Evidence map›Paper›PMID 26413751›Full record

ArticleOncotarget2015

Application of mitochondrial pyruvate carrier blocker UK5099 creates metabolic reprogram and greater stem-like properties in LnCap prostate cancer cells in vitro.

Yali Zhong, Xiaoran Li, Dandan Yu, Xiaoli Li, Yaqing Li, Yuan Long, Yuan Yuan, Zhenyu Ji, Mingzhi Zhang, Jian-Guo Wen and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

53 citing papers in PubMed, 77 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

12 authors at 5 institutions in 2 countries.

Yali ZhongDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Xiaoran LiDepartment of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, University of Oslo, Montebello, Oslo, Norway.
Dandan YuDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Xiaoli LiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Yaqing LiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Yuan LongDepartment of Surgery, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Yuan YuanDepartment of Pathology, Capital Medical University, Beijing, China.
Zhenyu JiDepartment of Oncology, Henan Academy of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan Province, China.
Mingzhi ZhangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Jian-Guo WenDepartment of Urology Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Jahn M NeslandDepartment of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, University of Oslo, Montebello, Oslo, Norway.
Zhenhe SuoDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
First Affiliated Hospital of Zhengzhou University · CNOslo University Hospital · NOUniversity of Oslo · NOCapital Medical University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aerobic glycolysis is one of the important hallmarks of cancer cells and eukaryotic cells. In this study, we have investigated the relationship between blocking mitochondrial pyruvate carrier (MPC) with UK5099 and the metabolic alteration as well as stemness phenotype of prostatic cancer cells. It was found that blocking pyruvate transportation into mitochondrial attenuated mitochondrial oxidative phosphorylation (OXPHOS) and increased glycolysis. The UK5099 treated cells showed significantly higher proportion of side population (SP) fraction and expressed higher levels of stemness markers Oct3/4 and Nanog. Chemosensitivity examinations revealed that the UK5099 treated cells became more resistant to chemotherapy compared to the non-treated cells. These results demonstrate probably an intimate connection between metabolic reprogram and stem-like phenotype of LnCap cells in vitro. We propose that MPC blocker (UK5099) application may be an ideal model for Warburg effect studies, since it attenuates mitochondrial OXPHOS and increases aerobic glycolysis, a phenomenon typically reflected in the Warburg effect. We conclude that impaired mitochondrial OXPHOS and upregulated glycolysis are related with stem-like phenotype shift in prostatic cancer cells.

Indexed as

AcrylatesAntineoplastic AgentsApoptosisBlotting, WesternCell CycleCell ProliferationDrug Resistance, NeoplasmFlow CytometryGlycolysisHumansMaleMembrane Potential, MitochondrialMembrane Transport ProteinsMitochondriaMitochondrial Membrane Transport ProteinsMonocarboxylic Acid Transporters2-cyano-3-(1-phenylindol-3-yl)acrylateAcrylatesAntineoplastic AgentsMembrane Transport ProteinsMitochondrial Membrane Transport ProteinsMonocarboxylic Acid TransportersMPC1 protein, humanReactive Oxygen Speciesglycolysismitochondrial dysfunctionMPC blockerstemness

Identifiers

PMID26413751
PMCPMC4741963
OpenAlexW2164178708

What OpenQuestion holds

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LicenceCC BY
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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.