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鉴定参与聚(ADP-核糖)聚合酶-1(PARP-1)抑制剂耐药的新基因表达模式和途径。

Identification of novel gene expression patterns and pathways involved in PARP-1 inhibitor resistance.

作者信息

Khan Zulfa, Gomatam Anish, Murty Upadhyayula Suryanarayana, Dixit Vaibhav A

机构信息

Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research, (NIPER Guwahati), Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Govt. of India, Sila Katamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.

出版信息

Mamm Genome. 2025 May 22. doi: 10.1007/s00335-025-10134-y.

Abstract

US-FDA has approved PARP-1 inhibitors (Talazoparib, Olaparib, Rucaparib, and Niraparib) as the first line of treatment for many cancer types (e.g., breast, ovarian, pancreatic, and prostate) caused by mutations in breast cancer gene 1 and 2 (BRCA1/2). However, developing resistance to PARP-1 inhibitors is a major concern, which limits therapeutic effectiveness. In the present study, we identified novel gene signatures implicated in developing resistance to Olaparib. Meta-analysis was performed on publicly available RNA-Seq data related to ovarian and breast cancers from the GEO (Gene Expression Omnibus) database. Differential gene expression analysis, gene ontology, KEGG pathway enrichment, and protein-protein interaction (PPI) networking analyses were performed. A total of 139 Common DEGs (Differentially Expressed Genes) were identified, comprising 69 and 70 genes that were upregulated and downregulated respectively. KEGG Pathways "P53 signaling pathway" and "Positive regulation of developmental process(BP)", "endoplasmic reticulum lumen(CC)," and "growth factor binding(MF)", were found to be potentially associated with Olaparib resistance. Five hub genes were identified using PPI networking of which FN1, CCN2, and JUN may play a significant role in the development of Olaparib resistance and could be promising therapeutic and diagnostic biomarkers for dealing with Olaparib resistance in BRCA1/2 mutant breast and ovarian cancer.

摘要

美国食品药品监督管理局(US-FDA)已批准聚(ADP-核糖)聚合酶-1(PARP-1)抑制剂(他拉唑帕尼、奥拉帕尼、鲁卡帕尼和尼拉帕尼)作为由乳腺癌基因1和2(BRCA1/2)突变引起的多种癌症类型(如乳腺癌、卵巢癌、胰腺癌和前列腺癌)的一线治疗药物。然而,对PARP-1抑制剂产生耐药性是一个主要问题,这限制了治疗效果。在本研究中,我们确定了与奥拉帕尼耐药性发展相关的新基因特征。对来自基因表达综合数据库(GEO)的与卵巢癌和乳腺癌相关的公开可用RNA测序数据进行了荟萃分析。进行了差异基因表达分析、基因本体论、KEGG通路富集和蛋白质-蛋白质相互作用(PPI)网络分析。共鉴定出139个常见差异表达基因(DEGs),其中分别有69个和70个基因上调和下调。发现KEGG通路“P53信号通路”和“发育过程的正调控(BP)”、“内质网腔(CC)”以及“生长因子结合(MF)”可能与奥拉帕尼耐药性相关。使用PPI网络鉴定出5个枢纽基因,其中纤连蛋白1(FN1)、结缔组织生长因子(CCN2)和原癌基因c-Jun(JUN)可能在奥拉帕尼耐药性发展中起重要作用,并且可能成为应对BRCA1/2突变型乳腺癌和卵巢癌中奥拉帕尼耐药性的有前景的治疗和诊断生物标志物。

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