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Published on: September 22, 2019
Pathophysiological role of BACH transcription factors in digestive system diseases
Qianben Song1,2, Xin Mao1,2, Mengjia Jing1,2
1Department of Gastroenterology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Abstract:
BTB and CNC homologous (BACH) proteins, including BACH1 and BACH2, are transcription factors that are widely expressed in human tissues. BACH proteins form heterodimers with small musculoaponeurotic fibrosarcoma (MAF) proteins to suppress the transcription of target genes. Furthermore, BACH1 promotes the transcription of target genes. BACH proteins regulate physiological processes, such as the differentiation of B cells and T cells, mitochondrial function, and heme homeostasis as well as pathogenesis related to inflammation, oxidative-stress damage caused by drugs, toxicants, or infections; autoimmunity disorders; and cancer angiogenesis, epithelial-mesenchymal transition, chemotherapy resistance, progression, and metabolism. In this review, we discuss the function of BACH proteins in the digestive system, including the liver, gallbladder, esophagus, stomach, small and large intestines, and pancreas. BACH proteins directly target genes or indirectly regulate downstream molecules to promote or inhibit biological phenomena such as inflammation, tumor angiogenesis, and epithelial-mesenchymal transition. BACH proteins are also regulated by proteins, miRNAs, LncRNAs, labile iron, and positive and negative feedback. Additionally, we summarize a list of regulators targeting these proteins. Our review provides a reference for future studies on targeted drugs in digestive diseases.
Insights
BTB and CNC homologous (BACH) proteins regulate gene transcription and cellular processes. This review focuses on BACH protein functions in the digestive system and their role in diseases like cancer and inflammation.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- BTB and CNC homologous (BACH) proteins, including BACH1 and BACH2, are transcription factors crucial for cellular regulation.
- They heterodimerize with small musculoaponeurotic fibrosarcoma (MAF) proteins to modulate gene transcription.
- BACH proteins influence diverse physiological processes and are implicated in various pathologies.
Purpose of the Study:
- To review the multifaceted roles of BACH proteins within the human digestive system.
- To elucidate the mechanisms by which BACH proteins regulate digestive system functions and diseases.
- To identify regulators of BACH proteins for potential therapeutic targeting in digestive diseases.
Main Methods:
- Literature review of studies on BACH proteins.
- Analysis of BACH protein interactions and regulatory networks.
- Synthesis of information on BACH protein involvement in digestive system physiology and pathology.
Main Results:
- BACH proteins play significant roles in the liver, gallbladder, esophagus, stomach, intestines, and pancreas.
- They directly and indirectly regulate genes involved in inflammation, angiogenesis, and epithelial-mesenchymal transition.
- BACH proteins are modulated by various factors including proteins, miRNAs, LncRNAs, and iron.
Conclusions:
- BACH proteins are key regulators in the digestive system, impacting both normal function and disease development.
- Understanding BACH protein regulation offers potential for targeted drug development for digestive diseases.
- Further research into BACH protein networks is warranted for therapeutic advancements.
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