膀胱癌的基因图谱和通路分析:治疗靶向的意义。

IF 0.6 Q4 SURGERY
Sampara Vasishta, Usha Sachidananda Adiga, Alfred J Augustine
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引用次数: 0

摘要

目的:膀胱癌因其分子异质性而成为肿瘤学领域的一个重大挑战。本研究旨在明确膀胱癌发病机制的关键遗传因素和分子通路,促进膀胱癌靶向治疗的发展。材料与方法:从疾病基因网络数据库中检索膀胱癌的前30位相关基因。使用各种富集工具进行全面的生物信息学分析,包括基因本体生物学过程、细胞成分、分子功能分析,以及通过WikiPathways绘制途径图和通过人类代谢组数据库进行代谢物关联。使用DrugMatrix数据评估药物相互作用。结果:基因本体分析显示癌症相关的生物过程、细胞成分和分子功能显著富集。通路分析发现与头颈部鳞状细胞癌、癌症通路、胸膜间皮瘤、子宫内膜癌和膀胱癌通路有很强的相关性。关键基因包括CDKN2A、PTEN、EGFR、PIK3CA、HRAS、FGFR3和TP53,涉及多种途径。代谢物分析显示与磷脂酰肌醇衍生物显著相关,强调了PI3K途径的重要性。药物相互作用分析揭示了舍曲林、丙戊酸和羟基脲等化合物对膀胱癌基因表达模式的潜在调节作用。结论:该研究为膀胱癌的分子基础提供了全面的见解,突出了相互关联的途径和潜在的治疗靶点。与其他癌症类型的显著重叠提示可用于治疗干预的常见致癌机制。在临床样本中进一步验证这些发现可能有助于膀胱癌患者个性化治疗方法的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic profiling and pathway analysis in bladder carcinoma: Implications for therapeutic targeting.

Objective: Bladder carcinoma represents a significant challenge in oncology due to its heterogeneous molecular nature. This study aimed to identify key genetic factors and molecular pathways involved in bladder carcinoma pathogenesis to facilitate the development of targeted therapies.

Material and methods: The top 30 genes associated with bladder carcinoma were retrieved from the disease gene network database. Comprehensive bioinformatic analysis was performed using various enrichment tools, including gene ontology biological process, cellular component, molecular function analyses, and pathway mapping through WikiPathways and metabolite associations through human metabolome database. Drug interactions were evaluated using DrugMatrix data.

Results: Gene ontology analysis revealed significant enrichment of cancer-related biological processes, cellular components, and molecular functions. Pathway analysis identified strong associations with head and neck squamous cell carcinoma, cancer pathways, pleural mesothelioma, endometrial cancer, and bladder cancer pathways. Key genes including CDKN2A, PTEN, EGFR, PIK3CA, HRAS, FGFR3, and TP53 were implicated across multiple pathways. Metabolite analysis showed significant associations with phosphatidylinositol derivatives, highlighting the importance of the PI3K pathway. Drug interaction analysis revealed potential modulatory effects of several compounds including sertraline, valproic acid, and hydroxyurea on gene expression patterns in bladder carcinoma.

Conclusion: This study provides comprehensive insights into the molecular underpinnings of bladder carcinoma, highlighting interconnected pathways and potential therapeutic targets. The significant overlap with other cancer types suggests common oncogenic mechanisms that could be exploited for therapeutic intervention. Further validation of these findings in clinical samples may facilitate the development of personalized treatment approaches for bladder carcinoma patients.

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
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