Evidence map›Paper›PMID 32474842›Full record

ArticleCancer chemotherapy and pharmacology2020

Antitumor effects of ivermectin at clinically feasible concentrations support its clinical development as a repositioned cancer drug.

Mandy Juarez, Alejandro Schcolnik-Cabrera, Guadalupe Dominguez-Gomez, Alma Chavez-Blanco, Jose Diaz-Chavez, Alfonso Duenas-Gonzalez

Abstract read
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In one paragraph

Article in Cancer chemotherapy and pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.5field-weighted citation impact, top 21% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

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  7. Antitumor potential of ivermectin against T-cell lymphoma-bearing hosts.Medical oncology (Northwood, London, England) · 2025
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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

6 authors at 1 institution in 1 country.

Mandy JuarezInstituto Nacional de Cancerologia, Mexico City, Mexico.
Alejandro Schcolnik-CabreraInstituto Nacional de Cancerologia, Mexico City, Mexico.
Guadalupe Dominguez-GomezInstituto Nacional de Cancerologia, Mexico City, Mexico.
Alma Chavez-BlancoInstituto Nacional de Cancerologia, Mexico City, Mexico.
Jose Diaz-ChavezInstituto Nacional de Cancerologia, Mexico City, Mexico.
Alfonso Duenas-GonzalezInstituto Nacional de Cancerologia, Mexico City, Mexico. alfonso_duenasg@yahoo.com.ORCID http://orcid.org/0000-0002-2956-645X
Instituto Nacional de Cancerología · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIvermectin is an antiparasitic drug that exhibits antitumor effects in preclinical studies, and as such is currently being repositioned for cancer treatment. However, divergences exist regarding its employed doses in preclinical works. Therefore, the aim of this study was to determine whether the antitumor effects of ivermectin are observable at clinically feasible drug concentrations.

methodsTwenty-eight malignant cell lines were treated with 5 μM ivermectin. Cell viability, clonogenicity, cell cycle, cell death and pharmacological interaction with common cytotoxic drugs were assessed, as well as the consequences of its use on stem cell-enriched populations. The antitumor in vivo effects of ivermectin were also evaluated.

resultsThe breast MDA-MB-231, MDA-MB-468, and MCF-7, and the ovarian SKOV-3, were the most sensitive cancer cell lines to ivermectin. Conversely, the prostate cancer cell line DU145 was the most resistant to its use. In the most sensitive cells, ivermectin induced cell cycle arrest at G

conclusionOur results on the antitumor effects of ivermectin support its clinical testing.

Indexed as

AnimalsAntineoplastic AgentsAntiparasitic AgentsApoptosisBreast NeoplasmsCell CycleCell MovementCell ProliferationDrug RepositioningFemaleHumansIvermectinMiceMice, Inbred BALB CMice, NudeTumor Cells, CulturedAntineoplastic AgentsAntiparasitic AgentsIvermectinCancerCancer stem cellsDrug repurposingIvermectin

Identifiers

PMID32474842
OpenAlexW3029074664

What OpenQuestion holds

Textmetadata
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.