Evidence map›Paper›PMID 39134813›Full record

ArticleBulletin of experimental biology and medicine2024

Anticancer Effects of Spiperone in C57BL/6 Mice with Emphysema and Lung Carcinoma.

N N Ermakova, M A Zhukova, E S Pan, V Yu Pan, S G Morozov, A A Kubatiev, A M Dygai, E G Skurikhin

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Article in Bulletin of experimental biology and medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

N N ErmakovaResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.
M A ZhukovaResearch Institute of General Pathology and Pathophysiology, Moscow, Russia. mashazyk@gmail.com.
E S PanResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.
V Yu PanResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.
S G MorozovResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.
A A KubatievResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.
A M DygaiResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.
E G SkurikhinResearch Institute of General Pathology and Pathophysiology, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The antitumor and antimetastatic activity of dopamine D2 receptor antagonists spiperone was studied in C57BL/6 mice in a model of combined pathology (emphysema and lung cancer). Emphysema was induced by administration of LPS and cigarette smoke extract. Lung cancer was induced by injection of Lewis lung carcinoma cells into the lung. It has been shown that under conditions of combined lung pathology, spiperone prevents inflammatory infiltration and emphysematous expansion of the lungs and reduces the size of the primary tumor node, the number of metastases, and the area of the lungs affected by metastases. Spiperone reduces the number of cancer stem cells (CSCs) in the lungs and blood of mice with combined pathology. CSCs isolated from the lungs and blood of mice with combined pathology treated with spiperone had a significantly lower potential to form a tumorosphere in vitro than CSCs from untreated mice with emphysema and lung carcinoma. Thus, blockade of dopamine D2 receptors is a promising approach for correcting combined lung pathology and can be used in the development of a method for treating lung cancer in patients with emphysema.

Indexed as

Carcinoma, Lewis LungLung NeoplasmsMice, Inbred C57BLNeoplastic Stem CellsPulmonary EmphysemaSpiperoneAnimalsAntineoplastic AgentsDopamine D2 Receptor AntagonistsLipopolysaccharidesLungMaleMiceReceptors, Dopamine D2Antineoplastic AgentsDopamine D2 Receptor AntagonistsLipopolysaccharidesReceptors, Dopamine D2Spiperonecancer stem cellsLewis lung carcinomalung emphysemametastasesspiperone

Identifiers

PMID39134813

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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.