全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

经典Wnt通路与胶质瘤
Canonical Wnt Pathway and Glioma

DOI: 10.12677/ACM.2023.133431, PP. 3037-3041

Keywords: 胶质瘤,经典Wnt通路,β-连环蛋白,卷曲蛋白,低密度脂蛋白受体相关蛋白
Glioma
, Canonical Wnt Pathway, β-Catenin, FZD, Lrp

Full-Text   Cite this paper   Add to My Lib

Abstract:

脑胶质瘤(glioma)源于胶质细胞的胶质瘤是中枢神经系统最常见的原发性肿瘤。由于中国的胶质瘤患者预后差,死亡率高,在人群中进行有效的胶质瘤筛查和危险因素研究是实现早期诊断和治疗的有效手段。胶质瘤细胞中经典的Wnt通路的异常激活使Wnt/β相关蛋白通路被用作精确治疗胶质瘤的目标。经典的Wnt通路是调控胶质瘤细胞增殖和凋亡的关键通路,也是调控胶质瘤发病机制的重要通路。因此,研究经典的Wnt通路在胶质瘤中的机制对该疾病的诊断、治疗和预后具有重要的临床意义。
Gliomas derived from glial cells are the most common primary tumours of the central nervous system. Due to the poor prognosis and high mortality rate of glioma patients in China, effective glioma screening and risk factor studies in the population are an effective means to achieve early diagnosis and treatment. Aberrant activation of the classical Wnt pathway in glioma cells has led to the use of the Wnt/β-related protein pathway as a target for the precise treatment of gliomas. The classical Wnt pathway is a key pathway in the regulation of glioma cell proliferation and apoptosis, and an important pathway in the regulation of glioma pathogenesis. Therefore, studying the mechanisms of the classical Wnt pathway in glioma has important clinical significance for the diagnosis, treatment and prognosis of this disease.

References

[1]  Zeng, Y., Que, T., Lin, J., et al. (2019) Oncogenic ZEB2/miR-637/HMGA1 Signaling Axis Targeting Vimentin Pro-motes the Malignant Phenotype of Glioma. Nucleic Acids, 23, 769-782.
https://doi.org/10.1016/j.omtn.2020.12.029
[2]  Zanders, E.D., Svensson, F. and Bailey, D.S. (2019) Therapy for Glioblastoma: Is It Working? Drug Discovery Today, 24, 1193-1201.
https://doi.org/10.1016/j.drudis.2019.03.008
[3]  陈谦学. 胶质母细胞瘤诊疗研究进展[J]. 肿瘤防治研究, 2022, 49(11): 1103-1106.
[4]  Diaz, M., Jo, J., Smolkin, M., Ratcliffe, S.J. and Schiff, D. (2021) Risk of Venous Thromboembolism in Grade II-IV Gliomas as a Function of Molecular Subtype. Neurology, 96, e1063-e1069.
https://doi.org/10.1212/WNL.0000000000011414
[5]  Tabnak, P., Mafakheri, A., Haji Emsailpoor, Z., Kazemi, T. and Shekari, N. (2021) Regulatory Interplay between microRNAs and WNT Pathway in Glioma. Biomedicine & Pharmacotherapy, 143, Article ID: 112187.
https://doi.org/10.1016/j.biopha.2021.112187
[6]  Aman, A.J., Fulbright, A.N. and Parichy, D.M. (2018) Wnt/β-Catenin Regulates an Ancient Signaling Network during Zebrafish Scale Development. eLife, 7, e37001.
https://doi.org/10.7554/eLife.37001
[7]  Steinhart, Z. and Angers, S. (2018) Wnt Signaling in Development and Tissue Homeostasis. Development, 145, dev146589.
https://doi.org/10.1242/dev.146589
[8]  Nusse, R. and Clevers, H. (2017) Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities. Cell, 169, 985-999.
https://doi.org/10.1016/j.cell.2017.05.016
[9]  Clevers, H. and Nusse, R. (2012) Wnt/β-Catenin Signaling and Disease. Cell, 149, 1192-1205.
https://doi.org/10.1016/j.cell.2012.05.012
[10]  Zhang, J., Cai, H., Sun, L., Zhan, P., Chen, M., Zhang, F., Ran, Y. and Wan, J. (2018) LGR5, a Novel Functional Glioma Stem Cell Marker, Promotes EMT by Activating the Wnt/β-Catenin Pathway and Predicts Poor Survival of Glioma Patients. Journal of Experimental & Clinical Cancer Research, 37, Article No. 225.
https://doi.org/10.1186/s13046-018-0864-6
[11]  Hayat, R., Manzoor, M. and Hussain, A. (2022) Wnt Signaling Pathway: A Comprehensive Review. Cell Biology International, 46, 863-877.
https://doi.org/10.1002/cbin.11797
[12]  Sheng, J., He, X., Yu, W., Chen, Y., Long, Y., Wang, K., Zhu, S. and Liu, Q. (2021) P53-Targeted lncRNA ST7-AS1 Acts as a Tumour Suppressor by Interacting with PTBP1 to Suppress the Wnt/β-Catenin Signalling Pathway in Glioma. Cancer Letters, 503, 54-68.
https://doi.org/10.1016/j.canlet.2020.12.039
[13]  Wang, Z., Li, Z. and Ji, H. (2021) Direct Targeting of β-Catenin in the Wnt Signaling Pathway: Current Progress and Perspectives. Medicinal Research Reviews, 41, 2109-2129.
https://doi.org/10.1002/med.21787
[14]  Liu, K., Jiang, L., Shi, Y., Liu, B., He, Y., Shen, Q., Jiang, X., Nie, Z., Pu, J., Yang, C. and Chen, Y. (2022) Hypoxia-Induced GLT8D1 Promotes Glioma Stem Cell Maintenance by Inhibiting CD133 Degradation through N-Linked Glycosylation. Cell Death & Differentiation, 29, 1834-1849.
https://doi.org/10.1038/s41418-022-00969-2
[15]  Davidson, G. (2021) LRPs in WNT Signalling. In: Schulte, G. and Kozielewicz, P., Eds., Pharmacology of the WNT Signaling System. Handbook of Experimental Pharmacology, Vol. 269, Springer, Cham, 45-73.
https://doi.org/10.1007/164_2021_526
[16]  Jones, T.S. and Holland, E.C. (2012) Standard of Care Therapy for Malignant Glioma and Its Effect on Tumor and Stromal Cells. Oncogene, 31, 1995-2006.
https://doi.org/10.1038/onc.2011.398
[17]  Zhou, C., Zhang, Y., Dai, J., Zhou, M., Liu, M., Wang, Y., Chen, X.-Z. and Tang, J. (2016) Pygo2 Functions as a Prognostic Factor for Glioma due to Its up-Regulation of H3K4me3 and Promotion of MLL1/MLL2 Complex Recruitment. Scientific Reports, 6, Article No. 22066.
https://doi.org/10.1038/srep22066
[18]  Kaur, N., Chettiar, S., Rathod, S., Rath, P., Muzumdar, D., Shaikh, M.L. and Shiras, A. (2013) Wnt3a Mediated Activation of Wnt/β-Catenin Signaling Promotes Tumor Progression in Glioblastoma. Molecular and Cellular Neuroscience, 54, 44-57.
https://doi.org/10.1016/j.mcn.2013.01.001
[19]  Wu, W., Tian, Y., Wan, H., Song, Y., Li, J. and Zhang, L. (2013) The Expressions of Wnt/β-Catenin Pathway-Related Components in Brainstem Gliomas. Canadian Journal of Neuro-logical Sciences, 40, 355-360.
https://doi.org/10.1017/S031716710001430X
[20]  Denysenko, T., Annovazzi, L., Cassoni, P., Melcarne, A., Mellai, M. and Schiffer, D. (2016) WNT/β-Catenin Signaling Pathway and Downstream Modulators in Low- and High-Grade Glioma. Cancer Genomics & Proteomics, 13, 31-45.
[21]  杨烽. 脑胶质瘤信号通路的研究进展(综述) [J]. 安徽医专学报, 2022, 21(4): 77-79+82.
[22]  陈静, 董善武, 陈咏丽, 陈海珊, 蒋姝, 陈澄, 罗超. miR-640通过抑制SLIT1介导Wnt/β-catenin通路促进脑胶质瘤对替莫唑胺的耐药[J]. 肿瘤学杂志, 2022, 28(7): 568-573.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133