Evidence map›Paper›PMID 33918514›Full record

ArticleMolecules (Basel, Switzerland)2021

The Anticancer Action of a Novel 1,2,4-Triazine Sulfonamide Derivative in Colon Cancer Cells.

Agnieszka Gornowicz, Anna Szymanowska, Mariusz Mojzych, Robert Czarnomysy, Krzysztof Bielawski, Anna Bielawska

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

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  12. MnOMolecules (Basel, Switzerland) · 2022
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  13. Pyrazolo[4,3-Molecules (Basel, Switzerland) · 2022
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  14. Preparation of Novel Pyrazolo[4,3-International journal of molecular sciences · 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

6 authors at 2 institutions in 1 country.

Agnieszka GornowiczDepartment of Biotechnology, Medical University of Bialystok, 15-222 Bialystok, Poland.ORCID 0000-0002-0945-7870
Anna SzymanowskaDepartment of Biotechnology, Medical University of Bialystok, 15-222 Bialystok, Poland.ORCID 0000-0003-4783-3336
Mariusz MojzychDepartment of Chemistry, Siedlce University of Natural Sciences and Humanities, 08-110 Siedlce, Poland.ORCID 0000-0002-9884-6068
Robert CzarnomysyDepartment of Synthesis and Technology of Drugs, Medical University of Bialystok, 15-222 Bialystok, Poland.ORCID 0000-0002-7148-6111
Krzysztof BielawskiDepartment of Synthesis and Technology of Drugs, Medical University of Bialystok, 15-222 Bialystok, Poland.
Anna BielawskaDepartment of Biotechnology, Medical University of Bialystok, 15-222 Bialystok, Poland.
Medical University of Białystok · PLUniversity of Siedlce · PL

Funding

Uniwersytet Medyczny w Bialymstoku SUB/2/DN/21/001/2229
6 · The paper itself

Abstract

Cancer therapy is one of the most important challenges of modern medical and chemical sciences. Among the many methods of combating cancer, chemotherapy plays a special role. Imperfect modern chemotherapy justifies continuing the search for new, more effective, and safe drugs. Sulfonamides are the classic group of chemotherapeutic drugs with a broad spectrum of pharmacological activity. Recent literature reports show that sulfonamide derivatives have anti-tumor activity in vitro and in vivo. The aim of the study was to synthesize a novel 1,2,4-triazine sulfonamide derivative and check its anticancer potential in DLD-1 and HT-29 colon cancer cells. The biological studies included MTT assay, DNA biosynthesis, cell cycle analysis, Annexin V binding assay, ethidium bromide/acridine orange staining, and caspase-8, -9, and -3/7 activity. The concentrations of important molecules (sICAM-1, mTOR, Beclin-1, cathepsin B) involved in the pathogenesis and poor prognosis of colorectal cancer were also evaluated by ELISA. We demonstrated that the novel compound was able to induce apoptosis through intrinsic and extrinsic pathways and was capable of decreasing sICAM-1, mTOR, cathepsin B concentrations, whereas increased Beclin-1 concentration was detected in both colon cancer cell lines. The novel compound represents promising multi-targeted potential in colorectal cancer, but further in vivo examinations are needed to confirm the claim.

Indexed as

Antineoplastic AgentsApoptosisBeclin-1CaspasesCell CycleCell Line, TumorCell ShapeCell SurvivalColonic NeoplasmsHumansSulfonamidesTOR Serine-Threonine KinasesTriazines1,2,4-triazineAntineoplastic AgentsBeclin-1CaspasesSulfonamidesTOR Serine-Threonine KinasesTriazines5-fluorouracilanticancer agentsapoptosiscell signalingcolorectal cancerpyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine

Identifiers

PMID33918514
PMCPMC8038278
OpenAlexW3149826509

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.