Evidence map›Paper›PMID 41104342›Full record

ArticleFrontiers in pharmacology2025

Unraveling the influence of α-mangostin on MDA-MB-231 cell line via WNT/β-catenin signaling pathway:

Riezki Amalia, Citra Dewi, Adryan Fristiohady, Taufik Muhammad Fakih, Muchtaridi Muchtaridi

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. 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

5 authors.

Riezki AmaliaDepartment of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran, Bandung, Indonesia.
Citra DewiLaboratory of Translational Pharmaceutical Research, Faculty of Pharmacy, Universitas Padjadjaran, Bandung, Indonesia.
Adryan FristiohadyPharmacy Study Program, Faculty of Pharmacy, Universitas Halu Oleo, Kendari, Indonesia.
Taufik Muhammad FakihDepartment of Pharmaceutical Analysis and Medical Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Bandung, Indonesia.
Muchtaridi MuchtaridiDepartment of Pharmaceutical Analysis and Medical Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Bandung, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Wnt/β-catenin signaling pathway is critically involved in breast cancer progression, particularly in the triple-negative subtype (TNBC). Aberrant activation of this pathway promotes tumor proliferation, with β-catenin functioning as a central effector regulated by GSK-3β-mediated phosphorylation and degradation. Despite its therapeutic significance, no selective Wnt/β-catenin inhibitors have been clinically approved, underscoring the need for alternative strategies. Natural compounds such as α-mangostin have emerged as potential modulators of this pathway. This study investigates the potential of α-mangostin, a natural xanthone compound, to suppress Wnt/β-catenin signaling through complementary

Indexed as

CCND1GSK-3βMYCtriple negative breast cancerWnt/β-cateninα-mangostin

Identifiers

PMID41104342
PMCPMC12521263

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.