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硫氧还蛋白相互作用蛋白在癌症和糖尿病中的作用

Thioredoxin-Interacting Protein in Cancer and Diabetes.

机构信息

Department of Clinical Laboratory Sciences, Tenri Health Care University, Tenri, Japan.

Department of Infection and Prevention, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan.

出版信息

Antioxid Redox Signal. 2022 May;36(13-15):1001-1022. doi: 10.1089/ars.2021.0038. Epub 2021 Oct 7.

Abstract

Thioredoxin-interacting protein (Txnip) is an α-arrestin protein that acts as a cancer suppressor. Txnip is simultaneously a critical regulator of energy metabolism. Other alpha-arrestin proteins also play key roles in cell biology and cancer. Txnip expression is regulated by multilayered mechanisms, including transcriptional regulation, microRNA, messenger RNA (mRNA) stabilization, and protein degradation. The Txnip-based connection between cancer and metabolism has been widely recognized. Meanwhile, new aspects are proposed for the mechanism of action of Txnip, including the regulation of RNA expression and autophagy. Arrestin domain containing 3 (ARRDC3), another α-arrestin protein, regulates endocytosis and signaling, whereas ARRDC1 and ARRDC4 regulate extracellular vesicle formation. The mechanism of action of Txnip is yet to be elucidated. The regulation of intracellular protein trafficking by arrestin family proteins has opened an emerging field of biology and medical research, which needs to be examined further. A fundamental understanding of the mechanism of action of Txnip and other arrestin family members needs to be explored in the future to combat diseases such as cancer and diabetes. . 36, 1001-1022.

摘要

硫氧还蛋白相互作用蛋白(Txnip)是一种 α-抑制蛋白,作为一种肿瘤抑制因子。Txnip 同时也是能量代谢的关键调节剂。其他 α-抑制蛋白也在细胞生物学和癌症中发挥关键作用。Txnip 的表达受多层次机制调控,包括转录调控、微小 RNA、信使 RNA(mRNA)稳定和蛋白降解。基于 Txnip 的癌症与代谢之间的联系已得到广泛认可。同时,提出了 Txnip 作用机制的新方面,包括 RNA 表达和自噬的调节。另一种 α-抑制蛋白 arrestin 结构域包含 3(ARRDC3)调节内吞作用和信号转导,而 ARRDC1 和 ARRDC4 调节细胞外囊泡的形成。Txnip 的作用机制尚待阐明。抑制蛋白家族蛋白对细胞内蛋白运输的调节开辟了一个新兴的生物学和医学研究领域,需要进一步研究。未来需要深入研究 Txnip 和其他抑制蛋白家族成员的作用机制,以对抗癌症和糖尿病等疾病。36, 1001-1022。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca9/9125520/55aca3118f43/ars.2021.0038_figure1.jpg

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