Evidence map›Paper›PMID 31898444›Full record

ArticleJournal of Zhejiang University. Science. B

Toxicity and metabolism of 3-bromopyruvate in Caenorhabditis elegans.

Qiao-Ling Gu, Yan Zhang, Xi-Mei Fu, Zhao-Lian Lu, Yao Yu, Gen Chen, Rong Ma, Wei Kou, Yong-Mei Lan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Zhejiang University. Science. B. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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  4. Cytochromes P450 ofBiomolecules · 2022
    Review
  5. Xenobiotic metabolism and transport inJournal of toxicology and environmental health. Part B, Critical reviews · 2021
    Review
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

9 authors at 4 institutions in 1 country.

Qiao-Ling GuThe Institute of Minority Physique and Health, Medical College of Northwest University for Nationalities, Lanzhou 730030, China.
Yan ZhangDepartment of Anesthesiology, First Hospital, Lanzhou University, Lanzhou 730000, China.
Xi-Mei FuPathogen Biology Institute, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China.
Zhao-Lian LuPathogen Biology Institute, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China.
Yao YuPathogen Biology Institute, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China.
Gen ChenDepartment of Microbiology, School of Basic Medical Sciences, Guilin Medical University, Guilin 541100, China.
Rong MaThe Institute of Minority Physique and Health, Medical College of Northwest University for Nationalities, Lanzhou 730030, China.
Wei KouThe Institute of Minority Physique and Health, Medical College of Northwest University for Nationalities, Lanzhou 730030, China.
Yong-Mei LanThe Institute of Minority Physique and Health, Medical College of Northwest University for Nationalities, Lanzhou 730030, China.
Northwest Minzu University · CNLanzhou University · CNFirst Hospital of Lanzhou University · CNGuilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we aimed to evaluate the toxic effects, changes in life span, and expression of various metabolism-related genes in Caenorhabditis elegans, using RNA interference (RNAi) and mutant strains, after 3-bromopyruvate (3-BrPA) treatment. C. elegans was treated with various concentrations of 3-BrPA on nematode growth medium (NGM) plates, and their survival was monitored every 24 h. The expression of genes related to metabolism was measured by the real-time fluorescent quantitative polymerase chain reaction (qPCR). Nematode survival in the presence of 3-BrPA was also studied after silencing three hexokinase (HK) genes. The average life span of C. elegans cultured on NGM with 3-BrPA was shortened to 5.7 d compared with 7.7 d in the control group. hxk-1, hxk-2, and hxk-3 were overexpressed after the treatment with 3-BrPA. After successfully interfering hxk-1, hxk-2, and hxk-3, the 50% lethal concentration (LC

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCytochrome P-450 Enzyme SystemHexokinasePyruvatesRNA, MessengerbromopyruvateCaenorhabditis elegans ProteinsCYP35 protein, C elegansCytochrome P-450 Enzyme SystemHexokinasePyruvatesRNA, Messenger3-Bromopyruvate; Caenorhabditis elegans; Hexokinase; Cytochrome P450

Identifiers

PMID31898444
PMCPMC6964992
OpenAlexW3000598629

What OpenQuestion holds

Textmetadata
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.