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Gene expression profiling of lung adenocarcinoma in Xuanwei, China

机译:宣威市肺腺癌的基因表达谱

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摘要

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 11970 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.
机译:在中国宣威,肺癌的发病率和死亡率是世界上最高的。这项研究试图鉴定宣威地区与肺腺癌相关的差异表达基因(DEG)。通过微阵列获得八对配对的肺腺癌组织和相应的非肿瘤组织的表达谱。 DEG的功能注释通过生物信息学分析进行。通过实时定量PCR(RTq-PCR)进一步验证了微阵列的结果。宣威市肺腺癌中共有5290个基因被归类为DEGs。 3325个基因被上调,1965个基因被下调,而其他11970个基因的表达没有变化。这些DEG参与了许多与癌症有关的过程,包括细胞分裂,细胞粘附,细胞增殖和DNA复制,以及许多途径,例如p53信号途径,MAPK途径,Jak-STAT信号途径,刺猬信号通路和非小细胞肺癌通路。 RTq-中12个选定DEG(五个下调的基因,PIK3R1,RARB,HGF,MAPK11和SESN1)和七个上调的基因(PAK1,E2F1,CCNE1,EGF,CDC25A,PTTG1和UHRF1)的表达变化趋势PCR与表达谱数据一致。在低分化组中,PAK1的表达显着增加(P = 0.031),而在低分化组中,HGF的表达显着降低(P = 0.045)。非吸烟组的RARB和MAPK11显着增加(分别为P = 0.033和0.040)。宣威市肺腺癌中已检测到大量的DEGs,这可能使我们了解宣威市肺腺癌的发病机理,为防治宣威市肺腺癌奠定了重要基础。

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