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Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer

Colorectal cancer (CRC) is the second most common cause of cancer-related death globally. Because of a tendency to be an asymptomatic primary tumor and therefore resulting in late detection, most CRC patients are diagnosed in the advanced stage. Several miRNAs have the potential to become novel noni...

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Autores principales: Gil-Kulik, Paulina, Petniak, Alicja, Kluz, Natalia, Wallner, Grzegorz, Skoczylas, Tomasz, Ciechański, Aleksander, Kocki, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531160/
https://www.ncbi.nlm.nih.gov/pubmed/37762323
http://dx.doi.org/10.3390/ijms241814023
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author Gil-Kulik, Paulina
Petniak, Alicja
Kluz, Natalia
Wallner, Grzegorz
Skoczylas, Tomasz
Ciechański, Aleksander
Kocki, Janusz
author_facet Gil-Kulik, Paulina
Petniak, Alicja
Kluz, Natalia
Wallner, Grzegorz
Skoczylas, Tomasz
Ciechański, Aleksander
Kocki, Janusz
author_sort Gil-Kulik, Paulina
collection PubMed
description Colorectal cancer (CRC) is the second most common cause of cancer-related death globally. Because of a tendency to be an asymptomatic primary tumor and therefore resulting in late detection, most CRC patients are diagnosed in the advanced stage. Several miRNAs have the potential to become novel noninvasive biomarkers measured as diagnostic and prognostic indicators of CRC to guide surgical therapies and promote the understanding of the carcinogenesis of CRC. Since the change of miR-3613-3p was associated with several types of cancer other than colorectal cancer, there is a lack of functional evidence and the results are inconsistent. We conducted a pilot microarray study in which we noted a decreased expression of miR-3613-3p in colorectal cancer cells, then we confirmed the expression of miR-3613-3p by qPCR on a group of 83 patients, including 65 patients with colorectal cancer, 5 with a benign tumor and 13 from the control group. We noted that in both malignant and benign tumors, miR-3613-3p is downgraded relative to the surrounding tissue. As a result of the study, we also observed colorectal tumor tissue and surrounding tissue in patients with colorectal cancer who received radiotherapy before surgery, which showed a significantly higher expression of miR-3613-3p compared to patients who did not receive radiotherapy. In addition, we noted that the tissue surrounding the tumor in patients with distant metastases showed a significantly higher expression of miR-3613-3p compared to patients without distant metastases. The increased expression of miR-3613-3p in patients after radiotherapy suggests the possibility of using this miR as a therapeutic target for CRC, but this requires confirmation in further studies.
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spelling pubmed-105311602023-09-28 Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer Gil-Kulik, Paulina Petniak, Alicja Kluz, Natalia Wallner, Grzegorz Skoczylas, Tomasz Ciechański, Aleksander Kocki, Janusz Int J Mol Sci Communication Colorectal cancer (CRC) is the second most common cause of cancer-related death globally. Because of a tendency to be an asymptomatic primary tumor and therefore resulting in late detection, most CRC patients are diagnosed in the advanced stage. Several miRNAs have the potential to become novel noninvasive biomarkers measured as diagnostic and prognostic indicators of CRC to guide surgical therapies and promote the understanding of the carcinogenesis of CRC. Since the change of miR-3613-3p was associated with several types of cancer other than colorectal cancer, there is a lack of functional evidence and the results are inconsistent. We conducted a pilot microarray study in which we noted a decreased expression of miR-3613-3p in colorectal cancer cells, then we confirmed the expression of miR-3613-3p by qPCR on a group of 83 patients, including 65 patients with colorectal cancer, 5 with a benign tumor and 13 from the control group. We noted that in both malignant and benign tumors, miR-3613-3p is downgraded relative to the surrounding tissue. As a result of the study, we also observed colorectal tumor tissue and surrounding tissue in patients with colorectal cancer who received radiotherapy before surgery, which showed a significantly higher expression of miR-3613-3p compared to patients who did not receive radiotherapy. In addition, we noted that the tissue surrounding the tumor in patients with distant metastases showed a significantly higher expression of miR-3613-3p compared to patients without distant metastases. The increased expression of miR-3613-3p in patients after radiotherapy suggests the possibility of using this miR as a therapeutic target for CRC, but this requires confirmation in further studies. MDPI 2023-09-13 /pmc/articles/PMC10531160/ /pubmed/37762323 http://dx.doi.org/10.3390/ijms241814023 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Gil-Kulik, Paulina
Petniak, Alicja
Kluz, Natalia
Wallner, Grzegorz
Skoczylas, Tomasz
Ciechański, Aleksander
Kocki, Janusz
Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer
title Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer
title_full Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer
title_fullStr Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer
title_full_unstemmed Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer
title_short Influence of Clinical Factors on miR-3613-3p Expression in Colorectal Cancer
title_sort influence of clinical factors on mir-3613-3p expression in colorectal cancer
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531160/
https://www.ncbi.nlm.nih.gov/pubmed/37762323
http://dx.doi.org/10.3390/ijms241814023
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