Analysis of Differential Expression of microRNAs and Their Target Genes in Prostate Cancer: A Bioinformatics Study on Microarray Gene Expression Data

被引:3
作者
Khorasani, Maryam [1 ]
Shahbazi, Shirin [2 ]
Hosseinkhan, Nazanin [3 ]
Mahdian, Reza [1 ]
机构
[1] Pasteur Inst Iran, Mol Med Dept, Tehran, Iran
[2] Tarbiat Modares Univ, Fac Med Sci, Dept Med Genet, Tehran, Iran
[3] Iran Univ Med Sci, Endocrine Res Ctr, Inst Endocrinol & Metab, Tehran, Iran
关键词
Prostate cancer; differential expression; microRNA; gene; biomarker; bioinformatics; IDENTIFICATION; TISSUE; RECURRENCE; BIOMARKERS; PATHWAYS; MEDICINE; MIRNA;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Early diagnosis of prostate cancer (PCa) as the second most common cancer in men is not associated with precise and specific results. Thus, alternate methods with high specificity and sensitivity are needed for accurate and timely detection of PCa. MicroRNAs regulate the molecular pathways involved in cancer by targeting multiple genes. The aberrant expression of the microRNAs has been reported in different cancer types including PCa. In this bioinfonnatics study, we studied differential expression profiles of microRNAs and their target genes in four PCa gene expression omnibus (GEO) databases. PCa diagnostic biomarker candidates were investigated using bioinformatics tools for analysis of gene expression data, microRNA target prediction, pathway and GO annotation, as well as ROC curves. The results of this study revealed significant changes in the expression of 14 microRNAs and 40 relevant target genes, which ultimately composed four combination panels (miR- 375+96+663/ miR- 133b+143- 3p + 205/ C2ORF72 + ENTPD5 + GLYAT11/LAAIB3 + NTVG2+TSLP) as candidate biomarkers capable to distinguish between PCa tumor samples and normal prostate tissue samples. These biomarkers may be suggested for a more accurate early diagnosis of PCa patients along with current diagnostic tests.
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页数:15
相关论文
共 45 条
[1]  
Alford Ashley V, 2017, Rev Urol, V19, P221, DOI 10.3909/riu0772
[2]  
[Anonymous], ONCOTARGET
[3]  
[Anonymous], CANCERS BASEL
[4]  
[Anonymous], RES CLIN APPL CANC S
[5]   Heatmapper: web-enabled heat mapping for all [J].
Babicki, Sasha ;
Arndt, David ;
Marcu, Ana ;
Liang, Yongjie ;
Grant, Jason R. ;
Maciejewski, Adam ;
Wishart, David S. .
NUCLEIC ACIDS RESEARCH, 2016, 44 (W1) :W147-W153
[6]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[7]   Identification of hub genes and potential molecular mechanisms in gastric cancer by integrated bioinformatics analysis [J].
Cao, Ling ;
Chen, Yan ;
Zhang, Miao ;
Xu, De-quan ;
Liu, Yan ;
Liu, Tonglin ;
Liu, Shi-xin ;
Wang, Ping .
PEERJ, 2018, 6
[8]   ROC-ing along: Evaluation and interpretation of receiver operating characteristic curves [J].
Carter, Jane V. ;
Pan, Jiamnin ;
Rai, Shesh N. ;
Galandiuk, Susan .
SURGERY, 2016, 159 (06) :1638-1645
[9]   Identification of protein biomarkers and signaling pathways associated with prostate cancer radioresistance using label-free LC-MS/MS proteomic approach [J].
Chang, Lei ;
Ni, Jie ;
Beretov, Julia ;
Wasinger, Valerie C. ;
Hao, Jingli ;
Bucci, Joseph ;
Malouf, David ;
Gillatt, David ;
Graham, Peter H. ;
Li, Yong .
SCIENTIFIC REPORTS, 2017, 7
[10]   miR-143 Interferes with ERK5 Signaling, and Abrogates Prostate Cancer Progression in Mice [J].
Clape, Cyrielle ;
Fritz, Vanessa ;
Henriquet, Corinne ;
Apparailly, Florence ;
Fernandez, Pedro Luis ;
Iborra, Francois ;
Avances, Christophe ;
Villalba, Martin ;
Culine, Stephane ;
Fajas, Lluis .
PLOS ONE, 2009, 4 (10)