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首页> 外文期刊>Clinical and Translational Medicine >Comprehensive analysis of oncogenic signatures and consequent repurposed drugs in TMPRSS2:ERG fusion‐positive prostate cancer
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Comprehensive analysis of oncogenic signatures and consequent repurposed drugs in TMPRSS2:ERG fusion‐positive prostate cancer

机译:<斜视> TMPRSS2中的致癌签名综合分析及其重新灌注的药物:ERG 融合阳性前列腺癌

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TMPRSS2:ERG(TE)fusionoccursinapproximately50% ofallprostatecancercases. 1 However,detailsaboutaltered signaling or the difference of gene expression regarding potential therapeutic targets between TE fusion-positive and negative group is yet to be fully investigated. In this study, we investigated the landscape of molecular signal- ing and curated potential therapeutic targets in TE fusion- positive prostate cancers using The Cancer Genome Atlas data. Firstly, we identified 3870 genes in coordination with ERG in RNA expression and nine cancer-related pathways specifically altered in TE fusion-positive prostate cancer patients.Secondly,wededucedrepositionable55drugstar- getingforTEfusion-positiveprostatecancerfromnetwork analysis. Finally, we provided experimental data for six drugsobtainedfromourinsilicoanalysisandshowedsen- sitivity specific for TE fusion-positive prostate cancer cell line.
机译:TMPRSS2:ERG(TE)Fusionoccursinapply50%的AllProstatecancerces。 然而,详细说明了关于TE融合阳性和阴性组之间的潜在治疗靶标的基因表达的信令或基因表达的差异。 在这项研究中,我们研究了使用癌症基因组地图集数据的TE融合阳性前列腺癌中分子信号和愈合潜在治疗靶标的景观。 首先,我们鉴定了3870个与RNA表达中的ERG协调的基因,并在TE融合阳性前列腺癌患者中明确改变了九种癌症相关途径。第二个,WedeductionRepositable55Dugstar-Getfortefusion-PlactProstatecancerfromnetwork分析。 最后,我们提供了六种药物过量的实验数据,用于特异于TE融合阳性前列腺癌细胞的Showedsen-Sit度。

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