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Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma

Colorectal cancer (CRC) is one of the most common gastrointestinal cancers in the world, and its incidence is increasing all over the world including China. In recent years, research data show that some miRNAs are differentially expressed in cancer tissues, and their expression is closely contribute...

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Autores principales: Li, Junhua, Bulin Baila, Xu, Tian Xiang, Song, Jiang, Su Rina, Wu, Ji, Wang, Tegexibaiyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941573/
https://www.ncbi.nlm.nih.gov/pubmed/35340746
http://dx.doi.org/10.1155/2022/5587084
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author Li, Junhua
Bulin Baila,
Xu, Tian Xiang
Song, Jiang
Su Rina,
Wu, Ji
Wang, Tegexibaiyin
author_facet Li, Junhua
Bulin Baila,
Xu, Tian Xiang
Song, Jiang
Su Rina,
Wu, Ji
Wang, Tegexibaiyin
author_sort Li, Junhua
collection PubMed
description Colorectal cancer (CRC) is one of the most common gastrointestinal cancers in the world, and its incidence is increasing all over the world including China. In recent years, research data show that some miRNAs are differentially expressed in cancer tissues, and their expression is closely contributed with the prognosis of CRC. Microarray technology was used, and 179 miRNAs were screened out with significantly altered expression in CRC tissues compared with adjacent tissues. The expression of mir-145-5p in tumor tissues was 3.48 times lower than that in normal tissues. Using bioinformatics technology and network resource prediction, we found that mir-145-5p had a potential target gene relationship with msln gene. Then, qRT-PCR was used to validate the expression level of mir-145-5p and msln mRNA in CRC and paracancerous tissues. The results showed that msln mRNA was higher than in normal tissues, while mir-145-5p was lower, with statistically significant difference (P < 0.01, n = 3). Furthermore, the expression of msln protein in CRC and normal colorectal tissues was detected by protein mass spectrometry (MRM) (n = 3) and immunohistochemistry in a total case of 30 colorectal cancer tissues and normal tissues. Result showed that the positive expression of msln in CRC was higher than that in normal colorectal tissues, 1.38e-6 and 1.89e-6, respectively (P < 0.01, n = 3). Furthermore, in 48 h RTCA real-time monitoring experiment, mir-145-5p showed inhibitory effect on the proliferation of colo320 cells stimulated by msln. This study demonstrated that msln is a target gene of mir-145-5p in CRC. Besides, mir-145-5p negatively regulates the proliferation of CRC colo320 cells through downregulating msln gene expression in CRC colo320 cells.
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spelling pubmed-89415732022-03-24 Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma Li, Junhua Bulin Baila, Xu, Tian Xiang Song, Jiang Su Rina, Wu, Ji Wang, Tegexibaiyin Anal Cell Pathol (Amst) Research Article Colorectal cancer (CRC) is one of the most common gastrointestinal cancers in the world, and its incidence is increasing all over the world including China. In recent years, research data show that some miRNAs are differentially expressed in cancer tissues, and their expression is closely contributed with the prognosis of CRC. Microarray technology was used, and 179 miRNAs were screened out with significantly altered expression in CRC tissues compared with adjacent tissues. The expression of mir-145-5p in tumor tissues was 3.48 times lower than that in normal tissues. Using bioinformatics technology and network resource prediction, we found that mir-145-5p had a potential target gene relationship with msln gene. Then, qRT-PCR was used to validate the expression level of mir-145-5p and msln mRNA in CRC and paracancerous tissues. The results showed that msln mRNA was higher than in normal tissues, while mir-145-5p was lower, with statistically significant difference (P < 0.01, n = 3). Furthermore, the expression of msln protein in CRC and normal colorectal tissues was detected by protein mass spectrometry (MRM) (n = 3) and immunohistochemistry in a total case of 30 colorectal cancer tissues and normal tissues. Result showed that the positive expression of msln in CRC was higher than that in normal colorectal tissues, 1.38e-6 and 1.89e-6, respectively (P < 0.01, n = 3). Furthermore, in 48 h RTCA real-time monitoring experiment, mir-145-5p showed inhibitory effect on the proliferation of colo320 cells stimulated by msln. This study demonstrated that msln is a target gene of mir-145-5p in CRC. Besides, mir-145-5p negatively regulates the proliferation of CRC colo320 cells through downregulating msln gene expression in CRC colo320 cells. Hindawi 2022-03-15 /pmc/articles/PMC8941573/ /pubmed/35340746 http://dx.doi.org/10.1155/2022/5587084 Text en Copyright © 2022 Junhua Li et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Junhua
Bulin Baila,
Xu, Tian Xiang
Song, Jiang
Su Rina,
Wu, Ji
Wang, Tegexibaiyin
Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma
title Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma
title_full Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma
title_fullStr Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma
title_full_unstemmed Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma
title_short Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma
title_sort effects of hsa-mir-145-5p on the regulation of msln expression in colorectal adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941573/
https://www.ncbi.nlm.nih.gov/pubmed/35340746
http://dx.doi.org/10.1155/2022/5587084
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