Evidence map›Paper›PMID 34369271›Full record

ArticleBioengineered2021

Inhibition of HMGB1/RAGE axis suppressed the lipopolysaccharide (LPS)-induced vicious transformation of cervical epithelial cells.

Lifang You, Hongyin Cui, Fen Zhao, Huier Sun, Huanxin Zhong, Guoli Zhou, Xuejun Chen

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Involvement of the pyroptosis-HMGB1 axis in systemic diseases.Frontiers in cell and developmental biology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Involvement of role of HMGB1-NLRP3 pathway in systemic disorders.Frontiers in cell and developmental biology · 2025
    Review
  7. Review
  8. Therapeutic Significance of NLRP3 Inflammasome in Cancer: Friend or Foe?International journal of molecular sciences · 2024
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Article
  16. Article
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

7 authors at 1 institution in 1 country.

Lifang YouDepartment of Gynecology, First People's Hospital of Yuhang District, Hangzhou, China.
Hongyin CuiDepartment of Gynecology, First People's Hospital of Yuhang District, Hangzhou, China.
Fen ZhaoDepartment of Gynecology, First People's Hospital of Yuhang District, Hangzhou, China.
Huier SunDepartment of Gynecology, First People's Hospital of Yuhang District, Hangzhou, China.
Huanxin ZhongDepartment of Gynecology, First People's Hospital of Yuhang District, Hangzhou, China.
Guoli ZhouLaboratory Department, First People's Hospital of Yuhang District, Hangzhou, China.
Xuejun ChenDepartment of Gynecology, First People's Hospital of Yuhang District, Hangzhou, China.
First People's Hospital of Yuhang District · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chronic inflammation operates as one of the critical causes of cervical cancer. Activation of HMGB1/RAGE axis could induce the inflammation and lead to multiple types of cancer. However, whether the HMGB1/RAGE axis could affect the development of cervical cancer by regulating the inflammation is unclear. Here, we stimulated normal cervical epithelial cells with lipopolysaccharide (LPS). Next, the expression of RAGE in these cells was suppressed by the RAGE inhibitor. CCK-8 and wound healing assays were performed to detect the proliferation and invasion. To determine how inflammatory factors (IL-1β, IL-6 and TNF-α) expressed in supernatant of these cells, ELISA was conducted. Western blotting was used for the detection of the expression of pyroptosis-related proteins (NLRP3 and caspase4). It was found that stimulation of LPS enhanced the proliferation and invasion of normal cervical epithelial cells. The expression of inflammatory factors (IL-1β, IL-6 and TNF-α) in these cells was promoted as well. Application of RAGE inhibitor abolished the efficacy of LPS on these cells. Furthermore, LPS promoted the expression of NLRP3 and caspase4 in these cells while RAGE inhibitor exerted suppressive effects on the expression of these proteins. In summary, LPS-induced inflammation of normal cervical epithelial cells resulted in the malignant transformation of these cells by activating HMGB1/RAGE axis.

Indexed as

Cell LineCell Transformation, NeoplasticCervix UteriCytokinesEpithelial CellsFemaleHMGB1 ProteinHumansInflammationLipopolysaccharidesReceptor for Advanced Glycation End ProductsUterine Cervical NeoplasmsAGER protein, humanCytokinesHMGB1 ProteinHMGB1 protein, humanLipopolysaccharidesReceptor for Advanced Glycation End ProductsHMGB1/RAGE axisInflammationmalignant transformationnormal cervical epithelial cells

Identifiers

PMID34369271
PMCPMC8806497
OpenAlexW3188688736

What OpenQuestion holds

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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 OpenQuestion graph.