国际医药卫生导报 ›› 2023, Vol. 29 ›› Issue (2): 183-.DOI: 10.3760/cma.j.issn.1007-1245.2023.02.009

• 科研课题专栏 • 上一篇    下一篇

XBP1Twist1VEGF在人脑胶质瘤中的表达及临床意义

周保丹  高飞  王淇民  王明国   

  1. 南阳市第二人民医院神经外科,南阳 473000

  • 出版日期:2023-01-15 发布日期:2023-01-30
  • 通讯作者: 周保丹,Email:zhoubd228@163.com
  • 基金资助:

    河南省医学科技攻关计划项目(LHGJ20191471

Expressions and clinical significance of XBP1, Twist1, and VEGF protein in human glioma 

Zhou Baodan, Gao Fei, Wang Qimin, Wang Mingguo   

  1. Department of Neurosurgery, The Second People's Hospital of Nanyang City, Nanyang 473000, China

  • Online:2023-01-15 Published:2023-01-30
  • Contact: Zhou Baodan, Email: zhoubd228@163.com
  • Supported by:

    Project of Problem-tackling Plan of Medical Science and Technology in Henan (LHGJ20191471)

摘要:

目的 探讨X盒结合蛋白1XBP1)、Twist相关蛋白1Twist1)、血管内皮生长因子(VEGF)在人脑胶质瘤中的表达及临床意义。方法 选取20189月至20206月南阳市第二人民医院保存的50份脑胶质瘤组织作为研究对象,其中男性28例,女性22例,年龄(37.66±5.66)岁,根据预后将其分为生存组和死亡组。同时选取40份正常脑组织作为对照组,男性24例,女性16例,年龄(37.75±7.68)岁。检测各组组织XBP1Twist1VEGF阳性表达;分析其与临床病理特征的相关性;采用logistic回归分析影响患者预后的危险因素;Kaplan-Meier进行生存分析。结果 与对照组相比,生存组和死亡组XBP1Twist1VEGF阳性表达均较高(χ2=57.27055.35055.589,均P<0.05);XBP1Twist1VEGF与患者组织分化(χ2=6.34910.9388.140P=0.0120.0010.004)、临床分期(χ2=4.5048.2956.062P=0.0340.0040.014)以及Karnofsky功能状态评分(χ2=8.3334.6886.527P=0.0040.0670.011)有显著相关性;XBP1Twist1VEGF均是影响患者预后的危险因素(均P<0.05);与XBP1Twist1VEGF阴性表达相比,阳性表达患者的生存时间较短,均P<0.05结论 XBP1Twist1VEGF与脑胶质瘤患者临床病理特征、预后及生存有一定的相关性。

关键词:

XBP1, Twist1, VEGF, 脑胶质瘤

Abstract:

Objective To investigate the expression and clinical significance of X-box binding protein 1 (XBP1), Twist related protein 1 (Twist1), and vascular endothelial growth factor (VEGF) in human glioma. Methods Fifty cases of glioma tissue preserved in The Second People's Hospital of Nanyang City from September 2018 to June 2020 were selected; of which, 28 cases were male and 22 cases were female, with an age of (37.66±5.66) years; they were divided into a survived group and a death group according to their prognosis. Forty cases of normal brain tissue were selected as a control group, including 24 males and 16 females who were (37.75±7.68) years old. The positive expressions of XBP1, Twist1, and VEGF in the tissues of both groups were detected. Their correlations with clinicopathological features were analyzed. The logistic regression analysis was used to analyze the risk factors affecting patient prognosis. Kaplan-Meier was used for survival analysis. Results The positive expressions of XBP1, Twist1, and VEGF in the survived group and the death group were higher than those in the control group (χ2=57.270, 55.350, and 55.589; all P<0.05). XBP1, Twist1, and VEGF were associated with the patients' tissue differentiation (χ2=6.349, 10.938, and 8.140; P=0.012, 0.001, and 0.004), clinical stage (χ2=4.504, 8.295, and 6.062; P=0.034, 0.004, and 0.014), and Karnofsky Performance Status score (χ2=8.333, 4.688, and 6.527; P=0.004, 0.067, and 0.011); XBP1, Twist1, and VEGF were risk factors affecting the patients' prognosis (all P<0.05); the patients with positive expressions of XBP1, Twist1, and VEGF had shorter survival time than those with negative expressions (all P<0.05). Conclusion XBP1, Twist1, and VEGF have certain correlations with clinicopathological features, prognosis, and survival of glioma patients.

Key words:

XBP1, Twist1, VEGF, Glioma