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Lncrna–Mirna–Mrna Networks of Gastrointestinal Cancers Representing Common and Specific Lncrnas and Mrnas Publisher



Dastsooz H1, 2, 3 ; Alizadeh A4 ; Habibzadeh P5 ; Nariman A6 ; Hosseini A7 ; Mansoori Y8, 9 ; Haghiaminjan H10
Authors
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Authors Affiliations
  1. 1. Department of Life Sciences and Systems Biology, University of Turin, Turin, Italy
  2. 2. Candiolo, C/o IRCCS, IIGM-Italian Institute for Genomic Medicine, Turin, Italy
  3. 3. Candiolo Cancer (IT), FPO-IRCCS, Candiolo Cancer Institute, Turin, Italy
  4. 4. Medical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran
  5. 5. Research Center for Health Sciences, Institute of Health, Shiraz University of Medical Sciences, Shiraz, Iran
  6. 6. Genetics and Molecular Biology Department, Isfahan University of Medical Sciences, Isfahan, Iran
  7. 7. Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran
  8. 8. Department of Medical Genetics, Fasa University of Medical Sciences, Fasa, Iran
  9. 9. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran
  10. 10. Pharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran

Source: Frontiers in Genetics Published:2022


Abstract

Gastrointestinal (GI) cancers are responsible for approximately half of cancer-related deaths, highlighting the need for the identification of distinct and common features in their clinicopathological characteristics. Long ncRNA (lncRNAs), which are involved in competitive endogenous RNA (ceRNA) networks with critical roles in biological processes, constitute a substantial number of non-coding RNAs. Therefore, our study aimed to investigate the similarities and differences in the ceRNA networks of The Cancer Genome Atlas (TCGA)-GI cancers. We performed a comprehensive bioinformatics analysis of ceRNA networks for TCGA-GI cancers in terms of the deferential mRNA, lncRNA, and miRNA expression levels, ceRNA networks, overall survival analysis, correlation analysis, pathological cancer stages, and gene set enrichment analysis. Our study revealed several common and distinct mRNAs and lncRNAs with prognostic values in these networks. It was specifically noteworthy that MAGI2-AS3 lncRNA was found to be shared in almost all GI cancers. Moreover, the most common shared mRNAs between GI cancers were MEIS1, PPP1R3C, ADAMTSL3, RIPOR2, and MYLK. For each cancer ceRNA network, we found that the expression level of a number of lncRNAs and mRNAs was specific. Furthermore, our study provided compelling evidence that several genes, most notably KDELC1, can act as novel proto-oncogenes in cancers. This, in turn, can highlight their role as new prognostic and therapeutic targets. Moreover, we found cell cycle and extracellular matrix structural constituent as the top shared KEGG and molecular function, respectively, among GI cancers. Our study revealed several known lncRNAs and known and unknown mRNAs in GI cancers with diagnostic and prognostic values. Copyright © 2022 Dastsooz, Alizadeh, Habibzadeh, Nariman, Hosseini, Mansoori and Haghi-Aminjan.
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