Research Progress of TXNIP as a Tumor Suppressor Gene Participating in the Metabolic Reprogramming and Oxidative Stress of Cancer Cells in Various Cancers.
Research Progress of TXNIP as a Tumor Suppressor Gene Participating in the Metabolic Reprogramming and Oxidative Stress of Cancer Cells in Various Cancers.
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TXNIP作为抑癌基因参与多种癌症中癌细胞代谢重编程和氧化应激的研究进展
DOI:
10.3389/fonc.2020.568574
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发表时间:
2020
影响因子:
4.7
通讯作者:
Zhang B
中科院分区:
文献类型:
--
作者:
Chen Y;Ning J;Cao W;Wang S;Du T;Jiang J;Feng X;Zhang B
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.
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影响因子:
3.8
作者:
Daoud, Afra Z.;Mulholland, Eoghan J.;McCarthy, Helen O.
通讯作者:
McCarthy, Helen O.
影响因子:
9.7
作者:
Chen, Qiong;Liu, Tao;Wang, Linhui
通讯作者:
Wang, Linhui
影响因子:
5.7
作者:
Feingold PL;Surman DR;Brown K;Xu Y;McDuffie LA;Shukla V;Reardon ES;Crooks DR;Trepel JB;Lee S;Lee MJ;Gao S;Xi S;McLoughlin KC;Diggs LP;Beer DG;Nancarrow DJ;Neckers LM;Davis JL;Hoang CD;Hernandez JM;Schrump DS;Ripley RT
通讯作者:
Ripley RT
影响因子:
3.7
作者:
Devi TS;Hosoya K;Terasaki T;Singh LP
通讯作者:
Singh LP
影响因子:
--
作者:
Chen D;Dang BL;Huang JZ;Chen M;Wu D;Xu ML;Li R;Yan GR
通讯作者:
Yan GR