Evidence map›Paper›PMID 31661890›Full record

ArticleCells2019

Dimethylfumarate Inhibits Colorectal Carcinoma Cell Proliferation: Evidence for Cell Cycle Arrest, Apoptosis and Autophagy.

Irina Kaluzki, Tsige Hailemariam-Jahn, Monika Doll, Roland Kaufmann, Panagiotis Balermpas, Nadja Zöller, Stefan Kippenberger, Markus Meissner

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

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  15. Tight association of autophagy and cell cycle in leukemia cells.Cellular & molecular biology letters · 2022
    Article
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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

8 authors at 1 institution in 1 country.

Irina KaluzkiDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. irina.kaluzki@kgu.de.
Tsige Hailemariam-JahnDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. rita_th@web.de.
Monika DollDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. monika.doll@kgu.de.
Roland KaufmannDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. roland.kaufmann@kgu.de.
Panagiotis BalermpasDepartment of Radiation Oncology, Universitäts Spital, 8091 Zürich, Switzerland. panagiotis.balermpas@usz.ch.
Nadja ZöllerDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. nadja.zoeller@kgu.de.
Stefan KippenbergerDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. kippenberger@em.uni-frankfurt.de.
Markus MeissnerDepartment of Dermatology, Venereology and Allergology, Goethe-University, 60323 Frankfurt am Main, Germany. markus.meissner@kgu.de.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have proven that Dimethylfumarate (DMF) has a marked anti-proliferative impact on diverse cancer entities e.g., on malignant melanoma. To explore its anti-tumorigenic potential, we examined the effects of DMF on human colon carcinoma cell lines and the underlying mechanisms of action. Human colon cancer cell line HT-29 and human colorectal carcinoma cell line T84 were treated with or without DMF. Effects of DMF on proliferation, cell cycle progression, and apoptosis were analyzed mainly by Bromodeoxyuridine (BrdU)- and Lactatdehydrogenase (LDH)assays, caspase activation, flowcytometry, immunofluorescence, and immunoblotting. In addition, combinational treatments with radiation and chemotherapy were performed. DMF inhibits cell proliferation in both cell lines. It was shown that DMF induces a cell cycle arrest in G0/G1 phase, which is accompanied by upregulation of p21 and downregulation of cyclin D1 and Cyclin dependent kinase (CDK)4. Furthermore, upregulation of autophagy associated proteins suggests that autophagy is involved. In addition, the activation of apoptotic markers provides evidence that apoptosis is involved. Our results show that DMF supports the action of oxaliplatin in a synergetic manner and failed synergy with radiation. We demonstrated that DMF has distinct antitumorigenic, cell dependent effects on colon cancer cells by arresting cell cycle in G0/G1 phase as well as activating both the autophagic and apoptotic pathways and synergizes with chemotherapy.

Indexed as

ApoptosisAutophagyCell CycleCell Cycle CheckpointsCell Line, TumorCell ProliferationColorectal NeoplasmsCutaneous Malignant MelanomaCyclin-Dependent Kinase Inhibitor p21Dimethyl FumarateHumansMelanomaSkin NeoplasmsCyclin-Dependent Kinase Inhibitor p21Dimethyl Fumarateautophagycaspase-8cell cycle arrestcolorectal carcinomacyclin D1dimethylfumarateLC3 I/IIp21p62

Identifiers

PMID31661890
PMCPMC6912700
OpenAlexW2981426281

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.