Evidence map›Paper›PMID 35680841›Full record

ArticleCell death discovery2022

Sorafenib inhibits LPS-induced inflammation by regulating Lyn-MAPK-NF-kB/AP-1 pathway and TLR4 expression.

Xiaolian Li, Mingkun Xu, Jiaojiao Shen, Yuqin Li, Shaoping Lin, Min Zhu, Qiongni Pang, Xiujuan Tan, Jing Tang

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  7. Combining sorafenib andIranian journal of basic medical sciences · 2026
    Article
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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

9 authors at 2 institutions in 1 country.

Xiaolian Li *Department of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China.
Mingkun Xu *Department of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China.
Jiaojiao ShenDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China.
Yuqin LiDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China.
Shaoping LinDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China.
Min ZhuDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China.
Qiongni PangDepartment of Anesthesiology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, 510080, Guangzhou City, Guangdong Province, China.
Xiujuan TanDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China. 307319679@qq.com.ORCID http://orcid.org/0000-0003-0608-9045
Jing TangDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, 524000, Zhanjiang City, Guangdong Province, China. tanglitangjing@126.com.ORCID http://orcid.org/0000-0003-1646-3504
Guangdong Medical College · CNGuangdong Academy of Medical Sciences · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81873951National Natural Science Foundation of China (National Science Foundation of China) 82072208
6 · The paper itself

Abstract

Sorafenib is an anti-tumor drug widely used in clinical treatment, which can inhibit tyrosine kinase receptor on cell surface and serine/threonine kinase in downstream Ras/MAPK cascade signaling pathway of cells. Tyrosine kinase phosphorylation plays an important role in inflammatory mechanism, such as TLR4 tyrosine phosphorylation, MAPK pathway protein activation, and activation of downstream NF-кB. However, the effects of sorafenib on LPS-induced inflammatory reaction and its specific mechanism have still remained unknown. We found that sorafenib inhibited the phosphorylation of tyrosine kinase Lyn induced by LPS, thereby reducing the phosphorylation level of p38 and JNK, inhibiting the activation of c-Jun and NF-κB, and then inhibiting the expression of inflammatory factors IL-6, IL-1β, and TNF-α. Furthermore, sorafenib also decreased the expression of TLR4 on the macrophage membrane to inhibit the expression of inflammatory factors latterly, which may be related to the inactivation of Lyn. These results provide a new perspective and direction for the clinical treatment of sepsis.

Identifiers

PMID35680841
PMCPMC9184561
OpenAlexW4281777442

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.