Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Severance Biomedical Science Institute and Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Korea.
Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Severance Biomedical Science Institute and Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Korea; Chronic Intractable Disease Systems Medicine Research Center, Institute of Genetic Science, Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Korea.
BMB Rep. 2022 Aug;55(8):380-388. doi: 10.5483/BMBRep.2022.55.8.092.
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].
B 细胞易位基因 1(BTG1)和 BTG2 通过调节转录、转录后和翻译等多种核心生物学步骤,在包括增殖、凋亡和细胞生长在内的广泛细胞活动中发挥关键作用。BTG1 和 BTG2 已通过 B 细胞白血病和多种淋巴瘤类型的基因组分析得到鉴定,这两种基因在这些肿瘤中通常发生突变,这表明它们作为肿瘤抑制因子发挥作用。此外,实体肿瘤中 BTG1 或 BTG2 的低表达水平常与恶性进展和不良治疗结果相关。从生理角度来看,BTG1 和 BTG2 已被发现对造血谱系(如造血干细胞[HSCs]和幼稚 T 细胞和记忆 T 细胞)的静止状态具有关键调节功能,突出了它们在维持静止状态中的新作用。总之,最近研究中的新证据表明,BTG1 和 BTG2 在各种组织和细胞中发挥核心的抗增殖作用,表明它们具有作为创新治疗靶点的潜力。[BMB 报告 2022;55(8):380-388]。