Chen Yiting, Ning Jieling, Cao Wenjie, Wang Shuanglian, Du Tao, Jiang Jiahui, Feng Xueping, Zhang Bin
Department of Oncology and Institute of Medical Sciences, National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
Department of Histology and Embryology, Xiangya School of Medicine, Central South University, Changsha, China.
Front Oncol. 2020 Oct 21;10:568574. doi: 10.3389/fonc.2020.568574. eCollection 2020.
Thioredoxin-interacting protein (TXNIP) is a thioredoxin-binding protein that can mediate oxidative stress, inhibit cell proliferation, and induce apoptosis by inhibiting the function of the thioredoxin system. TXNIP is important because of its wide range of functions in cardiovascular diseases, neurodegenerative diseases, cancer, diabetes, and other diseases. Increasing evidence has shown that TXNIP expression is low in tumors and that it may act as a tumor suppressor in various cancer types such as hepatocarcinoma, breast cancer, and lung cancer. TXNIP is known to inhibit the proliferation of breast cancer cells by affecting metabolic reprogramming and can affect the invasion and migration of breast cancer cells through the TXNIP-HIF1α-TWIST signaling axis. TXNIP can also prevent the occurrence of bladder cancer by inhibiting the activation of ERK, which inhibits apoptosis in bladder cancer cells. In this review, we find that TXNIP can be regulated by binding to transcription factors or other binding proteins and can also be downregulated by epigenetic changes or miRNA. In addition, we also summarize emerging insights on TXNIP expression and its functional role in different kinds of cancers, as well as clarify its participation in metabolic reprogramming and oxidative stress in cancer cells, wherein it acts as a putative tumor suppressor gene to inhibit the proliferation, invasion, and migration of different tumor cells as well as promote apoptosis in these cells. TXNIP may therefore be of basic and clinical significance for finding novel molecular targets that can facilitate the diagnosis and treatment of malignant tumors.
硫氧还蛋白相互作用蛋白(TXNIP)是一种硫氧还蛋白结合蛋白,它可以介导氧化应激,抑制细胞增殖,并通过抑制硫氧还蛋白系统的功能诱导细胞凋亡。TXNIP因其在心血管疾病、神经退行性疾病、癌症、糖尿病和其他疾病中的广泛功能而重要。越来越多的证据表明,TXNIP在肿瘤中的表达较低,并且它可能在各种癌症类型(如肝癌、乳腺癌和肺癌)中作为肿瘤抑制因子发挥作用。已知TXNIP通过影响代谢重编程来抑制乳腺癌细胞的增殖,并可通过TXNIP-HIF1α-TWIST信号轴影响乳腺癌细胞的侵袭和迁移。TXNIP还可以通过抑制ERK的激活来预防膀胱癌的发生,而ERK的激活会抑制膀胱癌细胞的凋亡。在本综述中,我们发现TXNIP可以通过与转录因子或其他结合蛋白结合来调节,也可以通过表观遗传变化或miRNA下调。此外,我们还总结了关于TXNIP在不同类型癌症中的表达及其功能作用的新见解,并阐明了其在癌细胞代谢重编程和氧化应激中的参与情况,其中它作为一种假定的肿瘤抑制基因,抑制不同肿瘤细胞的增殖、侵袭和迁移,并促进这些细胞的凋亡。因此,TXNIP对于寻找有助于恶性肿瘤诊断和治疗的新型分子靶点可能具有基础和临床意义。