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Expression and function of FRA1 protein in tumors
Xiaoyan Jiang1, Hui Xie1, Yingyu Dou1
1Department of Gynecology and Obstetrics, The Third Xiangya Hospital of Central South University, 138 Tong zipo Rd, Yuelu District, Changsha, 410013, China.
Abstract:
AP-1 is a dimeric complex that is composed of JUN, FOS, ATF and MAF protein families. FOS-related antigen 1 (FRA1) which encoded by FOSL1 gene, belongs to the FOS protein family, and mainly forms an AP-1 complex with the protein of the JUN family to exert an effect. Regulation of FRA1 occurs at levels of transcription and post-translational modification, and phosphorylation is the major post-translational modification. FRA1 is mainly regulated by the mitogen-activated protein kinases signaling pathway and is degraded by ubiquitin-independent proteasomes. FRA1 can affect biological functions, such as tumor proliferation, differentiation, invasion and apoptosis. Studies have demonstrated that FRA1 is abnormally expressed in many tumors and plays a relevant role, but the specific condition varies from the target organs. FRA1 is overexpressed in breast cancer, lung cancer, colorectal cancer, prostate cancer, nasopharyngeal cancer, thyroid cancer and other tumors. However, the expression of FRA1 is decreased in cervical cancer, and the expression of FRA1 in ovarian cancer and oral squamous cell carcinoma is still controversial. In this review, we present a detailed description of the regulatory factors and functions of FRA1, also, the expression of FRA1 in various tumors and its function in relative tumor.
Insights
FOS-related antigen 1 (FRA1) is a key protein in tumor progression, affecting proliferation and invasion. Its expression varies across cancers, being overexpressed in many but decreased in others, highlighting its complex role.
Area of Science:
- Molecular Biology
- Oncology
Background:
- AP-1 is a transcription factor complex involving JUN, FOS, ATF, and MAF protein families.
- FOS-related antigen 1 (FRA1), encoded by FOSL1, is a crucial component of the AP-1 complex, primarily partnering with JUN proteins.
Purpose of the Study:
- To review the regulatory mechanisms of FRA1.
- To elucidate the diverse roles of FRA1 in various human cancers.
- To summarize FRA1 expression patterns in different tumor types.
Main Methods:
- Literature review of studies on FRA1 regulation and function.
- Analysis of FRA1 expression data across multiple cancer types.
- Synthesis of information on FRA1's impact on tumor biology.
Main Results:
- FRA1 is regulated transcriptionally and post-translationally, with phosphorylation being a major modification.
- Mitogen-activated protein kinase (MAPK) signaling pathways significantly influence FRA1 regulation and degradation.
- FRA1 overexpression is observed in breast, lung, colorectal, prostate, nasopharyngeal, and thyroid cancers, correlating with tumor progression.
- Conversely, FRA1 expression is decreased in cervical cancer, with controversial findings in ovarian and oral cancers.
Conclusions:
- FRA1 plays a significant role in tumor proliferation, differentiation, invasion, and apoptosis.
- The expression and function of FRA1 are context-dependent, varying by tumor type and organ.
- Understanding FRA1's dysregulation is critical for developing targeted cancer therapies.
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