Evidence map›Paper›PMID 26811478›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Transketolase counteracts oxidative stress to drive cancer development.

Iris Ming-Jing Xu, Robin Kit-Ho Lai, Shu-Hai Lin, Aki Pui-Wah Tse, David Kung-Chun Chiu, Hui-Yu Koh, Cheuk-Ting Law, Chun-Ming Wong, Zongwei Cai, Carmen Chak-Lui Wong and 1 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07450833 (Assessing the Safety, Tolerability and Pharmacokinetics of Benfo-Oxythiamine), which is not on this map. Cited by 148 papers.

0numbers the graph read from it
0cells of the map it votes in
148citing papers in PubMed
10.1field-weighted citation impact, top 1% 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.

NCT07450833 phase1completednot on this mapstarted 2022, after this paper: background citation

Assessing the Safety, Tolerability and Pharmacokinetics of Benfo-Oxythiamine (B-OT) in Healthy Volunteers - An Open Label, Phase I Study

TypeinterventionalSponsorBenfovir AGRan2022 to 2022Enrolled48ConditionsHealthy VolunteersArmsBenfo-oxythiamine
3 · Its place in the literature

Who cites it

148 citing papers in PubMed, 251 citations in OpenAlex.

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88 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 2 countries.

Iris Ming-Jing XuDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China;
Robin Kit-Ho LaiDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China;
Shu-Hai LinDepartment of Chemistry,Hong Kong Baptist University, Hong Kong, SAR, China; State Key Laboratory of Environmental and Biological Analysis, Hong Kong Baptist University, Hong Kong, SAR, China;
Aki Pui-Wah TseDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China;
David Kung-Chun ChiuDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China;
Hui-Yu KohDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China;
Cheuk-Ting LawDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China;
Chun-Ming WongDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China; State Key Laboratory for Liver Research, The University of Hong Kong, Hong Kong, SAR, China.
Zongwei CaiDepartment of Chemistry,Hong Kong Baptist University, Hong Kong, SAR, China; State Key Laboratory of Environmental and Biological Analysis, Hong Kong Baptist University, Hong Kong, SAR, China;
Carmen Chak-Lui WongDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China; State Key Laboratory for Liver Research, The University of Hong Kong, Hong Kong, SAR, China iolng@hku.hk carmencl@pathology.hku.hk.
Irene Oi-Lin NgDepartment of Pathology, The University of Hong Kong, Hong Kong, SAR, China; State Key Laboratory for Liver Research, The University of Hong Kong, Hong Kong, SAR, China iolng@hku.hk carmencl@pathology.hku.hk.
University of Hong Kong · HKChinese University of Hong Kong · CNHong Kong Baptist University · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cells experience an increase in oxidative stress. The pentose phosphate pathway (PPP) is a major biochemical pathway that generates antioxidant NADPH. Here, we show that transketolase (TKT), an enzyme in the PPP, is required for cancer growth because of its ability to affect the production of NAPDH to counteract oxidative stress. We show that TKT expression is tightly regulated by the Nuclear Factor, Erythroid 2-Like 2 (NRF2)/Kelch-Like ECH-Associated Protein 1 (KEAP1)/BTB and CNC Homolog 1 (BACH1) oxidative stress sensor pathway in cancers. Disturbing the redox homeostasis of cancer cells by genetic knockdown or pharmacologic inhibition of TKT sensitizes cancer cells to existing targeted therapy (Sorafenib). Our study strengthens the notion that antioxidants are beneficial to cancer growth and highlights the therapeutic benefits of targeting pathways that generate antioxidants.

Indexed as

Oxidative StressAnimalsBase SequenceCarcinoma, HepatocellularCell Cycle CheckpointsCell DeathCell Line, TumorCell ProliferationFemaleGene Knockdown TechniquesGlucoseGlutathioneGlycolysisHumansLiver NeoplasmsMaleGlucoseGlutathioneNiacinamidePeroxidesPhenylurea CompoundsReactive Oxygen SpeciesRNA, MessengerSorafenibtert-butyl peroxideTransketolaseHCCmetabolismPPPROSTKT

Identifiers

PMID26811478
PMCPMC4760787
OpenAlexW2267831227

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.