miRNA in Colorectal Cancer

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Biomarkers".

Deadline for manuscript submissions: 30 November 2024 | Viewed by 1374

Special Issue Editor


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Guest Editor
Hospital Clínico San Carlos, 28040 Madrid, Spain
Interests: colorectal cancer; molecular mechanisms

Special Issue Information

Dear Colleagues,

Colorectal cancer represents a major health problem, being the third leading cause of death in developed countries. MicroRNAs (miRs) regulate gene activity post-transcriptionally through the inhibition of protein translation. In cancer, they can function as oncogenes or as tumor suppressors, and miR signatures can serve as promising biomarkers for diagnosis, prognosis, and treatment efficacy monitoring over the disease course. Recently, another class of small RNAs, the tRNA-derived small RNA (tsRNA), is generating increasing interest in cancer research. Transfer-RNA-derived small RNA reproduce miRNAs’ mechanisms of action by interacting with Argonaute (AGO) to inhibit protein translation.  Both miRNAs and tsRNAs have been shown to play essential roles in malignant transformation, cell proliferation, migration and apoptosis. MicroRNAs and tsRNAs can be analyzed not only from solid tissues, but their small size and robustness in serum make them excellent candidates to be measured in fluids, including blood/plasma/serum, urine, or saliva. An accurate determination of miRNAs or tsRNAs in FFPE samples and, particularly, in biofluids, is complicated by their small size, high degree of homology, and need for their extraction. Therefore, these efforts require well-standardized and accurate procedures.

This Special Issue is dedicated to the following main topics in colorectal cancer:

  • miRNAs or tsRNAs as diagnostic, prognostic and/or predictive biomarkers.
  • Evaluation and comparison of different methodologies for accurate analysis of miRNAs and tsRNAs.
  • Implications of miRNAs or tsRNAs in molecular mechanism studies carried out in cell lines or mouse models.
  • Tumor subtyping based on miRNA or tsRNA expression analysis.
  • The use of genomics and transcriptomics for the identification of novel miRNA/tsRNAs signatures.

We are pleased to invite you to contribute to this Special Issue with submissions of original research articles, reviews or metanalyses related to this subject.

Dr. Beatriz Perez-Villamil
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • colorectal cancer
  • miRNAs
  • tsRNAs
  • molecular classification
  • molecular mechanisms
  • prognostic/predictive biomarkers
  • genomics
  • transcriptomics

Published Papers (1 paper)

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Research

15 pages, 1035 KiB  
Article
Expression Analysis of hsa-miR-181a-5p, hsa-miR-143-3p, hsa-miR-132-3p and hsa-miR-23a-3p as Biomarkers in Colorectal Cancer—Relationship to the Body Mass Index
by Sofía Elena Tesolato, Daniel González-Gamo, Ana Barabash, Paula Claver, Sofía Cristina de la Serna, Inmaculada Domínguez-Serrano, Jana Dziakova, Carmen de Juan, Antonio José Torres and Pilar Iniesta
Cancers 2023, 15(13), 3324; https://doi.org/10.3390/cancers15133324 - 24 Jun 2023
Viewed by 1132
Abstract
This work aims to investigate the expression levels of four preselected miRNAs previously linked to cancer and/or obesity, with the purpose of finding potential biomarkers in the clinical management of CRC developed by patients showing different BMI values. We analyzed samples from a [...] Read more.
This work aims to investigate the expression levels of four preselected miRNAs previously linked to cancer and/or obesity, with the purpose of finding potential biomarkers in the clinical management of CRC developed by patients showing different BMI values. We analyzed samples from a total of 65 subjects: 43 affected by CRC and 22 without cancer. Serum and both subcutaneous and omental adipose tissues (SAT and OAT) were investigated, as well as tumor and non-tumor colorectal tissues in the case of the CRC patients. The relative expression (2−∆∆Ct) levels of 4 miRNAs (hsa-miR-181a-5p, hsa-miR-143-3p, has-miR-132-3p and hsa-miR-23a-3p) were measured by RT-qPCR. Serum, SAT and OAT expression levels of these miRNAs showed significant differences between subjects with and without CRC, especially in the group of overweight/obese subjects. In CRC, serum levels of hsa-miR-143-3p clearly correlated with their levels in both SAT and OAT, independently of the BMI group. Moreover, hsa-miR-181a-5p could be considered as a biomarker in CRC patients with BMI ≥ 25 Kg/m2 and emerges as a tumor location marker. We conclude that both adiposity and CRC induce changes in the expression of the miRNAs investigated, and hsa-miR-143-3p and hsa-miR-181a-5p expression analysis could be useful in the clinical management of CRC. Full article
(This article belongs to the Special Issue miRNA in Colorectal Cancer)
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