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作 者:陈志贤 何凯 黄煜 曹琪 阮海龙 章小平 CHEN Zhixian;HE Kai;HUANG Yu;CAO Qi;RUAN Haihmg;ZHANG Xiaoping(Department of Urology,Union Hospital,Huazhong University of Science and Technology,Wuhan,430022,China)
机构地区:[1]华中科技大学同济医学院附属协和医院泌尿外科,武汉430022
出 处:《临床泌尿外科杂志》2021年第5期371-376,381,共7页Journal of Clinical Urology
基 金:国家自然科学基金(No:82002707)。
摘 要:目的:挖掘前列腺癌进展相关基因并探讨其在前列腺癌中的表达以及与临床参数之间的关系,预测其对前列腺癌进展和预后的影响。方法:通过Oncomine和GEO数据库筛选前列腺癌组织和癌旁组织的测序数据;运用R语言分析数据得到差异表达基因,取交集后筛选出前列腺素D2合成酶(PTGDS);分析其与前列腺癌临床参数以及与雄激素受体(AR)的相关性,通过基因富集分析(GSEA)研究PTGDS在肿瘤中可能的作用和功能。结果:PTGDS在前列腺癌组织中较正常组织呈现相对低表达;免疫组化进一步证实这种表达模式;PTGDS与多种临床参数相关,PTGDS低表达预示更差的预后;GSEA结果提示PTGDS与前列腺癌和AR密切相关,PTGDS表达水平与AR呈明显负相关。结论:PTGDS在前列腺癌中低表达,与前列腺癌的发生发展及多个临床参数相关,且与AR呈负相关,有潜力成为前列腺癌诊断和预后的新的生物标记物。Objective:To explore genes associated with the progression of prostate cancer and their relationships with clinical parameters,and to determine their values in predicting the prognosis of prostate cancer patients.Methods:Oncomine and GEO datasets were used to explore sequencing data about prostate cancer and adjacent normal tissue.R was performed to analyze the data and differentially expressed genes(DEGs)were obtained.We picked PTGDS out of the DEGs and analyzed its association with clinical parameters of prostate cancer and AR.GSEA was performed to reveal the possible roles of PTGDS in the development of prostate cancer.Results:PTGDS showed low expression in prostate cancer compared to normal tissue,which was further validated by immunohistochemical images.PTGDS was associated with many clinical parameters and low expression of PTGDS predicted poor prognosis.GSEA results indicated that PTGDS was closely related to prostate cancer and AR.Also,data from TCGA revealed a significantly negative correlation between PTGDS and AR in prostate cancer.Conclusion:PTGDS was down-regulated in prostate cancer and associated with the progression of prostate cancer and clinical parameters.It was also negatively correlated with AR expression level.It may become a new biomarker for diagnosis and predicting the prognosis of prostate cancer.
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