[1]夏小超,王子豪,熊平,等.Notch信号通路在胶质瘤中作用的研究进展[J].中国临床神经外科杂志,2024,29(11):686-689.[doi:10.13798/j.issn.1009-153X.2024.11.011]
 XIA Xiao-chao,WANG Zi-hao,XIONG Ping,et al.Research advances on the function of Notch signaling pathway in glioma[J].,2024,29(11):686-689.[doi:10.13798/j.issn.1009-153X.2024.11.011]
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Notch信号通路在胶质瘤中作用的研究进展()
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《中国临床神经外科杂志》[ISSN:1009-153X/CN:42-1603/TN]

卷:
29
期数:
2024年11期
页码:
686-689
栏目:
综述
出版日期:
2024-11-30

文章信息/Info

Title:
Research advances on the function of Notch signaling pathway in glioma
文章编号:
1009-153X(2024)11-0686-04
作者:
夏小超王子豪熊平宋旅萌程银川李舜
637000四川南充,川北医学院附属医院神经外科(夏小超、王子豪、熊平、宋旅萌、程银川、李舜)
Author(s):
XIA Xiao-chao WANG Zi-hao XIONG Ping SONG Lü-meng CHENG Yin-chuan LI Shun
Department of Neurosurgery, Affiliated Hospital of North Sichuan Medical College, Nanchong 637000, China
关键词:
胶质瘤Notch信号通路肿瘤微环境肿瘤干细胞
Keywords:
Notch signaling pathway glioma Tumor Microenvironment Tumor stem cells
分类号:
R 739.41
DOI:
10.13798/j.issn.1009-153X.2024.11.011
文献标志码:
A
摘要:
Notch信号通路是一条重要的细胞信号传导途径。Notch受体经历三次切割后转位到细胞核,调节靶基因的转录,参与多种组织器官的发育和稳态。Notch信号通路异常与肿瘤发生、发展密切相关。研究表明,Notch信号通路在胶质瘤中的异常激活促进肿瘤细胞增殖、侵袭,影响肿瘤微环境和维持干细胞稳态。因此,有学者认为Notch信号通路可能是胶质瘤一种潜在的治疗靶点。有研究报道抑制Notch信号通路治疗胶质瘤,但这些药物的疗效有待商榷。近年来,随着Notch信号通路在胶质瘤中研究的不断深入,其有望为胶质瘤的治疗提供新的思路。本文就Notch信号通路在胶质瘤中的作用机制及其研究进展进行综述。
Abstract:
The Notch signaling pathway, functioning as a critical intercellular signaling conduit, exerts a vital role in the development and homeostasis maintenance of diverse tissues and organs. Once the Notch receptor undergoes three proteolytic cleavages, its intracellular domain (NICD) translocates to the nucleus and governs the transcriptional expression of a series of target genes. Researches conducted in recent years have indicated that the aberrant activation of the Notch signaling pathway is closely associated with the genesis and progression of tumors, particularly in glioma. The excessive activation of the Notch signaling pathway not only promotes the proliferation and invasion of tumor cells but also influences the tumor microenvironment and maintains the homeostasis of glioma stem cells. Consequently, the Notch signaling pathway is regarded as one of the potential therapeutic targets for glioma. Despite the fact that there have been studies reporting the treatment of glioma by inhibiting the Notch signaling pathway, the clinical efficacy of existing drugs still requires further validation. With the in-depth investigation of the mechanism of the Notch signaling pathway in glioma, this pathway is anticipated to offer novel strategies and notions for the treatment of glioma. This article will review the mechanism of the Notch signaling pathway in glioma and its latest research advancements.

参考文献/References:

[1] WANG Z, ZHANG H, XU S, et al. The adaptive transition of glioblastoma stem cells and its implications on treatments [J]. Signal Transduct Target Ther, 2021, 6(1): 124.
[2] CONDORELLI AG, EL HACHEM M, ZAMBRUNO G, et al. Notching up knowledge on molecular mechanisms of skin fibrosis: focus on the multifaceted Notch signalling pathway [J]. J Biomed Sci, 2021, 28(1): 36.
[3] AKIL A, GUTIERREZ-GARCIA AK, GUENTER R, et al. Notch signaling in vascular endothelial cells, angiogenesis, and tumor progression: an update and prospective [J]. Front Cell Dev Biol, 2021, 9: 642352.
[4] ZHOU B, LIN W, LONG Y, et al. Notch signaling pathway: architecture, disease, and therapeutics [J]. Signal Transduct Target Ther, 2022, 7(1): 95.
[5] FERREIRA A, ASTER JC. Notch signaling in cancer: complexity and challenges on the path to clinical translation [J]. Semin Cancer Biol, 2022, 85: 95-106.
[6] CANALIS E. Clinical and experimental aspects of notch receptor signaling: Hajdu-Cheney syndrome and related disorders [J]. Metabolism, 2018, 80: 48-56.
[7] TEODORCZYK M, SCHMIDT MHH. Notching on cancer's door: Notch signaling in brain tumors [J]. Front Oncol, 2014, 4: 341.
[8] AGGARWAL V, TULI HS, VAROL M, et al. NOTCH signaling: journey of an evolutionarily conserved pathway in driving tumor progression and its modulation as a therapeutic target [J]. Crit Rev Oncol Hematol, 2021, 164: 103403.
[9] BAZZONI R, BENTIVEGNA A. Role of Notch signaling pathway in glioblastoma pathogenesis [J]. Cancers (Basel), 2019, 11(3): 292.
[10] AYAZ F, OSBORNE BA. Non-canonical Notch signaling in cancer and immunity [J]. Front Oncol, 2014, 4: 345.
[11] SHABANI M, JAVANSHIR HT, BEREIMIPOUR A, et al. Contradictory effect of notch1 and notch2 on phosphatase and tensin homolog and its influence on glioblastoma angiogenesis [J]. Galen Med J, 2021, 10: e2091.
[12] LI Y, ZHOU XC, TAO L, et al. Notch1 signaling pathway promotes invasion, self-renewal and growth of glioma initiating cells via modulating chemokine system CXCL12/CXCR4 [J]. J Exp Clin Cancer Res, 2019, 38(1): 339.
[13] SHEN Y, CHEN H, ZHANG J, et al. Increased Notch signaling enhances radioresistance of malignant stromal cells induced by glioma stem/progenitor cells [J]. PLoS One, 2015, 10(11): e0142594.
[14] LIU J, WANG X, CHEN AT, et al. ZNF117 regulates glioblastoma stem cell differentiation towards oligodendroglial lineage [J]. Nat Commun, 2022, 13(1): 2196.
[15] LIANG W, GUO B, YE J, et al. Vasorin stimulates malignant progression and angiogenesis in glioma [J]. Cancer Sci, 2019, 110(8): 2558-2572.
[16] SENGUPTA S, MONDAL M, PRASASVI KR, et al. Differentiated glioma cell-derived fibromodulin activates integrin-dependent Notch signaling in endothelial cells to promote tumor angiogenesis and growth [J]. Elife, 2022, 11: e78972.
[17] JING X, YANG F, SHAO C, et al. Role of hypoxia in cancer therapy by regulating the tumor microenvironment [J]. Mol Cancer, 2019, 18 (1): 157.
[18] QIANG L, WU T, ZHANG HW, et al. HIF-1alpha is critical for hypoxia-mediated maintenance of glioblastoma stem cells by activating Notch signaling pathway [J]. Cell Death Differ, 2012, 19(2): 284-294.
[19] MAN J, YU X, HUANG H, et al. Hypoxic induction of vasorin regulates Notch1 turnover to maintain glioma stem-like cells [J]. Cell Stem Cell, 2018, 22(1): 104-18 e6.
[20] GAO K, JI Z, SHE K, et al. Long non-coding RNA ZFAS1 is an unfavourable prognostic factor and promotes glioma cell progression by activation of the Notch signaling pathway [J]. Biomed Pharmacother, 2017, 87: 555-560.
[21] MACIACZYK D, PICARD D, ZHAO L, et al. CBF1 is clinically prognostic and serves as a target to block cellular invasion and chemoresistance of EMT-like glioblastoma cells [J]. Br J Cancer, 2017, 117(1): 102-112.
[22] ALAFATE W, XU D, WU W, et al. Loss of PLK2 induces acquired resistance to temozolomide in GBM via activation of notch signaling [J]. J Exp Clin Cancer Res, 2020, 39(1): 239.
[23] HERRERA-RIOS D, LI G, KHAN D, et al. A computational guided, functional validation of a novel therapeutic antibody proposes Notch signaling as a clinical relevant and druggable target in glioma [J]. Sci Rep, 2020, 10(1): 16218.
[24] HAN QF, LI WJ, HU KS, et al. Exosome biogenesis: machinery, regulation, and therapeutic implications in cancer [J]. Mol Cancer, 2022, 21(1): 207.
[25] SUN Z, WANG L, ZHOU Y, et al. Glioblastoma stem cell-derived exosomes enhance stemness and tumorigenicity of glioma cells by transferring Notch1 protein [J]. Cell Mol Neurobiol, 2020, 40(5): 767-784.

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备注/Memo

备注/Memo:
(2023-03-20收稿,2023-11-06修回)
通信作者:李 舜,Email:morelee@163.com
更新日期/Last Update: 2024-11-30