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Study on C/EBPα and FOXC2 expression in colon cancer lesions and preliminary analysis of their downstream target genes

机译:结肠癌病变中C /EBPα和FOXC2表达的研究及其下游靶基因的初步分析

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Objective: To study the C/EBPα and FOXC2 expression in colon cancer lesions and exploretheir downstream target genes. Methods: Colon cancer specimens surgically removed inWeinan Central Hospital between March 2014 and February 2017 were selected, and adjacenttissue specimens more than 5cm from tumor lesion margin were selected as control. TheRNA in the clinical specimens was extracted and the mRNA expression of C/EBPα, FOXC2as well as endoplasmic reticulum stress molecules and epithelial-mesenchymal transitionmolecules were determined. Results: C/EBPα, Bax, Bak, GRP78, PERK and ATF6 mRNAexpression levels in colon cancer specimens were significantly lower than those in adjacentsamples while FOXC2, FAK, SphK1, N-cadherin and Vimentin mRNA expression levels weresignificantly higher than those in adjacent specimens; Bax, Bak, GRP78, PERK and ATF6mRNA expression levels in colon cancer specimens with high C/EBPα expression weresignificantly higher than those in colon cancer specimens with low C/EBPα expression; FAK,SphK1, N-cadherin and Vimentin mRNA expression levels in colon cancer specimens withhigh FOXC2 expression were significantly higher than those in colon cancer specimens withlow FOXC2 expression. Conclusion: Lowly expressed C/EBPα and highly expressed FOXC2in colon cancer lesions can inhibit the apoptosis mediated by endoplasmic reticulum stress andpromote the cell invasion mediated by epithelial-mesenchymal transition.
机译:目的:研究结肠癌病灶中C /EBPα和FOXC2的表达,并探讨其下游靶基因。方法:选择2014年3月至2017年2月在渭南市中心医院外科手术切除的结肠癌标本,并选择距肿瘤病灶边缘5cm以上的癌旁组织作为对照。提取临床标本中的RNA,测定C /EBPα,FOXC2以及内质网应激分子和上皮间质转化分子的mRNA表达。结果:结肠癌标本中的C /EBPα,Bax,Bak,GRP78,PERK和ATF6 mRNA表达水平显着低于邻近样品,而FOXC2,FAK,SphK1,N-cadherin和Vimentin mRNA表达水平明显高于邻近标本。 ;具有高C /EBPα表达的结肠癌标本中的Bax,Bak,GRP78,PERK和ATF6mRNA表达水平明显高于具有低C /EBPα表达的结肠癌标本中的Bax,Bak,GRP78,PERK和ATF6mRNA表达水平。 FOXC2高表达的结肠癌标本中FAK,SphK1,N-cadherin和Vimentin mRNA的表达水平明显高于FOXC2低表达的结肠癌标本。结论:结肠癌病​​灶中低表达的C /EBPα和高表达的FOXC2可以抑制内质网应激介导的细胞凋亡,促进上皮-间质转化介导的细胞侵袭。

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