探索羊膜母细胞瘤中神经营养素信号通路的基因网络和蛋白质相互作用分析。

In silico pharmacology Pub Date : 2024-06-10 eCollection Date: 2024-01-01 DOI:10.1007/s40203-024-00223-2
Sidhra Syed Zameer Ahmed, Manimaran Vetrivel, Syed Zameer Ahmed Khader, Yoithapprabhunath Thuckanaickenpalayam Ragunathan, SriChinthu Kenniyan Kumar, Puniethaa Prabhu, Dharani Lakshmi Devi Rajaram
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引用次数: 0

摘要

釉母细胞瘤是一种非癌症但具有侵袭性的口腔肿瘤,由牙本质上皮组织在牙体形成过程中产生。由于缺乏对釉母细胞瘤完整分子发病机制的揭示,化疗的尝试较少,对最佳治疗方案也存在很多分歧。因此,迄今为止,广泛手术切除被认为是治疗釉母细胞瘤的可靠方法。神经营养素信号通路在神经元信号传导中发挥着重要作用,它与 MAPK 通路密切相关,而 MAPK 通路则调控着细胞的分化、凋亡、增殖、可塑性和存活。利用 STRING 工具使用 WNL 值分析了蛋白质与蛋白质之间的相互作用,发现 CTNNB1、HRAS、NGFR、NGFR 和 SORT1 与 BDNF、NT4、p75NTR、NGF 和 NT3 有较高的相互作用。本体分析结果显示,神经营养素信号通路与细胞表面受体信号通路、细胞分化调控、发育过程调控、表皮生长因子受体酪氨酸激酶抑制剂抗性、MAPK 信号通路、PI3K-Akt 信号通路和 Ras 信号通路相关,导致涉及基因的发病。此外,BDNF、NT4、p75NTR、NGF 和 NT3 蛋白的聚类系数分别为 0.627、0.708、0.367、0.644 和 0.415。分子对接研究结果表明,在所选配体中,Methyl-ɣ-oresellinate、N-(4-羟基苯基)-2-苯基-N-苯乙酰基乙酰胺、Atranorin 和 Oresellinate 与所选蛋白质具有很高的结合亲和力。研究揭示了神经营养素信号通路中导致成釉细胞瘤发病机制的关键基因,这些基因与细胞分化、细胞增殖、促凋亡和促生存调控密切相关。由此可以得出结论,神经营养素信号通路可能是为治疗釉母细胞瘤定制靶向药物疗法的有前途的通路之一:在线版本包含补充材料,可查阅 10.1007/s40203-024-00223-2。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring gene network and protein interaction analysis of neurotrophin signaling pathway in ameloblastoma.

Ameloblastoma is a non-cancerous but aggressive oral tumor emerging from odontogenic epithelial tissue involved during odontogenesis. Since there is lack in unravelling the complete molecular pathogenesis of ameloblastoma, chemotherapy is less attempted and a lot of disagreement over the optimal treatment option. Hence, till date, wide surgical resection is considered to be the reliable treatment for ameloblastoma. The Neurotrophin Signaling pathway plays an important role in neuron signaling and it is closely related with the MAPK pathway, which on the other hand regulated cell differentiation, apoptosis, proliferation, plasticity and survival. Protein- Protein Interaction analysis was analysed with STRING tool using WNL value, identified that CTNNB1, HRAS, NGFR, NGFR, and SORT1 having high interacting with BDNF, NT4, p75NTR, NGF, and NT3. The results of ontology analysis revealed that Neurotrophin signaling pathway is associated with Cell surface receptor signaling pathway, regulation of cell differentiation, regulation of development process, EGFR tyrosine kinase inhibitor resistance, MAPK signaling pathway, PI3K-Akt signaling pathway and Ras signaling pathway leading to pathogenesis involving genes. Further, clustering coefficient values of proteins BDNF, NT4, p75NTR, NGF & NT3 were identified as 0.627, 0.708, 0.367, 0.644 & 0.415. The results of molecular docking studies revealed among the selected ligands Methyl-ɣ-oresellinate, N-(4-Hydroxy-phenyl)-2-phenyl-N-phenylacetyl-acetamide, Atranorin and Oresellinate exhibited high binding affinity with selected protein. The key genes involved in Neurotrophin signaling pathway leading to ameloblastoma pathogenesis is revealed, which are closely associated with cell differentiation, cell proliferation, pro-apoptosis, and pro-survival regulations. Further it can be concluded that Neurotrophin signaling pathway could be one of the promising pathway to tailor the targeted drug therapy for Ameloblastoma treatment.

Supplementary information: The online version contains supplementary material available at 10.1007/s40203-024-00223-2.

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