TXNIP公司
硫氧还蛋白相互作用蛋白
胰岛素抵抗
糖尿病
胰岛素
细胞凋亡
医学
硫氧还蛋白
下调和上调
内分泌学
癌症研究
生物
内科学
细胞生物学
化学
氧化应激
生物化学
基因
作者
Rajesh Basnet,Til Bahadur Basnet,Buddha Bahadur Basnet,Sandhya Khadka
标识
DOI:10.2174/1389450123666220303092324
摘要
Background: Diabetes mellitus (DM) is a common metabolic disorder characterized by a persistent increment of blood glucose. Type 2 DM is characterized by insulin resistance and β-cell dysfunction. Thioredoxin-interacting protein (TXNIP) is among the factors that control the produc-tion and loss of pancreatic β-cells. Objective: Recent studies have shown that high glucose can significantly up-regulate the expression of the TXNIP. Overexpression of TXNIP in β-cells not only induced apoptosis but also decreased the production of insulin. At the same time, TXNIP deficiency protected the apoptosis of β-cells, leading to increased insulin production. Therefore, finding small molecules that can modulate TXNIP expression and downstream signalling pathways is essential. Thus, the inhibition of TXNIP has beneficial effects on the cardiovascular system and other tissues such as the heart and the kid-ney in DM. Therefore, DM treatment must target small TXNIP activity, inhibit expression, and promote endogenous cell mass and insulin production. Conclusion: This review briefly describes the effect mechanism, regulatory mechanism, and crystal structure of TXNIP. In addition, we highlight how TXNIP signalling networks contribute to diabe-tes and interact with drugs that inhibit the development often and its complexes. Finally, the current status and prospects of TXNIP targeted therapy are also discussed.
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