scholarly journals Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer

Author(s):  
Kang Lin ◽  
Xiaojian Zhu ◽  
Chen Luo ◽  
Fanqin Bu ◽  
Jinfeng Zhu ◽  
...  
2009 ◽  
Vol 8 (8) ◽  
pp. 1878-1890 ◽  
Author(s):  
Yanlei Ma ◽  
Jiayuan Peng ◽  
Weijie Liu ◽  
Peng Zhang ◽  
Long Huang ◽  
...  

Oncotarget ◽  
2018 ◽  
Vol 9 (53) ◽  
pp. 30079-30091 ◽  
Author(s):  
Yu Yoshida ◽  
Takanori Goi ◽  
Hidetaka Kurebayashi ◽  
Mitsuhiro Morikawa ◽  
Yasuo Hirono ◽  
...  

2020 ◽  
Author(s):  
Linlin Xing ◽  
Mengyan Xia ◽  
Xin Jiao ◽  
Ling Fan

Abstract Background: Colorectal cancer (CRC) is a common malignant tumor with unsatisfactory overall prognosis. CircRNAs could be promising prognostic biomarkers in cancers, and play important role in the process of tumorigenesis and progression. Here, we explored the role of hsa_circ_0004831 in blood extracellular vesicles and its prognostic value in CRC. Methods: The circRNA and mRNA expression level matrix in extracellular vesicles of CRC and normal samples were obtained from the exoRBase database. The corresponding miRNA expression level matrix in extracellular vesicles was downloaded from the BBCancer database. Differentially expressed circRNAs, miRNAs and mRNAs were identified using the limma package of R software at the cut-off criteria of fold change (FC) > 2 and adj. p < 0.05. RT-qPCR assay was conducted to measure hsa_circ_0004831 expression level in CRC blood samples. A circRNA-miRNA-mRNA regulatory network of hsa_circ_0004831 was constructed based on competitive endogenous RNA mechanism and differentially expressed genes. The mRNAs co-expressed with hsa_circ_0004831 were screened at the cut-off criteria of pearson |r| > 0.3 and p < 0.05. Gene set enrichment analysis (GSEA) based on co-expressed mRNAs was used to explore the potential molecular function of hsa_circ_0004831. Results: Differentially expressed circRNAs, miRNAs and mRNAs were identified and hsa_circ_0004831 had a FC value of 3.92 in CRC blood extracellular vesicles. The RT-qPCR assay showed that the hsa_circ_0004831 was up-regulated in CRC blood samples. The overall survival analysis found that high expression of hsa_circ_0004831 was linked with poorer prognosis. Finally, a circRNA-miRNA-mRNA regulatory network of hsa_circ_0004831 was constructed based on down-regulated miR-4326 and 12 up-regulated mRNAs. GSEA indicated that mRNAs co-expressed with hsa_circ_0004831 were involved in EMT, WNT and p53 signaling pathways.Conclusions: The study confirmed the up-regulation of hsa_circ_0004831 in CRC, and it may act as a vital prognostic biomarker. The circRNA-miRNA-mRNA regulatory network of hsa_circ_0004831 could be used to uncover the tumorigenesis and progression of CRC.


2015 ◽  
Vol 2 (2) ◽  
pp. 82
Author(s):  
Monica Alvarado ◽  
Hilary Kershberg ◽  
George Tiller ◽  
Patty Miller ◽  
Ivan Lizarraga ◽  
...  

Oncotarget ◽  
2016 ◽  
Vol 7 (29) ◽  
pp. 46158-46172 ◽  
Author(s):  
Zhiliang Wei ◽  
Shougen Cao ◽  
Shanglong Liu ◽  
Zengwu Yao ◽  
Teng Sun ◽  
...  

2017 ◽  
Vol 49 (11) ◽  
pp. e391-e391 ◽  
Author(s):  
Hyun-Chul Kim ◽  
Junghwa Chang ◽  
Hannah S Lee ◽  
Ho Jeong Kwon

Author(s):  
Mitsuaki Nishioka ◽  
Yutaka Suehiro ◽  
Kouhei Sakai ◽  
Toshihiko Matsumoto ◽  
Naoko Okayama ◽  
...  

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