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Different primers for diagnosing circulating cell-free DNA of colorectal cancer
BACKGROUND: Cell-free DNA (cfDNA) primers have been designed to screen for cancer diagnosis, but the results have been inconsistent. The study aimed to compare different primers for diagnosing cfDNA of colorectal cancer (CRC). METHODS: Peripheral blood specimens were collected from 71 patients with...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798792/ https://www.ncbi.nlm.nih.gov/pubmed/35117709 http://dx.doi.org/10.21037/tcr-19-2017 |
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author | Shi, Hao Li, Qigang Liao, Juan Bai, Lian Wu, Shuai Xie, Jian He, Gan |
author_facet | Shi, Hao Li, Qigang Liao, Juan Bai, Lian Wu, Shuai Xie, Jian He, Gan |
author_sort | Shi, Hao |
collection | PubMed |
description | BACKGROUND: Cell-free DNA (cfDNA) primers have been designed to screen for cancer diagnosis, but the results have been inconsistent. The study aimed to compare different primers for diagnosing cfDNA of colorectal cancer (CRC). METHODS: Peripheral blood specimens were collected from 71 patients with CRC and 20 patients with proliferative intestinal polyps. Quantitative polymerase chain reaction (q-PCR) was used to detect the concentration of cfDNA of these primers, including ALU elements (ALU), Beta-actin (ACTB), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The receiver operator characteristic curve (ROC) was performed to analyze the diagnostic value. RESULTS: The concentration of cfDNA in plasma of the CRC group determined by primers ALU and GAPDH was significantly higher than that of the intestinal polyp group (P<0.05). There was no significant difference in cfDNA level determined by primer ACTB between the CRC group and the intestinal polyp group (P>0.05). The area under curves (AUCs) of ALU, GAPDH, and ACTB were 0.734, 0.800, and 0.503, respectively. CONCLUSIONS: The GAPDH and ALU in plasma are expected to be sensitive indicators for the diagnosis of CRC. |
format | Online Article Text |
id | pubmed-8798792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87987922022-02-02 Different primers for diagnosing circulating cell-free DNA of colorectal cancer Shi, Hao Li, Qigang Liao, Juan Bai, Lian Wu, Shuai Xie, Jian He, Gan Transl Cancer Res Original Article BACKGROUND: Cell-free DNA (cfDNA) primers have been designed to screen for cancer diagnosis, but the results have been inconsistent. The study aimed to compare different primers for diagnosing cfDNA of colorectal cancer (CRC). METHODS: Peripheral blood specimens were collected from 71 patients with CRC and 20 patients with proliferative intestinal polyps. Quantitative polymerase chain reaction (q-PCR) was used to detect the concentration of cfDNA of these primers, including ALU elements (ALU), Beta-actin (ACTB), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The receiver operator characteristic curve (ROC) was performed to analyze the diagnostic value. RESULTS: The concentration of cfDNA in plasma of the CRC group determined by primers ALU and GAPDH was significantly higher than that of the intestinal polyp group (P<0.05). There was no significant difference in cfDNA level determined by primer ACTB between the CRC group and the intestinal polyp group (P>0.05). The area under curves (AUCs) of ALU, GAPDH, and ACTB were 0.734, 0.800, and 0.503, respectively. CONCLUSIONS: The GAPDH and ALU in plasma are expected to be sensitive indicators for the diagnosis of CRC. AME Publishing Company 2020-05 /pmc/articles/PMC8798792/ /pubmed/35117709 http://dx.doi.org/10.21037/tcr-19-2017 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Shi, Hao Li, Qigang Liao, Juan Bai, Lian Wu, Shuai Xie, Jian He, Gan Different primers for diagnosing circulating cell-free DNA of colorectal cancer |
title | Different primers for diagnosing circulating cell-free DNA of colorectal cancer |
title_full | Different primers for diagnosing circulating cell-free DNA of colorectal cancer |
title_fullStr | Different primers for diagnosing circulating cell-free DNA of colorectal cancer |
title_full_unstemmed | Different primers for diagnosing circulating cell-free DNA of colorectal cancer |
title_short | Different primers for diagnosing circulating cell-free DNA of colorectal cancer |
title_sort | different primers for diagnosing circulating cell-free dna of colorectal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798792/ https://www.ncbi.nlm.nih.gov/pubmed/35117709 http://dx.doi.org/10.21037/tcr-19-2017 |
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