Evidence map›Paper›PMID 41826905›Full record

ArticleBMC cancer2026

Mumio and bladder cancer: unlocking its potential in 3D cell culture.

Zuzanna Fekner, Julia Sieracka, Paweł Dąbrowski, Łukasz Kaźmierski, Marta Rasmus, Arkadiusz Jundziłł, Tomasz Drewa, Dariusz Grzanka, Marta Pokrywczyńska, Tomasz Kloskowski

Abstract read
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zuzanna FeknerDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Julia SierackaDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Paweł DąbrowskiDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Łukasz KaźmierskiDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Marta RasmusDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Arkadiusz JundziłłDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Tomasz DrewaDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Dariusz GrzankaDepartment of Clinical Pathomorphology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Marta PokrywczyńskaDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Tomasz KloskowskiDepartment of Regenerative Medicine, Chair of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland. tomasz.kloskowski@cm.umk.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBladder cancer remains one of the most prevalent causes of cancer-related mortality worldwide. Mumio, a naturally occurring substance with a long-standing history of use in traditional medicine, has demonstrated therapeutic potential, including anticancer properties. This study aimed to evaluate the effects of a pharmaceutical formulation of Mumio on the growth of normal (SV-HUC-1) and cancerous (T24, 5637) bladder cell lines in 3D culture.

methodsSpheroids were generated using ultra-low attachment 96-well plates. Three concentrations of Mumio (LC₁₀, LC₅₀, LC₉₀), previously determined in 2D culture, were applied. Cells were incubated for 24, 48, and 72 h. Cell viability and caspase activity in 3D culture were assessed via luminescence-based assays. Hematoxylin–eosin (HE) and Ki-67 staining were performed to evaluate spheroid morphology and proliferation. Gene expression analysis was conducted to investigate molecular mechanisms.

resultsMumio exhibited dose-dependent cytotoxicity in 3D culture, with T24 cells showing the highest sensitivity compared to the control and the second bladder cancer cell line (5637) after all incubation times. Concentrations effective in 2D culture were less potent in 3D conditions. Proliferation rates decreased with increasing Mumio concentration and prolonged exposure. Molecular analysis revealed G1 phase cell cycle arrest and reduced DNA synthesis.

conclusionsMumio has potential in supportive bladder cancer treatment; however, its effectiveness, as observed in 2D culture, exhibited diminished efficacy when applied to 3D cultures. Further investigations are necessary, including the use of organoids or animal models, to confirm these properties.

Indexed as

Antineoplastic AgentsCell Culture Techniques, Three DimensionalUrinary Bladder NeoplasmsApoptosisCell Culture TechniquesCell Line, TumorCell ProliferationCell SurvivalHumansSpheroids, CellularAntineoplastic Agents3D cell cultureBladder cancerCell cycle arrestCytotoxicityMumioSpheroids

Identifiers

PMID41826905
PMCPMC13101165

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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.