Evidence map›Paper›PMID 33673611›Full record

ArticleMolecules (Basel, Switzerland)2021

Prodigiosin Sensitizes Sensitive and Resistant Urothelial Carcinoma Cells to Cisplatin Treatment.

Lena Berning, David Schlütermann, Annabelle Friedrich, Niklas Berleth, Yadong Sun, Wenxian Wu, María José Mendiburo, Jana Deitersen, Hannah U C Brass, Margaretha A Skowron and 4 more

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 25 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Lena BerningInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
David SchlütermannInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Annabelle FriedrichInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Niklas BerlethInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Yadong SunInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Wenxian WuInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.ORCID 0000-0003-4059-5945
María José MendiburoInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Jana DeitersenInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Hannah U C BrassInstitute of Bioorganic Chemistry, Faculty of Mathematics and Natural Sciences, Heinrich Heine University, Forschungszentrum Jülich, Stetternicher Forst, 52428 Jülich, Germany.
Margaretha A SkowronDepartment of Urology, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.ORCID 0000-0003-2152-384X
Michèle J HoffmannDepartment of Urology, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.ORCID 0000-0002-6044-1671
Günter NiegischDepartment of Urology, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.ORCID 0000-0001-6929-8691
Jörg PietruszkaInstitute of Bioorganic Chemistry, Faculty of Mathematics and Natural Sciences, Heinrich Heine University, Forschungszentrum Jülich, Stetternicher Forst, 52428 Jülich, Germany.ORCID 0000-0002-9819-889X
Björn StorkInstitute of Molecular Medicine I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.ORCID 0000-0002-4167-7806
Heinrich Heine University Düsseldorf · DEForschungszentrum Jülich · DE

Funding

Bundesministerium für Bildung und Forschung 031B0918A - project 'AutoBiotech'Deutsche Forschungsgemeinschaft GK 2158Deutsche Forschungsgemeinschaft STO 864/5-1Deutsche Forschungsgemeinschaft STO 864/6-1
6 · The paper itself

Abstract

Cisplatin-based treatment is the standard of care therapy for urothelial carcinomas. However, complex cisplatin resistance mechanisms limit the success of this approach. Both apoptosis and autophagy have been shown to contribute to this resistance. Prodigiosin, a secondary metabolite from various bacteria, exerts different biological activities including the modulation of these two cellular stress response pathways. We analyzed the effect of prodigiosin on protein levels of different autophagy- and apoptosis-related proteins in cisplatin-sensitive and -resistant urothelial carcinoma cells (UCCs). Furthermore, we investigated the effect on cell viability of prodigiosin alone or in combination with cisplatin. We made use of four different pairs of cisplatin-sensitive and -resistant UCCs. We found that prodigiosin blocked autophagy in UCCs and re-sensitized cisplatin-resistant cells to apoptotic cell death. Furthermore, we found that prodigiosin is a potent anticancer agent with nanomolar IC

Indexed as

Antineoplastic AgentsApoptosisAutophagyBiological ProductsCell Line, TumorCell ProliferationCisplatinDrug Resistance, NeoplasmDrug SynergismDrug Therapy, CombinationHumansProdigiosinUrinary Bladder NeoplasmsAntineoplastic AgentsBiological ProductsCisplatinProdigiosinapoptosisautophagychemoresistancecisplatinprodigiosinurothelial carcinoma

Identifiers

PMID33673611
PMCPMC7957586
OpenAlexW3134744159

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.