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Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma

Diagnostic and/or prognostic biomarkers for cholangiocarcinoma (CCA) are still insufficient with poor prognosis of patients. To discover a new CCA biomarker, we constructed our secretome database of three CCA cell lines and one control cholangiocyte cell line using GeLC-MS/MS. We selected candidate...

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Autores principales: Tummanatsakun, Doungdean, Proungvitaya, Tanakorn, Roytrakul, Sittiruk, Limpaiboon, Temduang, Wongkham, Sopit, Wongkham, Chaisiri, Silsirivanit, Atit, Somintara, Ongart, Sangkhamanon, Sakkarn, Proungvitaya, Siriporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770206/
https://www.ncbi.nlm.nih.gov/pubmed/31454981
http://dx.doi.org/10.3390/biom9090413
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author Tummanatsakun, Doungdean
Proungvitaya, Tanakorn
Roytrakul, Sittiruk
Limpaiboon, Temduang
Wongkham, Sopit
Wongkham, Chaisiri
Silsirivanit, Atit
Somintara, Ongart
Sangkhamanon, Sakkarn
Proungvitaya, Siriporn
author_facet Tummanatsakun, Doungdean
Proungvitaya, Tanakorn
Roytrakul, Sittiruk
Limpaiboon, Temduang
Wongkham, Sopit
Wongkham, Chaisiri
Silsirivanit, Atit
Somintara, Ongart
Sangkhamanon, Sakkarn
Proungvitaya, Siriporn
author_sort Tummanatsakun, Doungdean
collection PubMed
description Diagnostic and/or prognostic biomarkers for cholangiocarcinoma (CCA) are still insufficient with poor prognosis of patients. To discover a new CCA biomarker, we constructed our secretome database of three CCA cell lines and one control cholangiocyte cell line using GeLC-MS/MS. We selected candidate proteins by five bioinformatics tools for secretome analysis. The inclusion criteria were as follows: having predicted signal peptide or being predicted as non-classically secreted protein; together with having no transmembrane helix and being previously detected in plasma and having the highest number of signal peptide cleavage sites. Eventually, apurinic/apyrimidinic endodeoxyribonuclease 1 (APEX1) was selected for further analysis. To validate APEX1 as a bio-marker for CCA, serum APEX1 levels of 80, 39, and 40 samples collected from CCA, benign biliary diseases (BBD), and healthy control groups, respectively, were measured using dot blot analysis. The results showed that serum APEX1 level in CCA group was significantly higher than that in BBD or healthy control group. Among CCA patients, serum APEX1 level was significantly higher in patients having metastasis than in those without metastasis. The higher level of serum APEX1 was correlated with the shorter survival time of the patients. Serum APEX1 level might be a diagnostic and prognostic biomarker for CCA.
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spelling pubmed-67702062019-10-30 Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma Tummanatsakun, Doungdean Proungvitaya, Tanakorn Roytrakul, Sittiruk Limpaiboon, Temduang Wongkham, Sopit Wongkham, Chaisiri Silsirivanit, Atit Somintara, Ongart Sangkhamanon, Sakkarn Proungvitaya, Siriporn Biomolecules Article Diagnostic and/or prognostic biomarkers for cholangiocarcinoma (CCA) are still insufficient with poor prognosis of patients. To discover a new CCA biomarker, we constructed our secretome database of three CCA cell lines and one control cholangiocyte cell line using GeLC-MS/MS. We selected candidate proteins by five bioinformatics tools for secretome analysis. The inclusion criteria were as follows: having predicted signal peptide or being predicted as non-classically secreted protein; together with having no transmembrane helix and being previously detected in plasma and having the highest number of signal peptide cleavage sites. Eventually, apurinic/apyrimidinic endodeoxyribonuclease 1 (APEX1) was selected for further analysis. To validate APEX1 as a bio-marker for CCA, serum APEX1 levels of 80, 39, and 40 samples collected from CCA, benign biliary diseases (BBD), and healthy control groups, respectively, were measured using dot blot analysis. The results showed that serum APEX1 level in CCA group was significantly higher than that in BBD or healthy control group. Among CCA patients, serum APEX1 level was significantly higher in patients having metastasis than in those without metastasis. The higher level of serum APEX1 was correlated with the shorter survival time of the patients. Serum APEX1 level might be a diagnostic and prognostic biomarker for CCA. MDPI 2019-08-26 /pmc/articles/PMC6770206/ /pubmed/31454981 http://dx.doi.org/10.3390/biom9090413 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tummanatsakun, Doungdean
Proungvitaya, Tanakorn
Roytrakul, Sittiruk
Limpaiboon, Temduang
Wongkham, Sopit
Wongkham, Chaisiri
Silsirivanit, Atit
Somintara, Ongart
Sangkhamanon, Sakkarn
Proungvitaya, Siriporn
Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma
title Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma
title_full Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma
title_fullStr Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma
title_full_unstemmed Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma
title_short Serum Apurinic/Apyrimidinic Endodeoxyribonuclease 1 (APEX1) Level as a Potential Biomarker of Cholangiocarcinoma
title_sort serum apurinic/apyrimidinic endodeoxyribonuclease 1 (apex1) level as a potential biomarker of cholangiocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770206/
https://www.ncbi.nlm.nih.gov/pubmed/31454981
http://dx.doi.org/10.3390/biom9090413
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