Evidence map›Paper›PMID 35698168›Full record

ArticleBMC pharmacology & toxicology2022

Exploring the potential of taurolidine in inducing mobilization and detachment of colon cancer cells: a preliminary in-vitro study.

Agata Mikolajczyk, Veria Khosrawipour, Hien Lau, Shiri Li, Pawel Migdal, Maya Karine Labbé, Wojciech Kielan, Jakub Nicpon, Sven Stieglitz, Tanja Khosrawipour

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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  8. Frontiers in oncology · 2022
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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

10 authors at 6 institutions in 3 countries.

Agata Mikolajczyk *Department of Biochemistry and Molecular Biology, Wroclaw University of Environmental and Life Sciences, 50-375, Wroclaw, Wroclaw, Poland.
Veria Khosrawipour *2nd Department of General Surgery and Surgical Oncology, Wroclaw Medical University, 50-556, Wroclaw, Wroclaw, Poland.
Hien LauDepartment of Surgery, University of California Irvine (UCI), Orange, CA, 92868, USA.
Shiri LiDepartment of Surgery, Weill Cornell Medical College New York Presbyterian Hospital, New York, 10065, USA.
Pawel MigdalDepartment of Environment, Hygiene and Animal Welfare, Wroclaw University of Environmental and Life Sciences, 50-375, Wroclaw, Wroclaw, Poland.
Maya Karine LabbéSchool of Dentistry, Wroclaw Medical University, 50-367, Wroclaw, Poland.
Wojciech Kielan2nd Department of General Surgery and Surgical Oncology, Wroclaw Medical University, 50-556, Wroclaw, Wroclaw, Poland.
Jakub NicponDepartment of Surgery, Faculty of Veterinary Sciences, Wroclaw University of Environmental and Life Sciences, 50-375, Wroclaw, Wroclaw, Poland.
Sven StieglitzDepartment Pulmonary Medicine, Petrus-Hospital Wuppertal, University of Witten-Herdecke, 42283, Wuppertal, Wuppertal, Germany.
Tanja KhosrawipourDepartment of Surgery (A), University-Hospital Düsseldorf, Moorenstrasse 5, 40225, Düsseldorf, Düsseldorf, Germany. tanja.khosrawipour@rub.de.ORCID 0000-0003-0233-551X
Wrocław University of Environmental and Life Sciences · PLUniversity of California, Irvine · USWroclaw Medical University · PLDüsseldorf University Hospital · DENewYork–Presbyterian Hospital · USUniversity of Wuppertal · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently, taurolidine has been intensively studied on a variety of in-vitro cancer cell-lines and first data exhibit encouraging antitumoral effects. While the clinical use of taurolidine is considered, some studies with in-vivo experiments contradict this beneficial effect and even indicate advanced cancer growth. The aim of this study is to further investigate this paradox in-vivo effect by taurolidine and closely analyze the interaction of cancer cells with the surrounding environment following taurolidine exposure.

methodsHT-29 (ATCC® HTB-38™) cells were treated with taurolidine at different concentrations and oxaliplatin using an in-vitro model. Morphological changes with respect to increasing taurolidine dosage were visualized and monitored using electron microscopy. Cytotoxicity of the agents as well as extent of cellular detachment by mechanical stress was measured for each substance using a colorimetric MTS assay.

resultsBoth taurolidine and oxaliplatin exhibit cell toxicity on colon cancer cells. Taurolidine reshapes colon cancer cells from round into spheric cells and further induces cluster formation. When exposed to mechanical stress, taurolidine significantly enhances detachment of adherent colon carcinoma cells compared to the control (p < 0.05) and the oxaliplatin group (p < 0.05). This effect is dose dependent.

conclusionsBeside its cytotoxic effects, taurolidine could also change mechanical interactions of cancer cells with their environment. Local cancer cell conglomerates could be mechanically mobilized and may cause metastatic growth further downstream. The significance of changes in cellular morphology caused by taurolidine as well as its interaction with the microenvironment must be further addressed in clinical cancer therapies. Further clinical studies are needed to evaluate both the safety and efficacy of taurolidine for the treatment of peritoneal surface malignancies.

Indexed as

Antineoplastic AgentsColonic NeoplasmsThiadiazinesHumansOxaliplatinTaurineTumor MicroenvironmentAntineoplastic AgentsOxaliplatinTaurinetaurolidineThiadiazinesCancerChemotherapyCytoreductive surgeryCytotoxicityMetastasisTaurolidine

Identifiers

PMID35698168
PMCPMC9195453
OpenAlexW4282552753

What OpenQuestion holds

Textmetadata
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.