scholarly journals Prognostic value of long non-coding RNA ZEB1-AS1 in Chinese cancer patients

Medicine ◽  
2019 ◽  
Vol 98 (17) ◽  
pp. e15251 ◽  
Author(s):  
Xi Zhou ◽  
Yang-Hua Fan ◽  
Yan Wang ◽  
Fu Wang ◽  
Yong Liu
Medicine ◽  
2018 ◽  
Vol 97 (49) ◽  
pp. e13548 ◽  
Author(s):  
Chao Ma ◽  
Xing-Guo Nie ◽  
Yan-Li Wang ◽  
Da-Peng Wu ◽  
Qiu-dong Liang

Tumor Biology ◽  
2015 ◽  
Vol 37 (1) ◽  
pp. 897-903 ◽  
Author(s):  
Yihua Wu ◽  
Wei Lu ◽  
Jinming Xu ◽  
Yu Shi ◽  
Honghe Zhang ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 9 (8) ◽  
pp. 8100-8110 ◽  
Author(s):  
Rui-Hua Liu ◽  
Ming-Ying Wang ◽  
Ling-Yun Chen ◽  
Zhi-Jie Yin ◽  
Qian-Kun Ji ◽  
...  

2021 ◽  
Vol 11 (3) ◽  
pp. 380-385
Author(s):  
Pengju Yue ◽  
Jing Bao

This study investigated the prognostic value of the long non-coding RNA (lncRNA) LINC01586 in pancreatic cancer. Three pancreatic cancer patients who received pancreaticoduodenectomies in our department in January 2019 were retrospectively selected. Cancer tissue and adjacent tissue samples were collected for high-throughput sequencing of lncRNAs. Among them, 221 lncRNAs were up-regulated and 235 were down-regulated. The expression of LINC01586 was decreased in pancreatic cancer patients (logFC = -3.308). An additional 74 tissue specimens were collected from pancreatic cancer patients from January 2011 to December 2016 for low-throughput validation. Patient samples were categorized into overexpression and low expression groups, based on the median LINC01586 expression level. The LINC01586 low expression group exhibited larger tumor size than the overexpression group (P < 0.001), while the low expression group exhibited a lower cancer-related survival rate than the overexpression group (one-year cancer-related survival rate: 55.6% vs. 89.2%, P < 0.001). Further analysis confirmed that low expression of LINC01586 was associated with poor prognosis for pancreatic cancer patients (OR = 0.169, 95% CI 0.066-0.437, P = 0.000). KEGG signaling pathway analysis was used to enrich LINC01586 target genes, and were mainly related to two metabolic pathways: insulin secretion (P = 0.011) and dopaminergic synapses (P = 0.0129), with SNAP25 as the core gene. The expression of LINC01586 and SNAP25were positively correlated in pancreatic cancer (R = 0.81 and P < 0.001). Together, our results indicate that LINC01586 may be used as a biomarker for prognosis predictions in pancreatic cancer patients, and its low expression is associated with poor prognosis.


Oncotarget ◽  
2017 ◽  
Vol 8 (54) ◽  
pp. 93227-93235 ◽  
Author(s):  
Liyang Liu ◽  
Jianfei Wen ◽  
Xi Gu ◽  
Dongdong Wu ◽  
Ming Lu ◽  
...  

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Yu Zhong ◽  
Liting Yang ◽  
Fang Xiong ◽  
Yi He ◽  
Yanyan Tang ◽  
...  

AbstractActin filament associated protein 1 antisense RNA 1 (named AFAP1-AS1) is a long non-coding RNA and overexpressed in many cancers. This study aimed to identify the role and mechanism of AFAP1-AS1 in lung cancer. The AFAP1-AS1 expression was firstly assessed in 187 paraffin-embedded lung cancer and 36 normal lung epithelial tissues by in situ hybridization. The migration and invasion abilities of AFAP1-AS1 were investigated in lung cancer cells. To uncover the molecular mechanism about AFAP1-AS1 function in lung cancer, we screened proteins that interact with AFAP1-AS1 by RNA pull down and the mass spectrometry analyses. AFAP1-AS1 was highly expressed in lung cancer clinical tissues and its expression was positively correlated with lung cancer patients’ poor prognosis. In vivo experiments confirmed that AFAP1-AS1 could promote lung cancer metastasis. AFAP1-AS1 promoted lung cancer cells migration and invasion through interacting with Smad nuclear interacting protein 1 (named SNIP1), which inhibited ubiquitination and degradation of c-Myc protein. Upregulation of c-Myc molecule in turn promoted the expression of ZEB1, ZEB2, and SNAIL gene, which ultimately enhanced epithelial to mesenchymal transition (EMT) and lung cancer metastasis. Understanding the molecular mechanism by which AFAP1-AS1 promotes lung cancer’s migration and invasion may provide novel therapeutic targets for lung cancer patients’ early diagnosis and therapy.


Head & Neck ◽  
2018 ◽  
Vol 40 (7) ◽  
pp. 1555-1564 ◽  
Author(s):  
Sulsal-Ul Haque ◽  
Liang Niu ◽  
Damaris Kuhnell ◽  
Jacob Hendershot ◽  
Jacek Biesiada ◽  
...  

2018 ◽  
Vol 484 ◽  
pp. 91-98 ◽  
Author(s):  
Chaojie Liang ◽  
Jing Liu ◽  
Hua Ge ◽  
Yingchen Xu ◽  
Guangming Li ◽  
...  

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