Evidence map›Paper›PMID 32632612›Full record

ArticleMolecular and cellular biochemistry2020

Mechanism analysis of toxicity of sodium sulfite to human hepatocytes L02.

Xu Han, Feifei Zhu, Liang Chen, Hong Wu, Tao Wang, Keping Chen

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 21 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

6 authors at 1 institution in 1 country.

Xu HanInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People's Republic of China.
Feifei ZhuInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People's Republic of China.
Liang ChenInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People's Republic of China.
Hong WuInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People's Republic of China.
Tao WangInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People's Republic of China.
Keping ChenInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People's Republic of China. kpchen@ujs.edu.cn.ORCID http://orcid.org/0000-0001-5254-2299
Jiangsu University · CN

Funding

National Natural Science Foundation of China No.31702186National Natural Science Foundation of China No.31802140National Natural Science Foundation of China No.31861143051National Natural Science Foundation of China No.31872425
6 · The paper itself

Abstract

Food additives are widely used in various food products to preserve the taste, color, and other qualities. However, if they are used improperly or exceed the standard, they will cause damage to the human body. Sulfite is a commonly used food additive to prevent oxidation from deteriorating the nutrients in foods, it has been widely used as a bleaching agent in the food industry for a long time. In this study, human hepatocytes L02 cells were used as a model cell line to evaluate the toxicity of sodium sulfite. The cell morphology and cell proliferation were affected by sodium sulfite treatment, and apoptosis was detected. Transcriptome sequencing showed 97 differentially expressed genes (DEGs) between the experimental group (IC50) and the control group (MOCK), and 27 differentially expressed genes related to cell apoptosis, metabolism and inflammation were selected for validation by qPCR. Among them, 13 significantly upregulated genes and 14 significantly downregulated genes were identified by qPCR. The results showed that with increase of sodium sulfite concentration, the morphology of L02 changed, cell proliferation and activity were inhibited, and sodium sulfite caused apoptosis in a concentration- and time-dependent manner. The resulting toxic mechanism inhibits proliferation, damages the mitochondrial integrity, and promotes apoptosis.

Indexed as

RNA-SeqCell LineCell ProliferationDose-Response Relationship, DrugGene Expression RegulationHepatocytesHumansSulfitessodium sulfiteSulfitesApoptosisCell activitySodium sulfiteToxicity mechanismTranscriptomic analysis

Identifiers

PMID32632612
OpenAlexW3039639370

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.