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A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2
Atherosclerosis (AS) is a potential inducer of numerous cardio-cerebrovascular diseases. However, little research has investigated the expression of TPM2 in human atherosclerosis samples. A total of 34 clinical samples were obtained, including 17 atherosclerosis and 17 normal artery samples, between...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947840/ https://www.ncbi.nlm.nih.gov/pubmed/35371599 http://dx.doi.org/10.14336/AD.2021.0926 |
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author | Meng, Ling-bing Xu, Hong-xuan Shan, Meng-jie Hu, Gai-feng Liu, Long-teng Chen, Yu-hui Liu, Yun-qing Wang, Li Chen, Zuoguan Li, Yong-jun Gong, Tao Liu, De-ping |
author_facet | Meng, Ling-bing Xu, Hong-xuan Shan, Meng-jie Hu, Gai-feng Liu, Long-teng Chen, Yu-hui Liu, Yun-qing Wang, Li Chen, Zuoguan Li, Yong-jun Gong, Tao Liu, De-ping |
author_sort | Meng, Ling-bing |
collection | PubMed |
description | Atherosclerosis (AS) is a potential inducer of numerous cardio-cerebrovascular diseases. However, little research has investigated the expression of TPM2 in human atherosclerosis samples. A total of 34 clinical samples were obtained, including 17 atherosclerosis and 17 normal artery samples, between January 2018 and April 2021. Bioinformatics analysis was applied to explore the potential role of TPM2 in atherosclerosis. Immunohistochemistry, immunofluorescence, and western blotting assays were used to detect the expression of TPM2 and α-SMA proteins. The mRNA expression levels of TPM2 and α-SMA were detected using RT-qPCR. A neural network and intima-media thickness model were constructed. A strong relationship existed between the intima-media thickness and relative protein expression of TPM2 (P<0.001, R=-0.579). The expression of TPM2 was lower in atherosclerosis than normal artery (P<0.05). Univariate logistic regression showed that TPM2 (OR=0.150, 95% CI: 0.026-0.868, P=0.034) had clear correlations with atherosclerosis. A neural network model was successfully constructed with a relativity of 0.94434. TPM2 might be an independent protective factor for arteries, and one novel biomarker of atherosclerosis. |
format | Online Article Text |
id | pubmed-8947840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-89478402022-04-01 A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 Meng, Ling-bing Xu, Hong-xuan Shan, Meng-jie Hu, Gai-feng Liu, Long-teng Chen, Yu-hui Liu, Yun-qing Wang, Li Chen, Zuoguan Li, Yong-jun Gong, Tao Liu, De-ping Aging Dis Opinion Atherosclerosis (AS) is a potential inducer of numerous cardio-cerebrovascular diseases. However, little research has investigated the expression of TPM2 in human atherosclerosis samples. A total of 34 clinical samples were obtained, including 17 atherosclerosis and 17 normal artery samples, between January 2018 and April 2021. Bioinformatics analysis was applied to explore the potential role of TPM2 in atherosclerosis. Immunohistochemistry, immunofluorescence, and western blotting assays were used to detect the expression of TPM2 and α-SMA proteins. The mRNA expression levels of TPM2 and α-SMA were detected using RT-qPCR. A neural network and intima-media thickness model were constructed. A strong relationship existed between the intima-media thickness and relative protein expression of TPM2 (P<0.001, R=-0.579). The expression of TPM2 was lower in atherosclerosis than normal artery (P<0.05). Univariate logistic regression showed that TPM2 (OR=0.150, 95% CI: 0.026-0.868, P=0.034) had clear correlations with atherosclerosis. A neural network model was successfully constructed with a relativity of 0.94434. TPM2 might be an independent protective factor for arteries, and one novel biomarker of atherosclerosis. JKL International LLC 2022-04-01 /pmc/articles/PMC8947840/ /pubmed/35371599 http://dx.doi.org/10.14336/AD.2021.0926 Text en Copyright: © 2022 Meng et al. https://creativecommons.org/licenses/by/2.0/this is an open access article distributed under the terms of the creative commons attribution license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Opinion Meng, Ling-bing Xu, Hong-xuan Shan, Meng-jie Hu, Gai-feng Liu, Long-teng Chen, Yu-hui Liu, Yun-qing Wang, Li Chen, Zuoguan Li, Yong-jun Gong, Tao Liu, De-ping A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 |
title | A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 |
title_full | A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 |
title_fullStr | A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 |
title_full_unstemmed | A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 |
title_short | A Potential Target for Clinical Atherosclerosis: A Novel Insight Derived from TPM2 |
title_sort | potential target for clinical atherosclerosis: a novel insight derived from tpm2 |
topic | Opinion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947840/ https://www.ncbi.nlm.nih.gov/pubmed/35371599 http://dx.doi.org/10.14336/AD.2021.0926 |
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