Zinc Finger E-Box Binding Homeobox 1 Regulates the Biological Behavior of Glioma Cells via iNOS/NF-κB Signaling

被引:0
作者
Cao, Jing [1 ]
Zhou, Haiyan [1 ]
Yang, Fan [1 ]
Fan, Duojiao [2 ]
Li, Hengzhou [1 ]
Fan, Tao [3 ]
Sun, Peng [1 ]
机构
[1] Baoding Second Hosp, Dept Emergency Med, Baoding City 071000, Hebei, Peoples R China
[2] Baoding Second Hosp, Dept Sci & Educ, Baoding City 071000, Hebei, Peoples R China
[3] Capital Med Univ, Dept Neurosurg, Beijing Sanbo Brain Hosp, Beijing 100093, Peoples R China
关键词
ZEB1; Glioma; NF-kappa B; iNOS; Proliferation; EMT; NONCODING RNA ZEB1-AS1; POOR-PROGNOSIS; EXPRESSION; PROGRESSION; RESISTANCE; GROWTH;
D O I
10.1166/jbt.2021.2549
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The gliomas pathogenesis is complex and effective molecular targets are still unclear. ZEB1 regulates epithelial mesenchymal transition (EMT) and participates in tumors. Our study intends to analyze ZEB1's role in glioma cells. qRT-PCR detected ZEB1 mRNA expression in normal group and tumor group. ZEB1 siRNA was transfected into glioma cells followed by measuring ZEB1, E-cadherin and Vimentin expression, cell proliferation, Capase-3 activity as well as NF-kappa B and iNOS changes by immunoblotting. Upregulation of ZEB1 was found in glioma tumor tissue and correlated with glioma clinicopathological characteristics. Interfering with ZEB1 by siRNA significantly down-regulated ZEB1, inhibited cell proliferation, increased Capase-3 activity, downregulated NF-kappa B and iNOS proteins in glioma cells, elevated E-cadherin and decreased Vimentin level (P < 0.05). ZEB1 downregulation in glioma cells can change the expression of NF-kappa B/iNOS, regulate cell apoptosis and inhibit cell proliferation, thereby delaying EMT process.
引用
收藏
页码:333 / 338
页数:6
相关论文
共 29 条
[1]   TNF-α Modulation of Intestinal Tight Junction Permeability Is Mediated by NIK/IKK-α Axis Activation of the Canonical NF-κB Pathway [J].
Al-Sadi, Rana ;
Guo, Shuhong ;
Ye, Dongmei ;
Rawat, Manmeet ;
Ma, Thomas Y. .
AMERICAN JOURNAL OF PATHOLOGY, 2016, 186 (05) :1151-1165
[2]   Integrated analysis of noncoding RNAs and mRNAs reveals their potential roles in the biological activities of the growth hormone receptor [J].
Chang, Lei ;
Qi, Haolong ;
Xiao, Yusha ;
Li, Changsheng ;
Wang, Yitao ;
Guo, Tao ;
Liu, Zhisu ;
Liu, Quanyan .
GROWTH HORMONE & IGF RESEARCH, 2016, 29 :11-20
[3]   Hypoxia-induced ZEB1 promotes cervical cancer progression via CCL8-dependent tumour-associated macrophage recruitment [J].
Chen, Xiao-Jing ;
Deng, Yuan-Run ;
Wang, Zi-Ci ;
Wei, Wen-Fei ;
Zhou, Chen-Fei ;
Zhang, Yan-Mei ;
Yan, Rui-Ming ;
Liang, Luo-Jiao ;
Zhong, Mei ;
Liang, Li ;
Wu, Sha ;
Wang, Wei .
CELL DEATH & DISEASE, 2019, 10 (7)
[4]   LncRNA-TP53TG1 Participated in the Stress Response Under Glucose Deprivation in Glioma [J].
Chen, Xin ;
Gao, Yang ;
Li, Deheng ;
Cao, Yiqun ;
Hao, Bin .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 118 (12) :4897-4904
[5]   A New Hope in Immunotherapy for Malignant Gliomas: Adoptive T Cell Transfer Therapy [J].
Chung, Dong-Sup ;
Shin, Hye-Jin ;
Hong, Yong-Kil .
JOURNAL OF IMMUNOLOGY RESEARCH, 2014, 2014
[6]   Tumor-associated macrophages (TAMs) depend on ZEB1 for their cancer-promoting roles [J].
Cortes, Marlies ;
Sanchez-Moral, Lidia ;
de Barrios, Oriol ;
Fernandez-Acenero, Maria J. ;
Martinez-Campanario, M. C. ;
Esteve-Codina, Anna ;
Darling, Douglas S. ;
Gyorffy, Balazs ;
Lawrence, Toby ;
Dean, Douglas C. ;
Postigo, Antonio .
EMBO JOURNAL, 2017, 36 (22) :3336-3355
[7]   LncRNA-XIST interacts with miR-29c to modulate the chemoresistance of glioma cell to TMZ through DNA mismatch repair pathway [J].
Du, Peng ;
Zhao, Haiting ;
Peng, Renjun ;
Liu, Qing ;
Yuan, Jian ;
Peng, Gang ;
Liao, Yiwei .
BIOSCIENCE REPORTS, 2017, 37
[8]   Cathepsin L upregulation-induced EMT phenotype is associated with the acquisition of cisplatin or paclitaxel resistance in A549 cells [J].
Han, Mei-ling ;
Zhao, Yi-fan ;
Tan, Cai-hong ;
Xiong, Ya-jie ;
Wang, Wen-juan ;
Wu, Feng ;
Fei, Yao ;
Wang, Long ;
Liang, Zhong-qin .
ACTA PHARMACOLOGICA SINICA, 2016, 37 (12) :1606-1622
[9]   LncRNA PLAC2 down-regulates RPL36 expression and blocks cell cycle progression in glioma through a mechanism involving STAT1 [J].
Hu, Yan-Wei ;
Kang, Chun-Min ;
Zhao, Jing-Jing ;
Nie, Ying ;
Zheng, Lei ;
Li, Hai-Xia ;
Li, Xin ;
Wang, Qian ;
Qiu, Yu-Rong .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2018, 22 (01) :497-510
[10]   iNOS: A Potential Therapeutic Target for Malignant Glioma [J].
Jahani-Asl, A. ;
Bonni, A. .
CURRENT MOLECULAR MEDICINE, 2013, 13 (08) :1241-1249