Evidence map›Paper›PMID 39935420›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2025

Selisistat, a SIRT1 inhibitor, enhances paclitaxel activity in luminal and triple-negative breast cancer: in silico, in vitro, and in vivo studies.

Anna Wawruszak, Jarogniew Luszczki, Damian Bartuzi, Joanna Kalafut, Estera Okon, Arkadiusz Czerwonka, Andrzej Stepulak

Abstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Sirtuins in Women's Health.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  8. Article
  9. Review
  10. Review
  11. Design, synthesis, characterization,Future medicinal chemistry · 2025
    Article
  12. 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

7 authors.

Anna WawruszakDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Jarogniew LuszczkiDepartment of Occupational Medicine, Medical University of Lublin, Lublin, Poland.
Damian BartuziDepartment of Synthesis and Chemical Technology of Pharmaceutical Substances with Computer Modelling Laboratory, Medical University of Lublin, Lublin, Poland.
Joanna KalafutDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Estera OkonDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Arkadiusz CzerwonkaDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Andrzej StepulakDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sirtuins (SIRTs) are NAD+-dependent histone deacetylases, which play a key role in cancer progression; however, their prognostic values in breast cancer (BC) remain a subject of debate and controversy. Accumulative evidence suggests that each sirtuin possesses individual character, implicating its role in the regulation of multifaceted biological functions leading to BC initiation, progression and metastasis. Selisistat (EX527) is a potent, cell permeable, highly selective SIRT1 inhibitor. In the study, the tumour-suppressive effects of the SIRT1 inhibitor EX527 (selisistat) alone and in combination with paclitaxel (PAX) in different breast cancer cell lines and zebrafish xenograft models were investigated. The type of pharmacological drug-drug interaction between EX527 and PAX was determined using the isobolographic method. EX527 and PAX used individually inhibited proliferation, induced apoptosis and caused cell cycle arrest in G1 and subG1/G2 phases. Interestingly, the combination of these compounds used in the 1:1 dose-ratio augmented all these effects (IC

Indexed as

Antineoplastic AgentsAntineoplastic Agents, PhytogenicCarbazolesHistone Deacetylase InhibitorsPaclitaxelSirtuin 1Triple Negative Breast NeoplasmsAnimalsApoptosisCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleHumansMolecular Structure6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamideAntineoplastic AgentsAntineoplastic Agents, PhytogenicCarbazolesHistone Deacetylase InhibitorsPaclitaxelSIRT1 protein, humanSirtuin 1Breast cancerhistone deacetylase inhibitorpaclitaxelselisistatsirtuin inhibitor

Identifiers

PMID39935420
PMCPMC11823383

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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.