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Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma

Carcinoma ex pleomorphic adenoma (CXPA) is a rare malignancy that transforms from PA. Early detection of the carcinoma by biopsy is difficult due to similar histopathology of the malignant and benign components. To address this, we investigated and compared the characteristic miRNA expression patter...

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Autores principales: Kim, Hyojin, Eun, Shin, Jeong, Woo-Jin, Ahn, Soon-Hyun, Bae, Yun Jung, Lee, Joong Seob, Kim, Heejin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352753/
https://www.ncbi.nlm.nih.gov/pubmed/35927424
http://dx.doi.org/10.1038/s41598-022-17740-9
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author Kim, Hyojin
Eun, Shin
Jeong, Woo-Jin
Ahn, Soon-Hyun
Bae, Yun Jung
Lee, Joong Seob
Kim, Heejin
author_facet Kim, Hyojin
Eun, Shin
Jeong, Woo-Jin
Ahn, Soon-Hyun
Bae, Yun Jung
Lee, Joong Seob
Kim, Heejin
author_sort Kim, Hyojin
collection PubMed
description Carcinoma ex pleomorphic adenoma (CXPA) is a rare malignancy that transforms from PA. Early detection of the carcinoma by biopsy is difficult due to similar histopathology of the malignant and benign components. To address this, we investigated and compared the characteristic miRNA expression patterns across samples of the PA, carcinomatous portions (CA) of CXPA, as well as conventional PA. We selected 13 CXPA and 16 conventional PA FFPE samples, separated the PA and CA portions of CXPA samples and conducted miRNA profiling for each group. Among 13 transcripts that were differentially expressed between PA and CA of CXPA, eight miRNAs were up-regulated and five down-regulated in CA. Bioinformatic analysis revealed that the up-regulated miRNAs were related to cancer progression and down-regulated ones to tumor suppression. Additionally, seven miRNAs were significantly up-regulated in PA of CXPA compared to conventional PA, although they are histopathologically similar. Almost all of these transcripts interacted with TP53, a well-known tumor suppressor. In conclusion, we identified differentially expressed miRNAs in PA and CA of CXPA, which were closely associated with TP53 and various cancer-related pathways. We also identified differentially expressed miRNAs in the PA of CXPA and conventional PA which may serve as potential biomarkers.
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spelling pubmed-93527532022-08-06 Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma Kim, Hyojin Eun, Shin Jeong, Woo-Jin Ahn, Soon-Hyun Bae, Yun Jung Lee, Joong Seob Kim, Heejin Sci Rep Article Carcinoma ex pleomorphic adenoma (CXPA) is a rare malignancy that transforms from PA. Early detection of the carcinoma by biopsy is difficult due to similar histopathology of the malignant and benign components. To address this, we investigated and compared the characteristic miRNA expression patterns across samples of the PA, carcinomatous portions (CA) of CXPA, as well as conventional PA. We selected 13 CXPA and 16 conventional PA FFPE samples, separated the PA and CA portions of CXPA samples and conducted miRNA profiling for each group. Among 13 transcripts that were differentially expressed between PA and CA of CXPA, eight miRNAs were up-regulated and five down-regulated in CA. Bioinformatic analysis revealed that the up-regulated miRNAs were related to cancer progression and down-regulated ones to tumor suppression. Additionally, seven miRNAs were significantly up-regulated in PA of CXPA compared to conventional PA, although they are histopathologically similar. Almost all of these transcripts interacted with TP53, a well-known tumor suppressor. In conclusion, we identified differentially expressed miRNAs in PA and CA of CXPA, which were closely associated with TP53 and various cancer-related pathways. We also identified differentially expressed miRNAs in the PA of CXPA and conventional PA which may serve as potential biomarkers. Nature Publishing Group UK 2022-08-04 /pmc/articles/PMC9352753/ /pubmed/35927424 http://dx.doi.org/10.1038/s41598-022-17740-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kim, Hyojin
Eun, Shin
Jeong, Woo-Jin
Ahn, Soon-Hyun
Bae, Yun Jung
Lee, Joong Seob
Kim, Heejin
Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma
title Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma
title_full Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma
title_fullStr Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma
title_full_unstemmed Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma
title_short Identification of differentially expressed microRNAs as potential biomarkers for carcinoma ex pleomorphic adenoma
title_sort identification of differentially expressed micrornas as potential biomarkers for carcinoma ex pleomorphic adenoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352753/
https://www.ncbi.nlm.nih.gov/pubmed/35927424
http://dx.doi.org/10.1038/s41598-022-17740-9
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