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High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients
BACKGROUND: Gastric cancer (GC) remains an aggressive malignancy with a high rate of mortality, being the third leading cause of cancer-related death. More than one million newly diagnosed cases and 782685 deaths due to GC were reported in 2018. GC is characterized by limited effective treatment opt...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304107/ https://www.ncbi.nlm.nih.gov/pubmed/32587446 http://dx.doi.org/10.3748/wjg.v26.i22.3024 |
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author | Necula, Laura Matei, Lilia Dragu, Denisa Pitica, Ioana Neagu, Ana Iulia Bleotu, Coralia Dima, Simona Popescu, Irinel Diaconu, Carmen C Chivu-Economescu, Mihaela |
author_facet | Necula, Laura Matei, Lilia Dragu, Denisa Pitica, Ioana Neagu, Ana Iulia Bleotu, Coralia Dima, Simona Popescu, Irinel Diaconu, Carmen C Chivu-Economescu, Mihaela |
author_sort | Necula, Laura |
collection | PubMed |
description | BACKGROUND: Gastric cancer (GC) remains an aggressive malignancy with a high rate of mortality, being the third leading cause of cancer-related death. More than one million newly diagnosed cases and 782685 deaths due to GC were reported in 2018. GC is characterized by limited effective treatment options and the lack of consistent biomarkers for the diagnosis and prognosis of these patients. The discovery of new biomarkers useful in the early diagnosis of GC is mandatory. AIM: To evaluate the potential of COL10A1 as a circulating biomarker for the diagnosis and prognosis of gastric adenocarcinoma patients. METHODS: Plasma and tissue obtained from 49 patients with gastric adenocarcinoma have been used in exploring the expression of COL10A1. Real-time PCR and western blot techniques were used to evaluate COL10A1 level in gastric tumor tissue compared to normal adjacent tissue. The circulating level of COL10A1 was also evaluated by ELISA in plasma of gastric adenocarcinoma patients. Survival analysis was made in order to evaluate the potential of COL10A1 as a biomarker for the diagnosis and prognosis of gastric adenocarcinoma patients. RESULTS: Our results showed a significant increase in COL10A1 gene expression and protein levels in gastric tumor tissue compared to adjacent normal tissue (P < 0.05). COL10A1 seems to show an elevated expression from the beginning of carcinogenesis, in the early stages, and its increased level remains elevated during cancer progression. A significant increase of COL10A1 plasma level in gastric adenocarcinoma patients was also identified. Moreover, increased COL10A1 plasma level was associated with poor survival of the patients. Plasma COL10A1 performed a diagnostic value in GC with area under the receiver operating characteristic curve (AUC) of 0.9171 (P = 0.0002), sensitivity of 87.76%, and specificity of 100.0%. Furthermore, this study demonstrated the potential role of plasma COL10A1 in the early detection of GC, as in the early stage, we obtained an AUC of 0.8789 (P = 0.0030), sensitivity of 81.25%, and specificity of 100.0%. CONCLUSION: Circulating expression level of COL10A1 is significantly increased in gastric adenocarcinoma patients being associated with poor survival and is a potential biomarker for early detection of GC. |
format | Online Article Text |
id | pubmed-7304107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-73041072020-06-24 High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients Necula, Laura Matei, Lilia Dragu, Denisa Pitica, Ioana Neagu, Ana Iulia Bleotu, Coralia Dima, Simona Popescu, Irinel Diaconu, Carmen C Chivu-Economescu, Mihaela World J Gastroenterol Basic Study BACKGROUND: Gastric cancer (GC) remains an aggressive malignancy with a high rate of mortality, being the third leading cause of cancer-related death. More than one million newly diagnosed cases and 782685 deaths due to GC were reported in 2018. GC is characterized by limited effective treatment options and the lack of consistent biomarkers for the diagnosis and prognosis of these patients. The discovery of new biomarkers useful in the early diagnosis of GC is mandatory. AIM: To evaluate the potential of COL10A1 as a circulating biomarker for the diagnosis and prognosis of gastric adenocarcinoma patients. METHODS: Plasma and tissue obtained from 49 patients with gastric adenocarcinoma have been used in exploring the expression of COL10A1. Real-time PCR and western blot techniques were used to evaluate COL10A1 level in gastric tumor tissue compared to normal adjacent tissue. The circulating level of COL10A1 was also evaluated by ELISA in plasma of gastric adenocarcinoma patients. Survival analysis was made in order to evaluate the potential of COL10A1 as a biomarker for the diagnosis and prognosis of gastric adenocarcinoma patients. RESULTS: Our results showed a significant increase in COL10A1 gene expression and protein levels in gastric tumor tissue compared to adjacent normal tissue (P < 0.05). COL10A1 seems to show an elevated expression from the beginning of carcinogenesis, in the early stages, and its increased level remains elevated during cancer progression. A significant increase of COL10A1 plasma level in gastric adenocarcinoma patients was also identified. Moreover, increased COL10A1 plasma level was associated with poor survival of the patients. Plasma COL10A1 performed a diagnostic value in GC with area under the receiver operating characteristic curve (AUC) of 0.9171 (P = 0.0002), sensitivity of 87.76%, and specificity of 100.0%. Furthermore, this study demonstrated the potential role of plasma COL10A1 in the early detection of GC, as in the early stage, we obtained an AUC of 0.8789 (P = 0.0030), sensitivity of 81.25%, and specificity of 100.0%. CONCLUSION: Circulating expression level of COL10A1 is significantly increased in gastric adenocarcinoma patients being associated with poor survival and is a potential biomarker for early detection of GC. Baishideng Publishing Group Inc 2020-06-14 2020-06-14 /pmc/articles/PMC7304107/ /pubmed/32587446 http://dx.doi.org/10.3748/wjg.v26.i22.3024 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Basic Study Necula, Laura Matei, Lilia Dragu, Denisa Pitica, Ioana Neagu, Ana Iulia Bleotu, Coralia Dima, Simona Popescu, Irinel Diaconu, Carmen C Chivu-Economescu, Mihaela High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients |
title | High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients |
title_full | High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients |
title_fullStr | High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients |
title_full_unstemmed | High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients |
title_short | High plasma levels of COL10A1 are associated with advanced tumor stage in gastric cancer patients |
title_sort | high plasma levels of col10a1 are associated with advanced tumor stage in gastric cancer patients |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304107/ https://www.ncbi.nlm.nih.gov/pubmed/32587446 http://dx.doi.org/10.3748/wjg.v26.i22.3024 |
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