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Emerging role of anti-proliferative protein BTG1 and BTG2

Authors
 Sang Hyeon Kim  ;  In Ryeong Jung  ;  Soo Seok Hwang 
Citation
 BMB REPORTS, Vol.55(8) : 380-388, 2022-08 
Journal Title
BMB REPORTS
ISSN
 1976-6696 
Issue Date
2022-08
MeSH
Cell Cycle ; Cell Proliferation ; Humans ; Immediate-Early Proteins* / genetics ; Immediate-Early Proteins* / metabolism ; Neoplasm Proteins* / genetics ; Neoplasms* / genetics ; Tumor Suppressor Proteins* / genetics ; Tumor Suppressor Proteins* / metabolism
Abstract
The B cell translocation gene 1 (BTG1) and BTG2 play a key role in a wide range of cellular activities including proliferation, apoptosis, and cell growth via modulating a variety of central biological steps such as transcription, post-transcriptional, and translation. BTG1 and BTG2 have been identified by genomic profiling of B-cell leukemia and diverse lymphoma types where both genes are commonly mutated, implying that they serve as tumor suppressors. Furthermore, a low expression level of BTG1 or BTG2 in solid tumors is frequently associated with malignant progression and poor treatment outcomes. As physiological aspects, BTG1 and BTG2 have been discovered to play a critical function in regulating quiescence in hematopoietic lineage such as Hematopoietic stem cells (HSCs) and naïve and memory T cells, highlighting their novel role in maintaining the quiescent state. Taken together, emerging evidence from the recent studies suggests that BTG1 and BTG2 play a central anti-proliferative role in various tissues and cells, indicating their potential as targets for innovative therapeutics. [BMB Reports 2022; 55(8): 380-388].
Files in This Item:
T202205071.pdf Download
DOI
10.5483/BMBRep.2022.55.8.092
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers
Yonsei Authors
Hwang, Soo Seok(황수석)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/191782
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