Evidence map›Paper›PMID 38725632›Full record

ReviewFrontiers in oncology2024

Multiple functions of HMGB1 in cancer.

Guangyao Lv, Menglin Yang, Keke Gai, Qiong Jia, Zhenzhen Wang, Bin Wang, Xueying Li

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

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  11. HMGB1: A Central Node in Cancer Therapy Resistance.International journal of molecular sciences · 2025
    Review
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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

7 authors.

Guangyao LvDepartment of Pharmacy, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Menglin YangQuality Management Department, Marine Biomedical Research Institute of Qingdao, Qingdao, China.
Keke GaiDepartment of Pharmacy, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Qiong JiaDepartment of Pharmacy, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Zhenzhen WangDepartment of Pharmacy, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Bin WangDepartment of Pharmacy, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Xueying LiSchool of Health, Binzhou Polytechnic, Binzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High mobility group box 1 (HMGB1) is a nuclear DNA-binding protein with a dual role in cancer, acting as an oncogene and a tumor suppressor. This protein regulates nucleosomal structure, DNA damage repair, and genomic stability within the cell, while also playing a role in immune cell functions. This review comprehensively evaluates the biological and clinical significance of HMGB1 in cancer, including its involvement in cell death and survival, its potential as a therapeutic target and cancer biomarker, and as a prosurvival signal for the remaining cells after exposure to cytotoxic anticancer treatments. We highlight the need for a better understanding of the cellular markers and mechanisms involved in the involvement of HMGB1in cancer, and aim to provide a deeper understanding of its role in cancer progression.

Indexed as

autophagycancerchemotherapy resistanceHMGB1immunotherapy

Identifiers

PMID38725632
PMCPMC11079206

What OpenQuestion holds

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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.