Evidence map›Paper›PMID 39304650›Full record

ArticleCell death & disease2024

Mesenchymal stem cells in tumor microenvironment: drivers of bladder cancer progression through mitochondrial dynamics and energy production.

Enguang Yang, Suoshi Jing, Fang Wang, Hanzhang Wang, Shengjun Fu, Li Yang, Junqiang Tian, Dragan J Golijanin, Wafik S El-Deiry, Liang Cheng and 1 more

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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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

11 authors.

Enguang Yang *Institute of Urology, Lanzhou University Second Hospital; Key Laboratory of Gansu Province for Urological Diseases; Gansu Urological Clinical Center, Lanzhou, China.
Suoshi Jing *Institute of Urology, Lanzhou University Second Hospital; Key Laboratory of Gansu Province for Urological Diseases; Gansu Urological Clinical Center, Lanzhou, China.
Fang Wang *Medical experiment center, Lanzhou University, Lanzhou, China.
Hanzhang WangThe Legorreta Cancer Center at Brown University, Department of Pathology and Laboratory Medicine, The Warren Albert Medical School of Brown University, Brown University Health, Providence, RI, USA.
Shengjun FuInstitute of Urology, Lanzhou University Second Hospital; Key Laboratory of Gansu Province for Urological Diseases; Gansu Urological Clinical Center, Lanzhou, China.
Li YangInstitute of Urology, Lanzhou University Second Hospital; Key Laboratory of Gansu Province for Urological Diseases; Gansu Urological Clinical Center, Lanzhou, China.
Junqiang TianInstitute of Urology, Lanzhou University Second Hospital; Key Laboratory of Gansu Province for Urological Diseases; Gansu Urological Clinical Center, Lanzhou, China.
Dragan J GolijaninDivision of Urology, Department of Surgery, The Warren Albert Medical School of Brown University, The Miriam Hospital, Providence, RI, USA.
Wafik S El-DeiryThe Legorreta Cancer Center at Brown University, Department of Pathology and Laboratory Medicine, The Warren Albert Medical School of Brown University, Brown University Health, Providence, RI, USA.ORCID 0000-0002-9577-8266
Liang ChengThe Legorreta Cancer Center at Brown University, Department of Pathology and Laboratory Medicine, The Warren Albert Medical School of Brown University, Brown University Health, Providence, RI, USA. liang_cheng@brown.edu.ORCID 0000-0001-6049-5293
Zhiping WangInstitute of Urology, Lanzhou University Second Hospital; Key Laboratory of Gansu Province for Urological Diseases; Gansu Urological Clinical Center, Lanzhou, China. wangzplzu@163.com.ORCID 0000-0002-8140-591X

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82060459
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) in tumor microenvironment (TME) are crucial for the initiation, development, and metastasis of cancer. The impact and mechanism of MSCs on bladder cancer are uncertain. Here we analyzed 205 patient samples to explore the relationships between tumor-stroma ratio and clinicopathological features. A co-culture model and nude mouse transplantation were used to explore the biological roles and molecular mechanisms of MSCs on bladder cancer cells. We found that a high tumor-stroma ratio was significantly associated with a larger tumor size and higher T stage, pathological grade, number of vascular invasions, and poor overall survival. MSCs in TME promoted the ability of bladder cancer cells to proliferate, migrate, and invade in vitro and in vivo. Next, we demonstrated that MSCs enhance mitochondrial autophagy and mitochondrial biogenesis of bladder cancer cells, and increase energy production, thereby promoting bladder cancer cell progression. Kynurenine (Kyn) produced by MSCs could enhance mitochondrial function by activating the AMPK pathway. IDO1 inhibitor could reverse the tumor‑promoting effects of MSCs in vitro and in vivo. Our results demonstrated that tryptophan metabolites Kyn of MSCs in TME could enhance mitochondrial function by activating the AMPK pathway, thereby promoting bladder cancer cell progression.

Indexed as

Disease ProgressionMesenchymal Stem CellsMice, NudeMitochondrial DynamicsTumor MicroenvironmentUrinary Bladder NeoplasmsAgedAnimalsCell Line, TumorCell MovementCell ProliferationCoculture TechniquesEnergy MetabolismFemaleHumansIndoleamine-Pyrrole 2,3,-DioxygenaseIndoleamine-Pyrrole 2,3,-DioxygenaseKynurenine

Identifiers

PMID39304650
PMCPMC11415494

What OpenQuestion holds

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Registered trials

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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.