Differential expression of genes in HepG2 cells caused by UC001kfo RNAi as shown by RNA-seq
Differential expression of genes in HepG2 cells caused by UC001kfo RNAi as shown by RNA-seq
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RNA-seq显示UC001kfo RNAi引起的HepG2细胞中基因的差异表达
DOI:
10.1007/s11596-017-1765-1
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发表时间:
2017-08
期刊:
影响因子:
--
通讯作者:
Pan YF
中科院分区:
文献类型:
--
作者:
Pan YF
The differential expression of genes in HepG2 cells caused by UC001kfo RNAi was investigated using RNA-seq. HepG2 cells were infected by Lenti-shUC001kfo lentivirus particles. The expression of UC001kfo mRNA in the HepG2-shUC001kfo cell line was detected by real-time PCR. RNA-seq technology was used to identify the difference in the expression of genes regulated by lncRNA UC001kfo in the HepG2 cell line. Gene ontology and signaling pathway analysis were performed to reveal the biological functions of the genes encoding of significantly different mRNAs. The results showed that mRNAs were differentially expressed between the HepG2-shUC001kfo cell line and the HepG2 cell line. The UC001kfo mRNA was significantly down-regulated in the stable cell line HepG2-shUC001kfo (P<0.001). Additionally, we found 19 signaling pathways or functional classifications encompassing 30 genes that played a role in cancer characteristics, cell adhesion, invasion and migration. The results also showed that the expression of many genes associated with cancer cell invasion and metastasis was decreased with the down-regulation of the lncRNA UC001kfo. LncRNA UC001kfo may play a role in regulating cancer cell invasion and metastasis. It was suggested that mRNAs were differentially expressed in the HepG2 cell line after the down-regulation of lncRNA-UC001kfo. Some took part in the extracellular matrix, cell adhesion, motility, growth, and localization. The genes encoding of differentially expressed mRNAs may participate in cell invasion and metastasis.
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影响因子:
14.9
作者:
Kanehisa M;Araki M;Goto S;Hattori M;Hirakawa M;Itoh M;Katayama T;Kawashima S;Okuda S;Tokimatsu T;Yamanishi Y
通讯作者:
Yamanishi Y
影响因子:
5.3
作者:
Pradhan, Madhumita;Baumgarten, Sarah C.;Frasor, Jonna
通讯作者:
Frasor, Jonna
影响因子:
2.7
作者:
Wharton, KA;Zimmermann, G;Scott, MP
通讯作者:
Scott, MP
DOI:
10.1186/1756-9966-30-75
发表时间:
2011-08-12
期刊:
Journal of experimental & clinical cancer research : CR
影响因子:
--
作者:
Wong AW;Paulson QX;Hong J;Stubbins RE;Poh K;Schrader E;Nunez NP
通讯作者:
Nunez NP
影响因子:
5.2
作者:
Masaru Katoh
通讯作者:
Masaru Katoh