RFCM3: Computational Method for Identification of miRNA-mRNA Regulatory Modules in Cervical Cancer

Cervical cancer is a leading severe malignancy throughout the world. Molecular processes and biomarkers leading to tumor progression in cervical cancer are either unknown or only partially understood. An increasing number of studies have shown that microRNAs play an important role in tumorigenesis so understanding the regulatory mechanism of miRNAs in gene-regulatory network will help elucidate the complex biological processes that occur during malignancy. Functional genomics data provides opportunities to study the aberrant microRNA-messenger RNA (miRNA-mRNA) interaction. Identification of miRNA-mRNA regulatory modules will aid deciphering aberrant transcriptional regulatory network in cervical cancer but is computationally challenging. In this regard, an algorithm, termed as relevant and functionally consistent miRNA-mRNA modules (RFCM3), is proposed. It integrates miRNA and mRNA expression data of cervical cancer for identification of potential miRNA-mRNA modules. It selects set of miRNA-mRNA modules by maximizing relation of mRNAs with miRNA and functional similarity between selected mRNAs. Later, using the knowledge of the miRNA-miRNA synergistic network different modules are fused and finally a set of modules are generated containing several miRNAs as well as mRNAs. This type of module explains the underlying biological pathways containing multiple miRNAs and mRNAs. The effectiveness of the proposed approach over other existing methods has been demonstrated on a miRNA and mRNA expression data of cervical cancer with respect to enrichment analyses and other standard metrices. The prognostic value of the genes in a module with respect to cervical cancer is also demonstrated. The approach was found to generate more robust, integrated, and functionally enriched miRNA-mRNA modules in cervical cancer.

[1]  C. Burge,et al.  Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA Targets , 2005, Cell.

[2]  P. Shannon,et al.  Cytoscape: a software environment for integrated models of biomolecular interaction networks. , 2003, Genome research.

[3]  Scott B. Dewell,et al.  Transcriptome-wide Identification of RNA-Binding Protein and MicroRNA Target Sites by PAR-CLIP , 2010, Cell.

[4]  Martin Reczko,et al.  DIANA miRPath v.2.0: investigating the combinatorial effect of microRNAs in pathways , 2012, Nucleic Acids Res..

[5]  Pradipta Maji,et al.  $f$-Information Measures for Efficient Selection of Discriminative Genes From Microarray Data , 2009, IEEE Transactions on Biomedical Engineering.

[6]  Michael E. Davis,et al.  RESEARCH Integrative Cardiovascular Physiology and Pathophysiology High-throughput screening identifies microRNAs that target Nox2 and improve function after acute myocardial infarction , 2022 .

[7]  Michael Kertesz,et al.  The role of site accessibility in microRNA target recognition , 2007, Nature Genetics.

[8]  A. Martínez-Torteya,et al.  SurvExpress: An Online Biomarker Validation Tool and Database for Cancer Gene Expression Data Using Survival Analysis , 2013, PloS one.

[9]  Beverly L. Davidson,et al.  Elucidation of transcriptome-wide microRNA binding sites in human cardiac tissues by Ago2 HITS-CLIP , 2016, Nucleic acids research.

[10]  Jörg Vogel,et al.  Experimental approaches to identify non-coding RNAs , 2006, Nucleic acids research.

[11]  Weijun Luo,et al.  Pathview: an R/Bioconductor package for pathway-based data integration and visualization , 2013, Bioinform..

[12]  V. Ambros The functions of animal microRNAs , 2004, Nature.

[13]  Joshua M. Korn,et al.  Comprehensive genomic characterization defines human glioblastoma genes and core pathways , 2008, Nature.

[14]  G. Ruvkun,et al.  Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans , 1993, Cell.

[15]  Ming Lu,et al.  TransmiR: a transcription factor–microRNA regulation database , 2009, Nucleic Acids Res..

[16]  Steve Horvath,et al.  WGCNA: an R package for weighted correlation network analysis , 2008, BMC Bioinformatics.

[17]  V. Ambros,et al.  The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14 , 1993, Cell.

[18]  Benjamin J. Raphael,et al.  Integrated Genomic Analyses of Ovarian Carcinoma , 2011, Nature.

[19]  T. Wu,et al.  Focus on endometrial and cervical cancer. , 2004, Cancer cell.

[20]  Xinxia Peng,et al.  Computational identification of hepatitis C virus associated microRNA-mRNA regulatory modules in human livers , 2009, BMC Genomics.

[21]  Juan Liu,et al.  A novel computational framework for simultaneous integration of multiple types of genomic data to identify microRNA-gene regulatory modules , 2011, Bioinform..

[22]  Aedín C. Culhane,et al.  Public data and open source tools for multi-assay genomic investigation of disease , 2015, Briefings Bioinform..

[23]  Ben Lehner,et al.  Tissue specificity and the human protein interaction network , 2009, Molecular systems biology.

[24]  C. Burge,et al.  Most mammalian mRNAs are conserved targets of microRNAs. , 2008, Genome research.

[25]  R. Plasterk,et al.  The diverse functions of microRNAs in animal development and disease. , 2006, Developmental cell.

[26]  Cheng Liang,et al.  Mirsynergy: detecting synergistic miRNA regulatory modules by overlapping neighbourhood expansion , 2014, Bioinform..

[27]  Uwe Ohler,et al.  Viral microRNA targetome of KSHV-infected primary effusion lymphoma cell lines. , 2011, Cell host & microbe.

[28]  Davide Heller,et al.  STRING v10: protein–protein interaction networks, integrated over the tree of life , 2014, Nucleic Acids Res..

[29]  X. Wang,et al.  Let-7g targets collagen type I alpha2 and inhibits cell migration in hepatocellular carcinoma. , 2010, Journal of hepatology.

[30]  D. Bartel MicroRNAs: Target Recognition and Regulatory Functions , 2009, Cell.

[31]  S. Grover,et al.  Cervical cancer control in HIV-infected women: Past, present and future , 2017, Gynecologic oncology reports.

[32]  Igor Pogribny,et al.  Small molecules with big effects: the role of the microRNAome in cancer and carcinogenesis. , 2011, Mutation research.

[33]  Gabriele Sales,et al.  MAGIA, a web-based tool for miRNA and Genes Integrated Analysis , 2010, Nucleic Acids Res..

[34]  A. Zekri,et al.  miR-34a: Multiple Opposing Targets and One Destiny in Hepatocellular Carcinoma , 2016, Journal of clinical and translational hepatology.

[35]  Pradipta Maji,et al.  Rough Sets for Selection of Molecular Descriptors to Predict Biological Activity of Molecules , 2010, IEEE Transactions on Systems, Man, and Cybernetics, Part C (Applications and Reviews).

[36]  K. Gunsalus,et al.  Combinatorial microRNA target predictions , 2005, Nature Genetics.

[37]  O. Kent,et al.  A small piece in the cancer puzzle: microRNAs as tumor suppressors and oncogenes , 2006, Oncogene.

[38]  Brad T. Sherman,et al.  Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists , 2008, Nucleic acids research.

[39]  Anton J. Enright,et al.  Annotation of mammalian primary microRNAs , 2008, BMC Genomics.

[40]  Hyunju Lee,et al.  A Computational Approach to Identifying Gene-microRNA Modules in Cancer , 2015, PLoS Comput. Biol..

[41]  Dong Wang,et al.  Inferring the human microRNA functional similarity and functional network based on microRNA-associated diseases , 2010, Bioinform..

[42]  Xin Chen,et al.  TRANSFAC: an integrated system for gene expression regulation , 2000, Nucleic Acids Res..

[43]  D. Tollervey,et al.  Mapping the Human miRNA Interactome by CLASH Reveals Frequent Noncanonical Binding , 2013, Cell.

[44]  D. Kallmes,et al.  RNA-Sequencing Analysis of Messenger RNA/MicroRNA in a Rabbit Aneurysm Model Identifies Pathways and Genes of Interest , 2015, American Journal of Neuroradiology.

[45]  Kara Dolinski,et al.  The BioGRID Interaction Database: 2011 update , 2010, Nucleic Acids Res..

[46]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.

[47]  B. Cullen,et al.  In-Depth Analysis of the Interaction of HIV-1 with Cellular microRNA Biogenesis and Effector Mechanisms , 2013, mBio.

[48]  Sebastian D. Mackowiak,et al.  Circular RNAs are a large class of animal RNAs with regulatory potency , 2013, Nature.