کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8457984 | 1548864 | 2018 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Upregulation of LncRNA FEZF-AS1 is associated with advanced clinical stages and family history of cancer in patients with NSCLC
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
تحقیقات سرطان
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چکیده انگلیسی
Antisense RNA (AS) is a type of long non-coding RNAs that functions as a post-transcriptional regulatory element on regulating parental coding gene expression via directly binding to complementary mRNA sequences. We aimed to investigate the effect of the AS to FEZF1 gene on non-small cell lung cancer (NSCLC) development. The expression level of lncRNA FEZF-AS1 and FEZF1 was determined by the quantitative Real-time PCR in 160 cases of NSCLC tissues and their adjacent non-tumour tissues. We found that lncRNA FEZF-AS1 was significantly up-regulated in tumour tissues when compared to the adjacent non-cancerous tissues (Pâ¯=â¯0.001), and it's high expression correlated with advanced stages (Pâ¯=â¯0.002) and Tumour Family History (Pâ¯=â¯0.029). Meanwhile, In 58 cases of NSCLC tissues the expression of lncRNA FEZF-AS1 was positively associated with that of FEZF1expression (râ¯=â¯0.8810, pâ¯=â¯1.6575E-20). By GEPIA database analysis, we also found that the expression of lncRNA FEZF-AS1 and FEZF1 were significantly higher in tumour tissues than those of the adjacent non-cancerous tissues in 969 NSCLC patients (Pâ¯<â¯0.05), and lncRNA FEZF-AS1 was positively correlated with FEZF1 (râ¯=â¯0.90, Pâ¯<â¯0.001). These results suggest that lncRNA FEZF-AS1 relate to the progression of lung cancer patients and it may be a potential target for cancer therapy.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Pathology - Research and Practice - Volume 214, Issue 6, June 2018, Pages 857-861
Journal: Pathology - Research and Practice - Volume 214, Issue 6, June 2018, Pages 857-861
نویسندگان
Wei Gong, Yi Cao, Yuanyuan Wang, Lei Yang, Wenpeng Su, Fuman Qiu, Soham Datta, Boqi Rao, Jianfeng Xian, Mingzhu Lin, Yingyi Feng, Xin Zhang, Yifeng Zhou, Xingcheng Gao, Jiachun Lu,