of the main components in the leaf extract of Azadirachta indica (A. indica). Accumulating evidence from various in vitro and in vivo studies indicates that nimbolide possesses potent anticancer activity against several types of cancer and also shows potential chemopreventive activity in animal models. The main mechanisms of action of nimbolide include anti-proliferation, induction of apoptosis, inhibition of metastasis and angiogenesis, and modulation of carcinogen-metabolizing enzymes. Although multiple pharmacodynamic (PD) studies have been carried out, nimbolide is still at the infant stage in the drug development pipeline due to the lack of systematic pharmacokinetic (PK) studies and long-term toxicological studies. Preclinical PK and toxicological studies are vital in determining the dosage range to support the safety of nimbolide for first-in-human clinical trials. In this review, we will provide a comprehensive summary for the current status of nimbolide as an anticancer and chemopreventive lead compound, and highlight the importance of systematic preclinical PK and toxicological studies in accelerating the process of application of nimbolide as a therapeutic agent against various malignancies.

Indexed as

AnimalsApoptosisAzadirachtaCell ProliferationHumansLimoninsNeoplasmsNeovascularization, PathologicPhytotherapyPlant ExtractsLimoninsnimbolidePlant Extractsanticancer propertynimbolidepharmacodynamicspharmacokineticstoxicology

Identifiers

PMID27027349
PMCPMC5190135

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.