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LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer

BACKGROUND: It has been reported that long non-coding RNAs (lncRNAs) can be regarded as a biomarker and had particular clinical significance for early screening and gastric cancer (GC) diagnosis. Therefore, this study aimed to investigate whether serum HCP5 could be a new diagnostic biomarker. METHO...

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Autores principales: Qin, Shiyi, Yang, Lei, Kong, Shan, Xu, Yanhua, Liang, Bo, Ju, Shaoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252797/
https://www.ncbi.nlm.nih.gov/pubmed/34222007
http://dx.doi.org/10.3389/fonc.2021.684531
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author Qin, Shiyi
Yang, Lei
Kong, Shan
Xu, Yanhua
Liang, Bo
Ju, Shaoqing
author_facet Qin, Shiyi
Yang, Lei
Kong, Shan
Xu, Yanhua
Liang, Bo
Ju, Shaoqing
author_sort Qin, Shiyi
collection PubMed
description BACKGROUND: It has been reported that long non-coding RNAs (lncRNAs) can be regarded as a biomarker and had particular clinical significance for early screening and gastric cancer (GC) diagnosis. Therefore, this study aimed to investigate whether serum HCP5 could be a new diagnostic biomarker. METHODS: Filtered out the HCP5 from the GEO database. The specificity of HCP5 was verified by real-time fluorescence quantitative PCR (qRT-PCR), and then the stability of HCP5 was verified by room temperature storage and repeated freeze-thaw experiments. Meanwhile, the accuracy of HCP5 was verified by agarose gel electrophoresis (AGE) and Sanger sequencing. Simultaneously, the expression level of serum HCP5 was detected by qRT-PCR in 98 patients with primary gastric cancer, 21 gastritis patients, 82 healthy donors, and multiple cancer types. Then, the methodology analysis was carried on. Moreover, receiver operating characteristic (ROC) was used to evaluate its diagnostic efficiency. RESULTS: qRT-PCR method had good repeatability and stability in detecting HCP5. The expression level of HCP5 in the serum of gastric cancer patients was remarkably higher than that of healthy controls, and it could distinguish gastritis patients from healthy donors. Besides, the expression of HCP5 was increased dramatically in MKN-45 and MGC-803. The FISH assay showed that HCP5 was mainly distributed in the cytoplasm of MKN-45 and BGC-823 cells. When HCP5 was combined with existing tumor markers, the diagnostic efficiency of HCP5 was the best, and the combined diagnosis of carcinoembryonic antigen (CEA), carbohydrate antigen199 (CA199), and HCP5 can significantly improve the diagnostic sensitivity. Besides, compared with the expression levels of thyroid cancer (THCA), colorectal cancer (CRC), and breast cancer (BRCA), serum HCP5 in gastric cancer was the most specific. Moreover, the high expression of serum HCP5 was related to differentiation, lymph node metastasis, and nerve invasion. The term of serum HCP5 after the operation was significantly lower than that of patients with primary gastric cancer. CONCLUSION: Serum HCP5 can be used as a potential biomarker of non-invasive fluid biopsy, which had a unique value in the early diagnosis, development, and prognosis of gastric cancer.
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spelling pubmed-82527972021-07-03 LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer Qin, Shiyi Yang, Lei Kong, Shan Xu, Yanhua Liang, Bo Ju, Shaoqing Front Oncol Oncology BACKGROUND: It has been reported that long non-coding RNAs (lncRNAs) can be regarded as a biomarker and had particular clinical significance for early screening and gastric cancer (GC) diagnosis. Therefore, this study aimed to investigate whether serum HCP5 could be a new diagnostic biomarker. METHODS: Filtered out the HCP5 from the GEO database. The specificity of HCP5 was verified by real-time fluorescence quantitative PCR (qRT-PCR), and then the stability of HCP5 was verified by room temperature storage and repeated freeze-thaw experiments. Meanwhile, the accuracy of HCP5 was verified by agarose gel electrophoresis (AGE) and Sanger sequencing. Simultaneously, the expression level of serum HCP5 was detected by qRT-PCR in 98 patients with primary gastric cancer, 21 gastritis patients, 82 healthy donors, and multiple cancer types. Then, the methodology analysis was carried on. Moreover, receiver operating characteristic (ROC) was used to evaluate its diagnostic efficiency. RESULTS: qRT-PCR method had good repeatability and stability in detecting HCP5. The expression level of HCP5 in the serum of gastric cancer patients was remarkably higher than that of healthy controls, and it could distinguish gastritis patients from healthy donors. Besides, the expression of HCP5 was increased dramatically in MKN-45 and MGC-803. The FISH assay showed that HCP5 was mainly distributed in the cytoplasm of MKN-45 and BGC-823 cells. When HCP5 was combined with existing tumor markers, the diagnostic efficiency of HCP5 was the best, and the combined diagnosis of carcinoembryonic antigen (CEA), carbohydrate antigen199 (CA199), and HCP5 can significantly improve the diagnostic sensitivity. Besides, compared with the expression levels of thyroid cancer (THCA), colorectal cancer (CRC), and breast cancer (BRCA), serum HCP5 in gastric cancer was the most specific. Moreover, the high expression of serum HCP5 was related to differentiation, lymph node metastasis, and nerve invasion. The term of serum HCP5 after the operation was significantly lower than that of patients with primary gastric cancer. CONCLUSION: Serum HCP5 can be used as a potential biomarker of non-invasive fluid biopsy, which had a unique value in the early diagnosis, development, and prognosis of gastric cancer. Frontiers Media S.A. 2021-06-18 /pmc/articles/PMC8252797/ /pubmed/34222007 http://dx.doi.org/10.3389/fonc.2021.684531 Text en Copyright © 2021 Qin, Yang, Kong, Xu, Liang and Ju https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Qin, Shiyi
Yang, Lei
Kong, Shan
Xu, Yanhua
Liang, Bo
Ju, Shaoqing
LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer
title LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer
title_full LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer
title_fullStr LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer
title_full_unstemmed LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer
title_short LncRNA HCP5 : A Potential Biomarker for Diagnosing Gastric Cancer
title_sort lncrna hcp5 : a potential biomarker for diagnosing gastric cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252797/
https://www.ncbi.nlm.nih.gov/pubmed/34222007
http://dx.doi.org/10.3389/fonc.2021.684531
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