Evidence map›Paper›PMID 41212877›Full record

ArticlePloS one2025

Identification and validation of the important role of tryptophan-related gene CYP1B1 in the development and progression of sepsis.

Li-Hong Chen, Wei-Ru Lin, Hui-Rong Hu, Zhi-Yuan Chen, Yan-Hui Wang

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Li-Hong ChenDepartment of Anesthesiology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Wei-Ru LinDepartment of Ultrasound, Quanzhou Maternity and Children's Hospital, Quanzhou, Fujian, China.
Hui-Rong HuDepartment of Anesthesiology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Zhi-Yuan ChenDepartment of Anesthesiology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Yan-Hui WangDepartment of Anesthesiology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.ORCID https://orcid.org/0009-0002-1437-1526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTryptophan metabolism is involved in the progression and immune response of multiple diseases. However, the function of tryptophan metabolism in the immune characteristics of sepsis still needs to be elucidated.

methodsWe collected the datasets from the GEO database to extract data of blood samples RNA of patients with or without sepsis in GSE28750, GSE65682, GSE69528, and GSE137342. A serials of bioinformatics analysis, including batch normalization, differential analysis, and single-cell sequencing analysis were finished through R software. Finally, the effects of the candidate differential gene on sepsis progression were evaluated using transcription-quantitative polymerase chain reaction (RT-qPCR), transwell assays, western blot, and immunofluorescence staining.

resultsOne tryptophan metabolism-related DEG for sepsis were obtained, namely CYP1B1. The transcriptional and translational level of CYP1B1 were obviously increased in the blood tissues. Notably, CYP1B1 exhibited great discriminative ability for the diagnosis of sepsis. Furthermore, single-cell sequencing analysis further indicated that CYP1B1 was primarily expressed in monocytes, and its' expression level was significantly upregulated in monocytes activated by sepsis/LPS. Knockdown of CYP1B1 dramatically decreased the proinflammatory cytokines expression, blocked the migration of monocytes, and inhibited the expression of tryptophan metabolism-related protein TDO2.

conclusionCYP1B1 is involved in tryptophan metabolism and its upregulation can promote the progression and development of sepsis through activating monocytes.

Indexed as

Cytochrome P-450 CYP1B1SepsisTryptophanDisease ProgressionHumansMaleMonocytesCYP1B1 protein, humanCytochrome P-450 CYP1B1Tryptophan

Identifiers

PMID41212877
PMCPMC12599946

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