Evidence map›Paper›PMID 41084228›Full record

ArticleCell adhesion & migration2025

Telomerase inhibitors - TMPyP4, BIBR 1532 and imetelstat - alter the adhesion potential of breast cancer MCF7 and MDA-MB-231 cells that leads to impaired ability to form spheroids.

Przemysław Kopczyński, Aleksandra Romaniuk-Drapała, Kinga Rygiel, Jacek Kujawski, Błażej Rubiś

Abstract read
In one paragraph

Article in Cell adhesion & migration, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Przemysław KopczyńskiCentre for Orthodontic Mini-Implants, Department and Clinic of Maxillofacial Orthopedics and Orthodontics, Poznan University of Medical Sciences Poznan, Poland.ORCID 0000-0001-7216-9479
Aleksandra Romaniuk-DrapałaDepartment of Clinical Chemistry and Molecular Diagnostics, Poznan University of Medical Sciences Poznan, Poland.ORCID 0000-0002-3922-8729
Kinga RygielDepartment of Clinical Chemistry and Molecular Diagnostics, Poznan University of Medical Sciences Poznan, Poland.
Jacek KujawskiChair and Department of Organic Chemistry, Faculty of Pharmacy, Poznan University of Medical Sciences Poznań, Poland.ORCID 0000-0001-6279-4887
Błażej RubiśDepartment of Clinical Chemistry and Molecular Diagnostics, Poznan University of Medical Sciences Poznan, Poland.ORCID 0000-0003-1730-0176

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We assessed the influence of telomerase inhibitors TMPyP4, BIBR 1532, or imetelstat on the ability of MCF7 and MDA-MB-231 breast cancer cells to form spheroids. TMPyP4 significantly impaired the adhesion potential and ability of both cell lines to form spheroids. BIBR 1532 treatment did not show any effect in MCF7 while it showed some effect in MDA-MB-231 cells, although this effect was less extensive comparing to TMPyP4. Application of Imetelstat provoked a dispersion effect in both cell lines but more single, separated distant cells were observed. Molecular docking and molecular dynamic studies showed that both BIBR 1532 and TMPyP4 exhibited affinity toward the structure of a G-quadruplex of human telomeric RNA (TERRA2 G4s) and the catalytic subunit of telomerase, hTERT. We showed that the use of telomerase expression/activity inhibitors to reduce the adhesive capacity and metastatic potential of breast cancer cells may play a significant role in anticancer strategy.

Indexed as

AminobenzoatesBreast NeoplasmsEnzyme InhibitorsPyridinesSpheroids, CellularTelomeraseCell AdhesionCell Line, TumorFemaleG-QuadruplexesHumansMCF-7 CellsMDA-MB-231 CellsMolecular Docking SimulationNaphthalenesOligonucleotidesAminobenzoatesBIBR 1532Enzyme InhibitorsimetelstatNaphthalenesOligonucleotidesPorphyrinsPyridinesTelomerasetetra(4-N-methylpyridyl)porphineBIBR 1532breast cancerhTERTimetelstattelomeraseTMPyP4

Identifiers

PMID41084228
PMCPMC12530491

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Registered trials

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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.