MicroRNA in Cancer and Neurodegenerative Disorders

A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Molecular Genetics and Genomics".

Deadline for manuscript submissions: closed (20 February 2023) | Viewed by 2733

Special Issue Editors


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Guest Editor
Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, L’Aquila, Italy
Interests: general and molecular pathology; cancer molecular pathogenesis; microRNA; cell cycle; apoptosis; inflammation
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, L’Aquila, Italy
Interests: cancer molecular pathogenesis; inflammation; NF-kB signaling; apoptosis; preclinical models; new therapeutic targets identification; epatocarcinogenesis; neurodegenerative eye and ear diseases; microRNA

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Guest Editor
Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, L’Aquila, Italy
Interests: cancer molecular pathogenesis and diagnostics; personalized medicine; epatocarcinogenesis; neurodegenerative eye and ear diseases; microRNA; profiling analysis; bioinformatics

E-Mail Website
Guest Editor
Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, Via Vetoio, 67100 L’Aquila, Italy
Interests: familial breast cancer; oncogenes and tumor suppressor genes; microRNA expression analysis; circulating biomarkers

Special Issue Information

Dear Colleagues, 

MicroRNAs are short, non-coding RNAs able to fine-tune gene expression at the post-transcriptional level, and are involved in the control of fundamental cell processes such as growth, proliferation, differentiation, cell cycle and apoptosis. Dysregulated expression levels of microRNAs have been described in cancer and neurodegenerative diseases, known to be major public health issues. Tumor initiation, progression and metastasis dissemination are correlated to significant changes in gene expression, and an increasing number of studies has focused on examining, in depth, the role of microRNAs in tumorigenesis. Depending on the functions of target genes, microRNAs can show tumor-promoting or suppressive properties by regulating the expression of entire groups of genes implicated in oncogenesis and metastasis. Biogenesis disruption and altered levels of miRNAs have been widely described in neurodegenerative disorders as well, evidencing the relevant involvement of these molecules in the pathogenesis of such diseases. Furthermore, microRNAs are considered as potentially suitable tissue or circulating non-invasive diagnostic, prognostic and predictive biomarkers, as they are released from tissues by active (exosomes and vesicles) or passive (apoptosis and necrosis) mechanisms into the bloodstream, where they are stable and resistant to endogenous RNase. Moreover, these short molecules are thought to have a potential therapeutic value, and the development of innovative strategies aimed at restoring levels of dysregulated/aberrantly expressed miRNAs constitutes a great challenge for the improvement of cancer and neurodegenerative disorder treatments.

In this Special Issue, we are interested in recent advances and opinions regarding the role of microRNAs in cancer and neurodegenerative diseases, research papers and reviews focused on, but not limited to, the role of microRNAs in the pathogenesis of the above-mentioned diseases, microRNAs as biomarkers, limitations and challenges of the possible therapeutic use of microRNAs and strategies to restore microRNA expression levels, microRNA preclinical models and bioinformatics approaches for miRNAs/target gene analysis.

Prof. Dr. Edoardo Alesse
Dr. Francesca Zazzeroni
Dr. Alessandra Tessitore
Dr. Veronica Zelli
Guest Editors

Manuscript Submission Information

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Keywords

  • non-coding RNAs
  • cancer
  • neurodegenerative diseases
  • biomarkers
  • preclinical models
  • targetome
  • microRNA-based therapy

Published Papers (1 paper)

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Review

18 pages, 3545 KiB  
Review
The Double Face of miR-708: A Pan-Cancer Player with Dissociative Identity Disorder
by Jaqueline Carvalho de Oliveira, Carolina Mathias, Verônica Cristina Oliveira, Julia Alejandra Pezuk and María Sol Brassesco
Genes 2022, 13(12), 2375; https://doi.org/10.3390/genes13122375 - 16 Dec 2022
Cited by 2 | Viewed by 2118
Abstract
Over the last decades, accumulating evidence has shown tumor-dependent profiles of miR-708, being either up- or downregulated, and thus, acting as a “Janus” regulator of oncogenic pathways. Herein, its functional duality was assessed through a thorough review of the literature and further validation [...] Read more.
Over the last decades, accumulating evidence has shown tumor-dependent profiles of miR-708, being either up- or downregulated, and thus, acting as a “Janus” regulator of oncogenic pathways. Herein, its functional duality was assessed through a thorough review of the literature and further validation in silico using The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. In the literature, miR-708 was found with an oncogenic role in eight tumor types, while a suppressor tumor role was described in seven cancers. This double profile was also found in TCGA and GEO databases, with some tumor types having a high expression of miR-708 and others with low expression compared with non-tumor counterparts. The investigation of validated targets using miRBase, miRTarBase, and miRecords platforms, identified a total of 572 genes that appeared enriched for PI3K-Akt signaling, followed by cell cycle control, p53, Apellin and Hippo signaling, endocrine resistance, focal adhesion, and cell senescence regulations, which are all recognized contributors of tumoral phenotypes. Among these targets, a set of 15 genes shared by at least two platforms was identified, most of which have important roles in cancer cells that influence either tumor suppression or progression. In a clinical scenario, miR-708 has shown to be a good diagnostic and prognosis marker. However, its multitarget nature and opposing roles in diverse human tumors, aligned with insufficient experimental data and the lack of proper delivery strategies, hamper its potential as a sequence-directed therapeutic. Full article
(This article belongs to the Special Issue MicroRNA in Cancer and Neurodegenerative Disorders)
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