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下一代测序技术在食管鳞状细胞癌中早期生长反应-1 潜在调控基因和 microRNAs 的研究

Next Generation Sequencing for Potential Regulated Genes and Micro-RNAs of Early Growth Response-1 in the Esophageal Squamous Cell Carcinoma.

机构信息

Division of Thoracic Surgery, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

出版信息

Protein J. 2022 Dec;41(6):563-571. doi: 10.1007/s10930-022-10079-0. Epub 2022 Oct 7.

DOI:10.1007/s10930-022-10079-0
PMID:36207572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9668960/
Abstract

Esophageal cancer has a poor prognosis due to its aggressiveness and low survival rate. In Ease Asia, esophageal squamous cell carcinoma (ESCC) outnumbers esophageal adenocarcinoma (EAC). The ESCC patients still have high mortality despite modern surgical resection and neoadjuvant treatment. Determining patient and outcome prognostic factors is critical in ESCC treatment. In esophageal cancer, early growth response-1 (Egr-1) is a tumor suppressor gene, but the mechanism and associated genes are unknown. The study utilizes RNA interference method, the platform of Next Generation Sequencing (NGS) and bioinformatics analysis to investigate the influences after the Egr-1 gene slicing on the ESCC cells. The heat maps of differentially expressed mRNA and microRNAs were analyzed using the algorithm, Burrows-Wheller Aligner. The study showed that the expression of 51 mRNA and 26 microRNAs have significant changes in ESCC cells after Egr-1 knockdown. The KEGG enrichment analysis linked Egr-1-regulated genes and microRNAs. Egr-1 interactions with these genes and microRNAs may be important in tumor progression. In conclusions, this study provided the transcriptome patterns and relating pathway analysis for Egr-1 knockdown in ESCC cells. The mRNA and microRNAs altered by Egr-1 gene silencing might provide key information in the treatment of ESCC.

摘要

由于食管癌具有侵袭性和低生存率,因此预后较差。在东亚地区,食管鳞状细胞癌(ESCC)的发病率高于食管腺癌(EAC)。尽管采用了现代手术切除和新辅助治疗,ESCC 患者的死亡率仍然很高。确定患者和预后的相关因素对于 ESCC 的治疗至关重要。在食管癌中,早期生长反应因子-1(Egr-1)是一种肿瘤抑制基因,但具体机制和相关基因尚不清楚。本研究利用 RNA 干扰方法、下一代测序(NGS)平台和生物信息学分析,研究 Egr-1 基因切割对 ESCC 细胞的影响。使用 Burrows-Wheller Aligner 算法分析差异表达的 mRNA 和 microRNAs 的热图。研究表明,Egr-1 敲低后 ESCC 细胞中 51 个 mRNA 和 26 个 microRNA 的表达有明显变化。KEGG 富集分析将 Egr-1 调控的基因和 microRNAs 联系起来。Egr-1 与这些基因和 microRNAs 的相互作用可能在肿瘤进展中很重要。总之,本研究为 ESCC 细胞中 Egr-1 敲低提供了转录组图谱和相关通路分析。Egr-1 基因沉默改变的 mRNA 和 microRNAs 可能为 ESCC 的治疗提供关键信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/559daa18d8c9/10930_2022_10079_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/6813b730f4f5/10930_2022_10079_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/638d315a9729/10930_2022_10079_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/1adbcb036a79/10930_2022_10079_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/53c988997e20/10930_2022_10079_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/559daa18d8c9/10930_2022_10079_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/6813b730f4f5/10930_2022_10079_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/638d315a9729/10930_2022_10079_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/1adbcb036a79/10930_2022_10079_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/53c988997e20/10930_2022_10079_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3cd/9668960/559daa18d8c9/10930_2022_10079_Fig5_HTML.jpg

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