Decoding Cancer Transcriptome Non-Coding RNAs and Beyond

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cell Proliferation and Division".

Deadline for manuscript submissions: closed (30 August 2022) | Viewed by 2058

Special Issue Editor


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Guest Editor
Department of Biosciences, The John van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK
Interests: de-regulated non-coding RNAs in gastrointestinal cancers; DNA methylation in pancreatic cancer; targeting long non-coding RNAs for cancer treatment; mechanisms of chemoresistance in hepatocellular carcinoma; cancer progression and metastasis; tumour-stroma interactions; systems biology; high-throughput approaches.
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Special Issue Information

Dear Colleagues,

The discovery of non-coding RNAs has revitalized the biology field, from the basic to translational research spectrum. Non-coding RNAs (ncRNAs) are functional molecules that are not translated into proteins and comprise almost the 80% of mammalian transcriptome. They have been categorized into different classes, mostly depending on their genomic location, cellular localization, and their size.

NcRNAs are master regulators of gene expression at the transcriptional and/or post-transcriptional level and play fundamental roles in development, tissue/cellular homeostasis, and human pathophysiology. It is now established that ncRNAs work in concert with other epigenetic mechanisms, including DNA methylation and histone modifications, to control gene expression and regulate cancer initiation, growth, and metastasis. Given their cell- and tissue-specific expression patterns, many ncRNAs have emerged as a potential biomarker and therapeutic tool in many types of cancer.

This issue focuses on cutting-edge research across different types of ncRNAs, relevant to cancer and cancer inflammation. We invite authors to submit original, meta-analyses and review articles on basic research, translational and cancer diagnosis or treatment.   

Dr. Maria Hatziapostolou
Guest Editor

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Keywords

  • non-coding RNAs (ncRNAs)
  • microRNAs (miRNAs)
  • long non-coding RNAs (LncRNAs)
  • circular RNAs (circRNAs)
  • transcriptomic analyses
  • cancer diagnosis-biomarkers
  • cancer treatment

Published Papers (1 paper)

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Research

12 pages, 2815 KiB  
Article
LPAL2 Suppresses Tumor Growth and Metastasis of Hepatocellular Carcinoma by Modulating MMP9 Expression
by Yang-Hsiang Lin, Yu-Chin Liu, Cheng-Yi Chen, Hsiang-Cheng Chi, Meng-Han Wu, Po-Shuan Huang, Cheng-Chih Chang, Tzu-Kang Lin, Chau-Ting Yeh and Kwang-Huei Lin
Cells 2022, 11(16), 2610; https://doi.org/10.3390/cells11162610 - 22 Aug 2022
Cited by 3 | Viewed by 1698
Abstract
Tumor metastasis is a complex process modulated by both intrinsic and extrinsic factors that ultimately result in poorer patient outcomes, including diminished survival. Pseudogene-derived long non-coding RNAs (lncRNA) play important roles in cancer progression. In the current study, we found that the pseudogene-derived [...] Read more.
Tumor metastasis is a complex process modulated by both intrinsic and extrinsic factors that ultimately result in poorer patient outcomes, including diminished survival. Pseudogene-derived long non-coding RNAs (lncRNA) play important roles in cancer progression. In the current study, we found that the pseudogene-derived lncRNA LPAL2 is downregulated in hepatocellular carcinoma (HCC) tissues, and further showed that elevated LPAL2 expression is positively correlated with survival outcome. The knockdown of LPAL2 in hepatoma cells induced tumor formation, migration, invasion, sphere formation, and drug resistance. Metalloproteinase 9 (MMP9) was identified as an LPAL2-regulated target gene, consistent with clinical findings that LPAL2 expression is significantly associated with MMP9 expression. Furthermore, patients with a higher expression of LPAL2 and lower expression of MMP9 (LPAL2-high/MMP9-low) had a higher survival rate than those with other combinations. Collectively, our findings establish LPAL2 as a novel tumor suppressor in HCC, and suggest targeting LPAL2 and MMP9 as a therapeutic approach for the treatment of HCC. Full article
(This article belongs to the Special Issue Decoding Cancer Transcriptome Non-Coding RNAs and Beyond)
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