Initial study of microRNA expression profiles of colonic cancer without lymph node metastasis

2010 ◽  
Vol 11 (1) ◽  
pp. 50-54 ◽  
Author(s):  
Ying Xin WANG ◽  
Xiao Yan ZHANG ◽  
Bao Feng ZHANG ◽  
Chang Qing YANG ◽  
Xi Mei CHEN ◽  
...  
Oncogene ◽  
2003 ◽  
Vol 22 (14) ◽  
pp. 2192-2205 ◽  
Author(s):  
Takefumi Kikuchi ◽  
Yataro Daigo ◽  
Toyomasa Katagiri ◽  
Tatsuhiko Tsunoda ◽  
Koichi Okada ◽  
...  

2008 ◽  
Vol 51 (6) ◽  
pp. 891-896 ◽  
Author(s):  
Arne E. Faerden ◽  
Ole Sjo ◽  
Solveig Norheim Andersen ◽  
Beate Hauglann ◽  
Naimy Nazir ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Xi Wang ◽  
Guangyu Gao ◽  
Zhengrong Chen ◽  
Zhihao Chen ◽  
Mingxiao Han ◽  
...  

Abstract Background Because its metastasis to the lymph nodes are closely related to poor prognosis, miRNAs and mRNAs can serve as biomarkers for the diagnosis, prognosis, and therapy of colorectal cancer (CRC). This study aimed to identify novel gene signatures in the lymph node metastasis of CRC. Methods GSE56350, GSE70574, and GSE95109 datasets were downloaded from the Gene Expression Omnibus (GEO) database, while data from 569 colorectal cancer cases were also downloaded from The Cancer Genome Atlas (TCGA) database. Differentially expressed miRNAs (DE-miRNAs) were calculated using R programming language (Version 3.6.3), while gene ontology and enrichment analysis of target mRNAs were performed using FunRich (http://www.funrich.org). Furthermore, the mRNA–miRNA network was constructed using Cytoscape software (Version 3.8.0). Gene expression levels were verified using the GEO datasets. Similarly, quantitative real-time PCR (qPCR) was used to examine expression profiles from 20 paired non-metastatic and metastatic lymph node tissue samples obtained from patients with CRC. Results In total, five DE-miRNAs were selected, and 34 mRNAs were identified after filtering the results. Moreover, two key miRNAs (hsa-miR-99a, hsa-miR-100) and one gene (heparan sulfate-glucosamine 3-sulfotransferase 2 [HS3ST2]) were identified. The GEO datasets analysis and qPCR results showed that the expression of key miRNA and genes were consistent with that obtained from the bioinformatic analysis. A novel miRNA–mRNA network capable of predicting the prognosis and confirmed experimentally, hsa-miR-99a-HS3ST2-hsa-miR-100, was found after expression analysis in metastasized lymph node tissue from CRC samples. Conclusion In summary, miRNAs and genes with potential as biomarkers were found and a novel miRNA–mRNA network was established for CRC lymph node metastasis by systematic bioinformatic analysis and experimental validation. This network may be used as a potential biomarker in the development of lymph node metastatic CRC.


2004 ◽  
Vol 122 (1) ◽  
pp. 61-69 ◽  
Author(s):  
Minoru Takada ◽  
Mitsuhiro Tada ◽  
Eiji Tamoto ◽  
Akiko Kawakami ◽  
Katsuhiko Murakawa ◽  
...  

2012 ◽  
Vol 23 ◽  
pp. ix209
Author(s):  
M. Rammer ◽  
H. Rumpold ◽  
H. Bösmüller ◽  
R. Marschon ◽  
T. Malli ◽  
...  

2008 ◽  
Vol 51 (6) ◽  
pp. 987
Author(s):  
Arne E. Faerden ◽  
Ole H. Sjo ◽  
Solveig Norheim Andersen ◽  
Beate Hauglann ◽  
Naimy Nazir ◽  
...  

2011 ◽  
Vol 96 (3) ◽  
pp. 207-216 ◽  
Author(s):  
Toshiaki Watanabe ◽  
Takashi Kobunai ◽  
Yoko Yamamoto ◽  
Keiji Matsuda ◽  
Soichiro Ishihara ◽  
...  

Abstract In stage III colorectal cancer, patients with N1 stage tumors show poorer outcome than patients with N2 stage tumors. Our objective was to identify genes that are predictive for the presence of lymph node metastasis, and to characterize the aggressiveness of lymph node metastases. Gene expression profiles of colorectal cancer were determined by microarray in training (n  =  116) and test (n  =  25) sets of patients. We identified 40 discriminating probes in patients with and without lymph node metastases. Using these probes, we could predict the presence of lymph node metastasis with an accuracy of 87.1% (training set) and 76.0% (test set). Among discriminating probes, FOXC2 expression was significantly correlated with the degree of lymph node metastasis. FOXC2 was expressed significantly and disparately in patients with N1 and N2 stage tumors as analyzed by real-time reverse transcriptase–polymerase chain reaction. FOXC2 appears to be involved in determining the aggressiveness of lymph node metastasis in colorectal cancer.


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