Abstract

Glioma is a lethal malignant brain cancer, and many reports have shown that abnormalities in the behavior of water and ion channels play an important role in regulating tumor proliferation, migration, apoptosis, and differentiation. Recently, new studies have suggested that some long noncoding RNAs containing small open reading frames can encode small peptides and form oligomers for water or ion regulation. However, because the peptides are difficult to identify, their functional mechanisms are far from being clearly understood. In this study, we used bioinformatics methods to identify and evaluate lncRNAs, which may encode small transmembrane peptides in gliomas. Combining ab initio homology modeling, molecular dynamics simulations, and free energy calculations, we constructed a predictive model and predicted the oligomer channel activity of peptides by identifying the lncRNA ORFs. We found that one key hub lncRNA, namely, DLEU1, which contains two smORFs (ORF1 and ORF8), encodes small peptides that form pentameric channels. The mechanics of water and ion (Na+ and Cl-) transport through this pentameric channel were simulated. The potential mean force of the H2O molecules along the two ORF-encoded peptide channels indicated that the energy barrier was different between ORF1 and ORF8. The ORF1-encoded peptide pentamer acted as a self-assembled water channel but not as an ion channel, and the ORF8 permeated neither ions nor water. This work provides new methods and theoretical support for further elucidation of the function of lncRNA-encoded small peptides and their role in cancer. Additionally, this study provides a theoretical basis for drug development.

Highlights

  • Glioma is one of the most prevalent types of primary intracranial carcinomas

  • A model was built from a glioma ceRNA network to screen for differentially expressed hub long noncoding RNAs (lncRNAs) and to identify open reading frames (ORFs) fragments encoding small TM peptides by bioinformatics methods and ab initio homology modeling combined with Molecular dynamics (MD) simulation

  • Our established models revealed that the small peptides of the two encodable ORFs (ORF1 and ORF8) of the DLEU1 lncRNA could form pentameric channels

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Summary

Introduction

Glioma is one of the most prevalent types of primary intracranial carcinomas. Glioma has varying malignancy grades and histological subtypes [1], and it remains a highly lethal. Small peptide prediction and channel function malignancy worldwide. Glioma is characterized by rapid cell proliferation and angiogenesis [2]. Traditional treatments have limited effectiveness in the majority of gliomas because glioblastoma (GBM) stem-like cells (GSCs) are highly recrudescent [3]. Investigations exploring the accurate molecular mechanisms of and reliable therapeutic targets for gliomas have attracted extensive attention

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