Evidence map›Paper›PMID 42764637›Full record

ArticleChemistry & biodiversity2026

Evaluating the Anticancer and Anti-Angiogenic Efficacy of Bergaptol in 2D and 3D Tumor Microtissue Models.

Buse Bekar, Handan Sevim Akan

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Buse BekarFaculty of Science, Department of Biology, Hacettepe University, Beytepe, Ankara, Turkey.ORCID https://orcid.org/0009-0001-1308-4915
Handan Sevim AkanFaculty of Science, Department of Biology, Hacettepe University, Beytepe, Ankara, Turkey.ORCID https://orcid.org/0000-0002-8511-5258

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Furanocoumarins are plant-derived compounds with diverse biological activities and emerging therapeutic potential. This study evaluated the anticancer and anti-angiogenic properties of bergaptol by using MDA-MB-231, HepG2, and HeLa cancer cell lines, as well as HUVEC endothelial cells, with HDFs serving as the healthy control group. Cell viability, apoptosis, cell-cycle progression, and angiogenesis were evaluated using complementary two-dimensional (2D) and three-dimensional (3D) experimental models. Bergaptol exhibited selective cytotoxicity toward cancer and endothelial cells, with no apparent cytotoxicity toward HDFs. Treatment induced apoptosis, disrupted cell-cycle progression, and suppressed angiogenic activity. In 3D models, bergaptol reduced spheroid viability, diminished spheroid size, and decreased endothelial cell content. An ex vivo assay, the chorioallantoic membrane (CAM) assay, corroborated these observations, demonstrated a substantial inhibition of neovascularization, and further supports its anti-angiogenic potential. These findings demonstrate that bergaptol exhibits both anticancer and anti-angiogenic activity in 2D and 3D experimental models supporting further evaluation of bergaptol as a potential anticancer agent.

Indexed as

Angiogenesis InhibitorsAntineoplastic AgentsFurocoumarinsAnimalsApoptosisCell CycleCell Line, TumorCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansHuman Umbilical Vein Endothelial CellsStructure-Activity RelationshipAngiogenesis InhibitorsAntineoplastic AgentsFurocoumarinsangiogenesisanti‐cancer moleculesbergaptolfuranocoumarinsmicrotissues

Identifiers

PMID42764637
PMCPMC13591067

What Socratic holds

Textmetadata
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 Socratic graph.