Evidence map›Paper›PMID 31357442›Full record

ArticleInternational journal of molecular sciences2019

Additive Pharmacological Interaction between Cisplatin (CDDP) and Histone Deacetylase Inhibitors (HDIs) in MDA-MB-231 Triple Negative Breast Cancer (TNBC) Cells with Altered Notch1 Activity-An Isobolographic Analysis.

Anna Wawruszak, Jarogniew J Luszczki, Joanna Kalafut, Karolina Okla, Marta Halasa, Adolfo Rivero-Muller, Andrzej Stepulak

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Optogenetic control of NOTCH1 signaling.Cell communication and signaling : CCS · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. International journal of molecular sciences · 2020
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Valproic Acid Synergizes With Cisplatin and CetuximabFrontiers in cell and developmental biology · 2020
    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

7 authors at 1 institution in 2 countries.

Anna WawruszakDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Chodzki 1 Street, 20-093 Lublin, Poland. anna.wawruszak@umlub.pl.ORCID 0000-0003-2388-4577
Jarogniew J LuszczkiIsobolographic Analysis Laboratory, Institute of Rural Health, Jaczewskiego 2 Street, 20-090 Lublin, Poland.
Joanna KalafutDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Chodzki 1 Street, 20-093 Lublin, Poland.
Karolina OklaThe First Department of Gynecologic Oncology and Gynecology, Medical University of Lublin, Staszica 16 Street, 20-081 Lublin, Poland.ORCID 0000-0001-7834-7520
Marta HalasaDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Chodzki 1 Street, 20-093 Lublin, Poland.
Adolfo Rivero-MullerDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Chodzki 1 Street, 20-093 Lublin, Poland.ORCID 0000-0002-9794-802X
Andrzej StepulakDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Chodzki 1 Street, 20-093 Lublin, Poland.
Medical University of Lublin · PL

Funding

Medical University of Lublin DS440/2018-2019Polish National Science Centre DEC-2015/17/B/NZ1/01777Polish National Science Centre DEC-2017/25/B/NZ4/02364The Polish Ministry of Science and Higher Education MNmb 510/2016-2017
6 · The paper itself

Abstract

The aim of this study was to investigate the influence of the Notch1 activity level on the pharmacological interaction between cisplatin (CDDP) and two histone deacetylase inhibitors (HDIs)-valproic acid (VPA) and vorinostat (SAHA) in the triple negative breast cancer (TNBC) cells. Stable breast cancer (BC) cell lines with increased and decreased activity of Notch1 were generated using a transfection method. The type of interaction between CDDP and the HDIs was determined by isobolographic analysis of cell proliferation in MDA-MB-231 cells with differential levels of Notch1 activity in vitro. The combination of CDDP/SAHA and CDDP/VPA in the MDA-MB-231 triple negative breast cancer (TNBC) cells with increased activity of Notch1, as well as CDDP/VPA in the MDA-MB-231 cells with decreased activity of Notch1, yielded an additive interaction, whereas additivity with a tendency towards antagonism was observed for the combination of CDDP/SAHA in MDA-MB-231 cells with the decreased activity of Notch1. Our studies demonstrated that SAHA and VPA might be considered as potential therapeutic agents in combination therapy with CDDP against TNBC with altered Notch1 activity.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationCisplatinDisease Models, AnimalDose-Response Relationship, DrugDrug AntagonismDrug InteractionsDrug SynergismFemaleGene ExpressionHistone Deacetylase InhibitorsHumansMiceMolecular StructureAntineoplastic AgentsCisplatinHistone Deacetylase InhibitorsNOTCH1 protein, humanReceptor, Notch1cisplatin (CDDP)histone deacetylase inhibitors (HDIs)isobolographic analysisNotch1 receptortriple negative breast cancer (TNBC)valproic acid (VPA)vorinostat (SAHA)

Identifiers

PMID31357442
PMCPMC6696008
OpenAlexW2962904778

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.