Evidence map›Paper›PMID 39144564›Full record

ArticleACS pharmacology & translational science2024

Ivermectin Synergizes with Modulated Electro-hyperthermia and Improves Its Anticancer Effects in a Triple-Negative Breast Cancer Mouse Model.

Kenan Aloss, Pedro Henrique Leroy Viana, Syeda Mahak Zahra Bokhari, Nino Giunashvili, Csaba András Schvarcz, Dániel Bócsi, Zoltán Koós, Zoltán Benyó, Péter Hamar

Abstract read
In one paragraph

Article in ACS pharmacology & translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Kenan AlossInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.ORCID https://orcid.org/0000-0003-4806-7477
Pedro Henrique Leroy VianaInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.
Syeda Mahak Zahra BokhariInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.ORCID https://orcid.org/0000-0002-6812-374X
Nino GiunashviliInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.
Csaba András SchvarczInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.
Dániel BócsiInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.
Zoltán KoósInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.
Zoltán BenyóInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.
Péter HamarInstitute of Translational Medicine, Semmelweis University, Üllői út 26., Budapest 1085, Hungary.ORCID https://orcid.org/0000-0002-1095-3564

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is the most aggressive breast cancer subtype, with limited treatment options. Modulated electro-hyperthermia (mEHT) is a novel adjuvant cancer therapy that induces selective cancer damage. However, mEHT upregulates heat shock protein beta 1 (HSPB1), a cancer-promoting stress chaperone molecule. Thus, we investigated whether ivermectin (IVM), an anthelmintic drug, may synergize with mEHT and enhance its anticancer effects by inhibiting HSPB1 phosphorylation. Isogenic 4T1 TNBC cells were inoculated into BALB/c mice and treated with mEHT, IVM, or a combination of both. IVM synergistically improved the tumor growth inhibition achieved by mEHT. Moreover, IVM downregulated mEHT-induced HSPB1 phosphorylation. Thus, the strongest cancer tissue damage was observed in the mEHT + IVM-treated tumors, coupled with the strongest apoptosis induction and proliferation inhibition. In addition, there was no significant body weight loss in mice treated with mEHT and IVM, indicating that this combination was well-tolerated. In conclusion, mEHT combined with IVM is a new, effective, and safe option for the treatment of TNBC.

Identifiers

PMID39144564
PMCPMC11320741

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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.