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LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer
BACKGROUND: ALDOA-related specific transcript (ARST) is a recently identified long non-coding RNA (lncRNA) that suppresses glioma progression, while its role in other cancers is unclear. This study explored the role of ARST in colorectal cancer (CRC). METHODS: The present study included 60 CRC patie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8740621/ https://www.ncbi.nlm.nih.gov/pubmed/35018118 http://dx.doi.org/10.2147/CMAR.S338997 |
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author | Dong, Lujia Liu, Di Jing, Dongshuai Xu, Huihui Zhang, Chenxiao Qi, Donglei Liu, Dechun |
author_facet | Dong, Lujia Liu, Di Jing, Dongshuai Xu, Huihui Zhang, Chenxiao Qi, Donglei Liu, Dechun |
author_sort | Dong, Lujia |
collection | PubMed |
description | BACKGROUND: ALDOA-related specific transcript (ARST) is a recently identified long non-coding RNA (lncRNA) that suppresses glioma progression, while its role in other cancers is unclear. This study explored the role of ARST in colorectal cancer (CRC). METHODS: The present study included 60 CRC patients, 60 patients with colon polyps (CP), 60 colitis patients, 60 hemorrhoid patients and 60 healthy controls. All participants were subjected to the collection of plasma, and paired CRC and non-tumor tissues were collected from CRC patients. All samples were subjected to RNA isolation and RT-qPCR to detect the expression of ARST. ROC curve and survival curve analysis were performed to evaluate the diagnostic and prognostic values of plasma ARST for CRC. RESULTS: The expression levels of ARST were lower in CRC plasma samples compared to that in the patient groups and controls (p < 0.01), while other patient groups and controls showed no significant difference. The expression levels of ARST were also lower in CRC tissues compared to that in non-tumor tissues (p < 0.01). Plasma expression levels of ARST effectively distinguished CRC patients from other patients and controls. The expression levels of ARST were closely correlated with patients’ survival. Chi-squared test analysis showed that ARST was closely associated with patients’ distant metastasis but not tumor size. CONCLUSION: ARST is downregulated in CRC, and it might be applied in the diagnosis and prognosis of CRC. |
format | Online Article Text |
id | pubmed-8740621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-87406212022-01-10 LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer Dong, Lujia Liu, Di Jing, Dongshuai Xu, Huihui Zhang, Chenxiao Qi, Donglei Liu, Dechun Cancer Manag Res Original Research BACKGROUND: ALDOA-related specific transcript (ARST) is a recently identified long non-coding RNA (lncRNA) that suppresses glioma progression, while its role in other cancers is unclear. This study explored the role of ARST in colorectal cancer (CRC). METHODS: The present study included 60 CRC patients, 60 patients with colon polyps (CP), 60 colitis patients, 60 hemorrhoid patients and 60 healthy controls. All participants were subjected to the collection of plasma, and paired CRC and non-tumor tissues were collected from CRC patients. All samples were subjected to RNA isolation and RT-qPCR to detect the expression of ARST. ROC curve and survival curve analysis were performed to evaluate the diagnostic and prognostic values of plasma ARST for CRC. RESULTS: The expression levels of ARST were lower in CRC plasma samples compared to that in the patient groups and controls (p < 0.01), while other patient groups and controls showed no significant difference. The expression levels of ARST were also lower in CRC tissues compared to that in non-tumor tissues (p < 0.01). Plasma expression levels of ARST effectively distinguished CRC patients from other patients and controls. The expression levels of ARST were closely correlated with patients’ survival. Chi-squared test analysis showed that ARST was closely associated with patients’ distant metastasis but not tumor size. CONCLUSION: ARST is downregulated in CRC, and it might be applied in the diagnosis and prognosis of CRC. Dove 2022-01-03 /pmc/articles/PMC8740621/ /pubmed/35018118 http://dx.doi.org/10.2147/CMAR.S338997 Text en © 2022 Dong et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Dong, Lujia Liu, Di Jing, Dongshuai Xu, Huihui Zhang, Chenxiao Qi, Donglei Liu, Dechun LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer |
title | LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer |
title_full | LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer |
title_fullStr | LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer |
title_full_unstemmed | LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer |
title_short | LncRNA ARST is a Novel Prognostic and Diagnostic Biomarker for Colorectal Cancer |
title_sort | lncrna arst is a novel prognostic and diagnostic biomarker for colorectal cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8740621/ https://www.ncbi.nlm.nih.gov/pubmed/35018118 http://dx.doi.org/10.2147/CMAR.S338997 |
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