Suppr超能文献

中国宣威肺腺癌的基因表达谱分析。

Gene expression profiling of lung adenocarcinoma in Xuanwei, China.

作者信息

Wu Huifei, Meng Shuangshuang, Xu Qiuyue, Wang Xiao, Wang Juan, Gong Rong, Song Yu, Duan Yong, Zhang Yanliang

机构信息

aDepartment of Clinical Laboratory, the First Affiliated Hospital of Kunming Medical University bYunnan Institute of Experimental Diagnosis, Kunming, People's Republic of China.

出版信息

Eur J Cancer Prev. 2016 Nov;25(6):508-17. doi: 10.1097/CEJ.0000000000000214.

Abstract

The morbidity and mortality of lung cancer in Xuanwei, China, are the highest in the world. This study attempts to identify differentially expressed genes (DEGs) related to lung adenocarcinoma in Xuanwei. The expression profiles of eight paired lung adenocarcinoma tissues and corresponding nontumor tissues were acquired by microarrays. Functional annotations of DEGs were carried out by bioinformatics analysis. The results of the microarrays were further verified by real-time quantitative PCR (RTq-PCR). A total of 5290 genes were classified as DEGs in lung adenocarcinoma in Xuanwei; 3325 genes were upregulated and 1965 genes were downregulated, whereas the expression of the other 11 970 genes did not change. These DEGs are involved in a wide range of cancer-related processes, which include cell division, cell adhesion, cell proliferation, and DNA replication, and in many pathways such as the p53 signaling pathway, the MAPK pathway, the Jak-STAT signaling pathway, the hedgehog signaling pathway, and the non-small-cell lung cancer pathway. The tendency of changes in the expression of 12 selected DEGs (five downregulated genes, PIK3R1, RARB, HGF, MAPK11, and SESN1, and seven upregulated genes, PAK1, E2F1, CCNE1, EGF, CDC25A, PTTG1, and UHRF1) in RTq-PCR was consistent with the expression profiling data. Expression of PAK1 was significantly increased in the low differentiation group (P=0.031), whereas expression of HGF was significantly decreased in the low differentiation group (P=0.045). RARB and MAPK11 were significantly increased in the nonsmoker group (P=0.033 and 0.040, respectively). A large number of DEGs in lung adenocarcinoma in Xuanwei have been detected, which may enable us to understand the pathogenesis and lay an important foundation for the prevention and treatment of lung adenocarcinoma in Xuanwei.

摘要

中国宣威肺癌的发病率和死亡率位居世界之首。本研究旨在鉴定与宣威肺腺癌相关的差异表达基因(DEG)。通过微阵列获取了8对肺腺癌组织及相应非肿瘤组织的表达谱。通过生物信息学分析对DEG进行功能注释。微阵列结果通过实时定量PCR(RTq-PCR)进一步验证。宣威肺腺癌中共有5290个基因被归类为DEG;3325个基因上调,1965个基因下调,而其他11970个基因的表达未发生变化。这些DEG参与了广泛的癌症相关过程,包括细胞分裂、细胞黏附、细胞增殖和DNA复制,以及许多信号通路,如p53信号通路、MAPK通路、Jak-STAT信号通路、刺猬信号通路和非小细胞肺癌通路。RTq-PCR中12个选定DEG(5个下调基因,PIK3R1、RARB、HGF、MAPK11和SESN1,以及7个上调基因,PAK1、E2F1、CCNE1、EGF、CDC25A、PTTG1和UHRF1)的表达变化趋势与表达谱数据一致。PAK1在低分化组中的表达显著增加(P = 0.031),而HGF在低分化组中的表达显著降低(P = 0.045)。RARB和MAPK11在非吸烟组中显著增加(分别为P = 0.033和0.040)。已检测到宣威肺腺癌中的大量DEG,这可能有助于我们了解其发病机制,并为宣威肺腺癌的防治奠定重要基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验