Evidence map›Paper›PMID 39932626›Full record

ArticleMedical oncology (Northwood, London, England)2025

Evaluation of the anticancer effects of hydroxycinnamic acid isomers on breast cancer stem cells.

Tülin Burhanoğlu, Zehra Seda Halbutoğulları, Gulseren Turhal, Asuman Demiroglu-Zergeroglu

Abstract read
In one paragraph

Article in Medical oncology (Northwood, London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Ferulic andRSC advances · 2026
    Article
  3. The Therapeutic Potential ofMolecules (Basel, Switzerland) · 2025
    Article
  4. 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

4 authors.

Tülin BurhanoğluDepartment of Chemistry, Faculty of Science, Gebze Technical University, Kocaeli, Turkey. tulinb2@gmail.com.
Zehra Seda HalbutoğullarıCenter for Stem Cell and Gene Therapies Research and Practice, Kocaeli University, Kocaeli, Turkey.
Gulseren TurhalDepartment of Molecular Biology and Genetics, Faculty of Science, Gebze Technical University, Kocaeli, Turkey.
Asuman Demiroglu-ZergerogluDepartment of Molecular Biology and Genetics, Faculty of Science, Gebze Technical University, Kocaeli, Turkey. ademiroglu@gtu.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research on breast cancer stem cells (BCSCs) is crucial for improving our understanding of their roles in tumor resistance, metastasis, and relapse. This study investigated the anti-cancer effects of two isomers of hydroxycinnamic acids (HCA): para-coumaric acid (PCA) and ortho-coumaric acid (OCA) on breast cancer stem cells (BCSCs). The isolated and characterized stem cells contained CD44 + /CD24 surface markers, exhibited high levels of aldehyde dehydrogenase activity, and were able to form mammospheres. The evaluation of HCAs on stem cell proliferation, cell cycle, and apoptosis was conducted by comparing them with MCF-7, the luminal breast cancer cell line. The viability and immunoblot analyses demonstrated that HCA applications resulted in a dose-dependent decrease in the number of viable cells and inhibited phosphorylation of Extracellular regulated kinases 1/2 (ERK1/2). These findings were supported by the detection of suppressed colony formation and delayed wound-healing in HCA-exposed cells. E-cadherin expression increased in OCA-treated cells. Additionally, the arrest of G1/S phase progression and the downregulation of Cyclin D1 expression exhibited that OCA and PCA-induced cytostatic effects in BSCS cells. After treatment, the increased Annexin-V/7-AAD staining, along with elevated expression of caspase-3/7 and a decreased Bcl-2/Bax ratio, indicated apoptosis mediated by the activation of Janus kinase (JNK) and p38 Mitogen-activated kinase (p38 MAPK). In conclusion, both OCA and PCA exhibit anti-carcinogenic potential on BCSCs; However, OCA has a stronger effect and is becoming a promising candidate for further research.

Indexed as

Antineoplastic AgentsBreast NeoplasmsCoumaric AcidsNeoplastic Stem CellsApoptosisCell CycleCell ProliferationCell SurvivalFemaleHumansMCF-7 CellsAntineoplastic AgentsCoumaric AcidsAnti-cancer effectApoptosisBreast cancer stem cellMetastasisOrtho-coumaric acidPara-coumaric acid

Identifiers

PMID39932626
PMCPMC11814044

What OpenQuestion holds

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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.