TXNIP公司
硫氧还蛋白相互作用蛋白
癌症研究
前列腺癌
细胞凋亡
硫氧还蛋白
癌症
生物
过剩1
细胞周期
抑制器
内分泌学
生物化学
遗传学
葡萄糖摄取
氧化应激
胰岛素
作者
Ming Xie,Ruiyan Xie,Sen Xie,Yiyi Wu,Wei Wang,Xiang Li,Yuanyu Xu,Bo Liu,Yu Zhou,Tao Wang,Lei Gao,Tiejun Pan
摘要
Abstract Prostate cancer (PCa) is one of the most common malignant tumors in the world. Thioredoxin interacting protein (TXNIP) is downregulated in a variety of human tumors and plays an important role in tumor suppression. However, the expression level and biological functions of TXNIP in PCa have not been identified yet. Therefore, this study aims to investigate the expression and biological functions of TXNIP in PCa. We reported that the expression of TXNIP was significantly decreased in PCa and associated with clinicopathological features. Overexpression of TXNIP could significantly inhibited PC‐3 cells proliferation, migration, invasion, and glucose uptake. Additionally, overexpression of TXNIP could remarkably block cell cycle in the G0/G1 phase and promoted cell apoptosis. Furthermore, TXNIP expression correlated inversely with GLUT1 expression in PCa. Taken together, our results for the first time revealed that TXNIP was decreased in PCa. Moreover, TXNIP might act as a tumor suppressor of PCa and correlated with tumor occurrence and development. Our findings cast a new light on better understanding the occurrence and development of PCa and indicated that TXNIP might be favorable for PCa molecular target therapy.
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