Tissue thioredoxin-interacting protein expression predicted recurrence in patients with meningiomas
Tissue thioredoxin-interacting protein expression predicted recurrence in patients with meningiomas
复制标题
组织硫氧还蛋白相互作用蛋白表达预测脑膜瘤患者的复发
DOI:
10.1007/s10147-017-1103-4
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发表时间:
2017-08-01
影响因子:
3.3
通讯作者:
Hu, Guohan
中科院分区:
文献类型:
--
作者:
Cai, Zheng;Zhang, Chenran;Hu, Guohan
Background The redox regulatory protein, thioredoxin-interacting protein (TXNIP), has been confirmed as an important tumor suppressor gene in various types of human cancers. In previous studies, we found that overexpression of tumor suppressor gene RIZ1 in meningiomas can significantly improve the expression of TXNIP by microarray data analysis. Therefore, we hypothesized that TXNIP was associated with the initiation and progression of meningiomas.Methods First, we evaluated the expression of TXNIP and Ki-67 in meningioma tissues from 65 patients using immunohistochemistry. We also analyzed the correlation between TXNIP immunoreactivity and clinicopathological features, as well as patient prognostic factors.Results According to immunohistochemistry results, high-grade meningioma tissues had significantly lower expression of TXNIP than benign meningioma tissues (29.31 +/- 18.70 vs 74.61 +/- 7.51, P < 0.0001). TXNIP and Ki67 were negatively correlated (P < 0.0001). Moreover, the expression of TXNIP was higher in nonrecurrent high-grade meningiomas (P < 0.05). In addition, Kaplan-Meier analysis indicated that expression of TXNIP and Ki-67 was related to recurrence-free time. Multivariate Cox analysis showed that TXNIP expression level was the only independent predictor for meningioma prognosis.Conclusion Our results demonstrated that high expression of TXNIP indicates a lower pathological grade of meningnioma, and is also associated with longer recurrence-free time. Therefore, TXNIP could be regarded as a potential molecular marker to predict recurrence in patients with meningiomas.