Evidence map›Paper›PMID 30766596›Full record

ArticleAfrican health sciences2018

Inhibition of cell proliferation, migration and colony formation of LS174T Cells by carbonic anhydrase inhibitor.

Fuat Karakuş, Ergül Eyol, Kadir Yılmaz, Songül Ünüvar

Open access · diamondAbstract read
In one paragraph

Article in African health sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  5. Evaluation of Antiproliferative Properties of CoMnZn-FePharmaceuticals (Basel, Switzerland) · 2024
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  12. Nobiletin Inhibits Cell ViabilityFrontiers in pharmacology · 2019
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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

4 authors at 2 institutions in 1 country.

Fuat KarakuşDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, İnönü University, Malatya, Turkey.
Ergül EyolDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, İnönü University, Malatya, Turkey.
Kadir YılmazDepartment of Chemistry, Faculty of Art and Science, İnönü University, Malatya, Turkey.
Songül ÜnüvarDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, İnönü University, Malatya, Turkey.
Inonu University · TREge University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastasis is the leading cause of cancer deaths. Migration of tumor cells is an important stage in metastasis. Therefore, recent studies have focused on clarifying migration and migration-dependent cell functions such as angiogenesis, wound healing, and invasion.

objectivesIn the present study, we aimed to investigate the effect of acetazolamide, which is a classical carbonic anhydrase inhibitor, on the cell viability, migration, and colony forming capacity of human LS174T colorectal cancer cells.

methodsThree different cell culture techniques (MTT test, wound healing and clonogenic assay) were performed in this in vitro study on colorectal cancer cells.

resultsAcetazolamide reduced the cell viability, migration and colony formation ability of cells depending on dose. There was no significant difference between the cells treated with acetazolamide with 1 µM dose and the control. However, it can be concluded that acetazolamide exerts its effect on human colorectal cancer cells at 10-1000 µM concentrations.

conclusionAcetazolamide was observed to significantly inhibit the cell viability, colony forming capacity, and migration ability in the culture medium of LS174T cells. This inhibitor effect of acetazolamide was observed to be dependent on the concentration in medium.

Indexed as

AcetazolamideCarbonic Anhydrase InhibitorsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDose-Response Relationship, DrugHumansAcetazolamideCarbonic Anhydrase Inhibitorscarbonic anhydrase inhibitorcolorectal carcinomaLS174T

Identifiers

PMID30766596
PMCPMC6354875
OpenAlexW2903405098

What OpenQuestion holds

Textmetadata
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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.