Literature DB >> 33140586

The performance of the alarmin HMGB1 in pediatric diseases: From lab to clinic.

Bo Li1, Xin Peng2, He Li3, Fei Chen4, Yuxia Chen5, Yingqian Zhang1, Kai Le6.   

Abstract

INTRODUCTION: The ubiquitously expressed nonhistone nuclear protein high-mobility group box protein 1 (HMGB1) has different functions related to posttranslational modifications and cellular localization. In the nucleus, HMGB1 modulates gene transcription, replication and DNA repair as well as determines chromosomal architecture. When the post-transcriptional modified HMGB1 is released into the extracellular space, it triggers several physiological and pathological responses and initiates innate immunity through interacting with its reciprocal receptors (i.e., TLR4/2 and RAGE). The effect of HMGB1-mediated inflammatory activation on different systems has received increasing attention. HMGB1 is now considered to be an alarmin and participates in multiple inflammation-related diseases. In addition, HMGB1 also affects the occurrence and progression of tumors. However, most studies involving HMGB1 have been focused on adults or mature animals. Due to differences in disease characteristics between children and adults, it is necessary to clarify the role of HMGB1 in pediatric diseases. METHODS AND
RESULTS: Through systematic database retrieval, this review aimed to first elaborate the characteristics of HMGB1 under physiological and pathological conditions and then discuss the clinical significance of HMGB1 in the pediatric diseases according to different systems.
CONCLUSIONS: HMGB1 plays an important role in a variety of pediatric diseases and may be used as a diagnostic biomarker and therapeutic target for new strategies for the prevention and treatment of pediatric diseases.
© 2020 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd.

Entities:  

Keywords:  HMGB1; clinic; inflammation; laboratory; pediatric

Year:  2020        PMID: 33140586     DOI: 10.1002/iid3.370

Source DB:  PubMed          Journal:  Immun Inflamm Dis        ISSN: 2050-4527


  5 in total

1.  HMGB1: A Potential Target of Nervus Vagus Stimulation in Pediatric SARS-CoV-2-Induced ALI/ARDS.

Authors:  Lina Jankauskaite; Mantas Malinauskas; Goda-Camille Mickeviciute
Journal:  Front Pediatr       Date:  2022-05-11       Impact factor: 3.569

2.  Exosomal HMGB1 derived from hypoxia-conditioned bone marrow mesenchymal stem cells increases angiogenesis via the JNK/HIF-1α pathway.

Authors:  Wenling Gao; Ronghan He; Jianhua Ren; Wenhui Zhang; Kun Wang; Lei Zhu; Tangzhao Liang
Journal:  FEBS Open Bio       Date:  2021-04-01       Impact factor: 2.693

Review 3.  High Mobility Group Box 1: Biological Functions and Relevance in Oxidative Stress Related Chronic Diseases.

Authors:  Simona Taverna; Alessandro Tonacci; Maria Ferraro; Giuseppe Cammarata; Giuseppina Cuttitta; Salvatore Bucchieri; Elisabetta Pace; Sebastiano Gangemi
Journal:  Cells       Date:  2022-03-01       Impact factor: 6.600

4.  Oxidized high mobility group B-1 enhances metastability of colorectal cancer via modification of mesenchymal stem/stromal cells.

Authors:  Shingo Kishi; Rina Fujiwara-Tani; Kanya Honoki; Rika Sasaki; Shiori Mori; Hitoshi Ohmori; Takamitsu Sasaki; Yoshihiro Miyagawa; Isao Kawahara; Akira Kido; Yasuhito Tanaka; Hiroki Kuniyasu
Journal:  Cancer Sci       Date:  2022-05-23       Impact factor: 6.518

5.  Fecal High-Mobility Group Box 1 as a Marker of Early Stage of Necrotizing Enterocolitis in Preterm Neonates.

Authors:  Roberta Vitali; Gianluca Terrin; Francesca Palone; Ilaria Laudadio; Salvatore Cucchiara; Giovanni Boscarino; Maria Di Chiara; Laura Stronati
Journal:  Front Pediatr       Date:  2021-06-10       Impact factor: 3.418

  5 in total

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