» Articles » PMID: 36032067

The Fra-1: Novel Role in Regulating Extensive Immune Cell States and Affecting Inflammatory Diseases

Overview
Journal Front Immunol
Date 2022 Aug 29
PMID 36032067
Authors
Affiliations
Soon will be listed here.
Abstract

Fra-1(Fos-related antigen1), a member of transcription factor activator protein (AP-1), plays an important role in cell proliferation, apoptosis, differentiation, inflammation, oncogenesis and tumor metastasis. Accumulating evidence suggest that the malignancy and invasive ability of tumors can be significantly changed by directly targeting Fra-1. Besides, the effects of Fra-1 are gradually revealed in immune and inflammatory settings, such as arthritis, pneumonia, psoriasis and cardiovascular disease. These regulatory mechanisms that orchestrate immune and non-immune cells underlie Fra-1 as a potential therapeutic target for a variety of human diseases. In this review, we focus on the current knowledge of Fra-1 in immune system, highlighting its unique importance in regulating tissue homeostasis. In addition, we also discuss the possible critical intervention strategy in diseases, which also outline future research and development avenues.

Citing Articles

Fra-1 affects chemotherapy sensitivity by inhibiting ferroptosis in gastric cancer cells.

Zeng F, Cao J, Chen Y, Tang J, He Q, Liao S Cancer Drug Resist. 2024; 7:44.

PMID: 39624082 PMC: 11609144. DOI: 10.20517/cdr.2024.101.


Saikosaponin A Recovers Impaired Filaggrin Levels in Inflamed Skin by Downregulating the Expression of FRA1 and c-Jun.

Ahn S, Yeo H, Jung E, Kim T, Han J, Han Lee Y Molecules. 2024; 29(17).

PMID: 39274912 PMC: 11396542. DOI: 10.3390/molecules29174064.


Blockade of the ADAM8-Fra-1 complex attenuates neuroinflammation by suppressing the Map3k4/MAPKs axis after spinal cord injury.

Qian Z, Li R, Zhao T, Xie K, Li P, Li G Cell Mol Biol Lett. 2024; 29(1):75.

PMID: 38755530 PMC: 11100242. DOI: 10.1186/s11658-024-00589-3.


Epigenetic and transcriptional responses in circulating leukocytes are associated with future decompensation during SARS-CoV-2 infection.

McClain M, Zhbannikov I, Satterwhite L, Henao R, Giroux N, Ding S iScience. 2024; 27(1):108288.

PMID: 38179063 PMC: 10765013. DOI: 10.1016/j.isci.2023.108288.


Identification of potential miR‑155 target genes in epidermal immune microenvironment of atopic dermatitis patients and their inflammatory effects on HaCaT cells.

Wang X, Chen L, Chen X, Liu C, Qiu W, Guo K Exp Ther Med. 2023; 27(1):25.

PMID: 38125354 PMC: 10728954. DOI: 10.3892/etm.2023.12313.


References
1.
Angel P, Karin M . The role of Jun, Fos and the AP-1 complex in cell-proliferation and transformation. Biochim Biophys Acta. 1991; 1072(2-3):129-57. DOI: 10.1016/0304-419x(91)90011-9. View

2.
Cook S, Aziz N, McMahon M . The repertoire of fos and jun proteins expressed during the G1 phase of the cell cycle is determined by the duration of mitogen-activated protein kinase activation. Mol Cell Biol. 1998; 19(1):330-41. PMC: 83891. DOI: 10.1128/MCB.19.1.330. View

3.
Meisner J, Song J, Price R . Arteriolar and venular remodeling are differentially regulated by bone marrow-derived cell-specific CX3CR1 and CCR2 expression. PLoS One. 2012; 7(9):e46312. PMC: 3454326. DOI: 10.1371/journal.pone.0046312. View

4.
Eferl R, Hasselblatt P, Rath M, Popper H, Zenz R, Komnenovic V . Development of pulmonary fibrosis through a pathway involving the transcription factor Fra-2/AP-1. Proc Natl Acad Sci U S A. 2008; 105(30):10525-30. PMC: 2492511. DOI: 10.1073/pnas.0801414105. View

5.
Wang J, Huo K, Ma L, Tang L, Li D, Huang X . Toward an understanding of the protein interaction network of the human liver. Mol Syst Biol. 2011; 7:536. PMC: 3261708. DOI: 10.1038/msb.2011.67. View