Evidence map›Paper›PMID 34896543›Full record

ReviewPharmacological research2022

The purple mangosteen (Garcinia mangostana): Defining the anticancer potential of selected xanthones.

Mirielle C Nauman, Jeremy J Johnson

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacological research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
11.1field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Therapeutic Potential of Plant Phenolic Acids Combating Cancer Drug Resistance.Recent advances in food, nutrition & agriculture · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Endothelial-Protective Actions of Diethylether Extract fromInternational journal of molecular sciences · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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.

Mirielle C NaumanUniversity of Illinois at Chicago, College of Pharmacy, Department of Pharmacy Practice, USA.
Jeremy J JohnsonUniversity of Illinois at Chicago, College of Pharmacy, Department of Pharmacy Practice, USA. Electronic address: jjjohn@uic.edu.
University of Illinois Chicago · US

Funding

UIC CANCER PREVENTION &CONTROL RESEARCH TRAINING GRANTR25CA057699 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FITZGIBBON, MARIAN L. · 1992 to 2017
$8.2M
Cancer Health Equity Career Development ProgramT32CA057699 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Marian L. Fitzgibbon · 2018 to 2026
$3.0M
Defining the role of isoprenylated xanthones from the mangosteen for enhancing degradation of full length and variant forms of androgen receptor in prostate cancerR37CA227101 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI JOHNSON, JEREMY JAMES · 2019 to 2025
$2.5M
NCI NIH HHS R25 CA057699NCI NIH HHS R37 CA227101NCI NIH HHS T32 CA057699
6 · The paper itself

Abstract

The purple mangosteen (Garcinia mangostana) is a popular Southeast Asian fruit that has been used traditionally for its health promoting benefits for years. Unique to the mangosteen are a class of phytochemicals known as xanthones that have been reported to display significant anti-cancer and anti-tumor activities, specifically through the promotion of apoptosis, targeting of specific cancer-related proteins, or modulation of cell signaling pathways. α-Mangostin, the most abundant xanthone isolated from the mangosteen, has received substantial attention as it has proven to be a potent phytochemical, specifically as an anticancer agent, in numerous different cancer cell studies and cancer animal models. While the mechanisms for these anticancer effects have been reported in many studies, lesser xanthones, including gartanin, β-mangostin, γ-mangostin, garcinone C, and garcinone E, and mangosteen extracts from the pericarp, roots, rind, and stem show promise for their anticancer activity but their mechanisms of action are not as well developed and remain to be determined. Mangosteen products appear safe and have been well tolerated in human clinical trials where they show antioxidant activity, though their clinical anticancer activity has not yet been evaluated. This review summarizes the work that has been done to explore and explain the anticancer and antitumor activities of α-mangostin, lesser xanthones, and mangosteen extracts in vitro, in vivo, and in humans in various cancers.

Indexed as

Garcinia mangostanaAnimalsAnticarcinogenic AgentsAntineoplastic Agents, PhytogenicHumansNeoplasmsPhytotherapyTreatment OutcomeXanthonesAnticarcinogenic AgentsAntineoplastic Agents, PhytogenicXanthonesAnticancerChemopreventionGarcinia mangostanaGarcinone C (PubChem CID: 44159808)Garcinone E (10298511)Gartanin (PubChem CID: 5281633)MangosteenProstate cancerXanthonesα-Mangostin (PubChem CID: 5281650)β-Mangostin (PubChem CID: 5495925)γ-Mangostin (PubChem CID: 5464078)

Identifiers

PMID34896543
PMCPMC9597473
OpenAlexW4200307880

What OpenQuestion holds

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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.