Analysis of differentially expressed genes in oral epithelial cells infected with Fusobacterium nucleatum for revealing genes associated with oral cancer.

Analysis of differentially expressed genes in oral epithelial cells infected with Fusobacterium nucleatum for revealing genes associated with oral cancer.
复制标题

分析感染具核梭杆菌的口腔上皮细胞差异表达基因,揭示与口腔癌相关的基因

DOI:
10.1111/jcmm.16142
复制
发表时间:
2021-01
影响因子:
5.3
通讯作者:
Pan Y
Pan Y
中科院分区:
医学2区
文献类型:
--
作者:
Zhang S;Li C;Zhang Z;Li Y;Li Q;Geng F;Liu J;Pan Y

文献摘要

参考文献

被引文献

相似文献

Accumulating evidence links Fusobacterium nucleatum with tumorigenesis. Our previous study demonstrated that F. nucleatum infection can induce epithelial‐mesenchymal transition (EMT) in oral epithelial cells and elaborated a probable signal pathway involved in the induction of EMT. However, the comprehensive profiling and pathways of other candidate genes involved in F. nucleatum promoting malignant transformation remain largely elusive. Here, we analysed the transcriptome profile of HIOECs exposed to F. nucleatum infection. Totally, 3307 mRNAs (ǀLog2FCǀ >1.5) and 522 lncRNAs (ǀLog2FCǀ >1) were identified to be differentially expressed in F. nucleatum‐infected HIOECs compared with non‐infected HIOECs. GO and KEGG pathway analyses were performed to investigate the potential functions of the dysregulated genes. Tumour‐associated genes were integrated, and top 10 hub genes (FYN, RAF1, ATM, FOS, CREB, NCOA3, VEGFA, JAK2, CREM and ATF3) were identified by protein‐protein interaction (PPI) network, and Oncomine was used to validate hub genes' expression. LncRNA‐hub genes co‐expression network comprising 67 dysregulated lncRNAs were generated. Together, our study revealed the alteration of lncRNA and potential hub genes in oral epithelial cells in response to F. nucleatum infection, which may provide new insights into the shift of normal to malignant transformation initiated by oral bacterial infection.
DOI: 10.1016/j.mib.2014.11.013
发表时间: 2015-02
影响因子: 5.4
作者:
Han YW
通讯作者: Han YW
DOI: 10.3727/096504018x15228909735079
发表时间: 2019-02-21
期刊: Oncology research
影响因子: 3.1
作者:
Gao Y;Xu Y;Wang J;Yang X;Wen L;Feng J
通讯作者: Feng J
DOI: 10.1111/jcmm.14829
发表时间: 2019-12-19
影响因子: 5.3
作者:
Du, Xiaoliu;Tu, Yiming;Ji, Jing
通讯作者: Ji, Jing
CCL21/CCR7 相互作用通过 JAK2/STAT3 信号通路促进 EMT 并增强 OSCC 的干性
DOI: 10.1002/jcp.29525
发表时间: 2020-02-04
影响因子: 5.6
作者:
Chen, Yang;Shao, Zhe;Shang, Zhengjun
通讯作者: Shang, Zhengjun
DOI: 10.1002/jcb.29530
发表时间: 2019-11-06
影响因子: 4
作者:
Diao, Lei;Li, Yang;Hu, Jing
通讯作者: Hu, Jing