Evidence map›Paper›PMID 33562019›Full record

ArticleInternational journal of molecular sciences2021

Caffeic Acid Enhances the Anti-Leukemic Effect of Imatinib on Chronic Myeloid Leukemia Cells and Triggers Apoptosis in Cells Sensitive and Resistant to Imatinib.

Giordana Feriotto, Federico Tagliati, Riccardo Giriolo, Fabio Casciano, Claudio Tabolacci, Simone Beninati, Mahmud Tareq Hassan Khan, Carlo Mischiati

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Design, Spectral Insights, and Enhanced Antioxidant Potential of Novel Phenothiazine DerivativesAnti-inflammatory & anti-allergy agents in medicinal chemistry · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Adjuvant Properties of Caffeic Acid in Cancer Treatment.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Pro-Apoptotic Potential ofPharmaceutics · 2021
    Article
  19. Flavonoids: A Myth or a Reality for Cancer Therapy?Molecules (Basel, Switzerland) · 2021
    Review
  20. The Anti-Leukemic Activity of Natural Compounds.Molecules (Basel, Switzerland) · 2021
    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

8 authors at 4 institutions in 2 countries.

Giordana FeriottoDepartment of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.
Federico TagliatiDepartment of Neuroscience and Rehabilitation, University of Ferrara, 44121 Ferrara, Italy.
Riccardo GirioloDepartment of Neuroscience and Rehabilitation, University of Ferrara, 44121 Ferrara, Italy.
Fabio CascianoDepartment of Translational Medicine and LTTA Centre, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0002-6431-3335
Claudio TabolacciDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0001-5001-285X
Simone BeninatiDepartment of Biology, University of Rome "Tor Vergata", 00133 Rome, Italy.
Mahmud Tareq Hassan KhanDrug Discovery & Design, AuraDynamics AS, 9012 Tromsø, Norway.ORCID 0000-0002-0748-5747
Carlo MischiatiDepartment of Neuroscience and Rehabilitation, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0002-0029-2205
University of Ferrara · ITBayer (Norway) · NOIstituto Superiore di Sanità · ITUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the phenolic acids tested on the K562 cell line, a model of chronic myeloid leukemia (CML), caffeic acid (CA) was biologically active on sensitive and imatinib (IM)-resistant cells at micro-molar concentration, either in terms of reduction of cell proliferation or triggering of apoptosis. The CA treatment provoked mitochondrial membrane depolarization, genomic DNA fragmentation and phosphatidylserine exposure, hallmarks of apoptosis. Cell cycle analysis following the treatment with comparable cytotoxic concentrations of IM or CA showed marked differences in the distribution profiles. The reduction of cell proliferation by CA administration was associated with increased expression of two cell cycle repressor genes,

Indexed as

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCaffeic AcidsCell Cycle ProteinsCell Line, TumorCell ProliferationCyclin-Dependent Kinase Inhibitor p21DNA FragmentationDrug Resistance, NeoplasmDrug SynergismForkhead Transcription FactorsHumansImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMitochondrial MembranesAntineoplastic AgentsCaffeic AcidsCDKN1A protein, humanCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p21Forkhead Transcription FactorsFOXN3 protein, humanImatinib Mesylateapoptosiscaffeic acidchronic myeloid leukemiaimatinibresistance

Identifiers

PMID33562019
PMCPMC7914550
OpenAlexW3129113216

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.