西妥昔单抗获得性耐药进展中的环状rna分析

IF 0.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Liping Yin, Changwen Jing, Yesong Guo
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引用次数: 0

摘要

我们采用高剂量脉冲法建立了西妥昔单抗耐药细胞系,并通过RNA测序寻找差异表达的环状RNA。数百个环状rna在敏感细胞和耐药细胞之间发生了改变。接下来,我们选择了六个显著差异的环状rna,并通过特定引物进行了定量实时PCR。京都基因和基因组百科全书通路分析显示,差异表达的环状rna在一些肿瘤相关通路中富集,如肿瘤转录调节、代谢、PI3K - Akt、mTOR等信号通路。我们的研究结果探索了与西妥昔单抗相关的差异表达环状rna,以寻找西妥昔单抗耐药治疗的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The analysis of the circRNAs in the progress of acquired resistance to Cetuximab
We established a Cetuximab‐resistant cell lines by high‐dose pulse method and searched for differentially expressed circular RNAs by RNA sequencing. Hundreds of circRNAs were altered between sensitive and resistant cells. Next, we chose six notably differential circRNAs and conducted quantitative real‐time PCR by specific primers. Kyoto Encyclopedia of Genes and Genomes pathway analysis revealed that differentially expressed circular RNAs are enriched in some tumor‐related pathways, such as tumor transcription regulation, metabolism, PI3K‐Akt, mTOR, and other signaling pathways. Our results explored differentially expressed circular RNAs associated with Cetuximab to find new targets for Cetuximab resistance therapy.
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来源期刊
Precision Medical Sciences
Precision Medical Sciences MEDICINE, RESEARCH & EXPERIMENTAL-
自引率
0.00%
发文量
33
审稿时长
15 weeks
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