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Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection

BACKGROUND: To discover novel markers for improving the efficacy of pancreatic cancer (PC) diagnosis, the secretome of two PC cell lines (BxPC-3 and MIA PaCa-2) was profiled. UL16 binding protein 2 (ULBP2), one of the proteins identified in the PC cell secretome, was selected for evaluation as a bio...

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Autores principales: Chang, Ya-Ting, Wu, Chih-Ching, Shyr, Yi-Ming, Chen, Tse-Ching, Hwang, Tsann-Long, Yeh, Ta-Sen, Chang, Kai-Ping, Liu, Hao-Ping, Liu, Yu-Ling, Tsai, Ming-Hung, Chang, Yu-Sun, Yu, Jau-Song
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098863/
https://www.ncbi.nlm.nih.gov/pubmed/21625447
http://dx.doi.org/10.1371/journal.pone.0020029
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author Chang, Ya-Ting
Wu, Chih-Ching
Shyr, Yi-Ming
Chen, Tse-Ching
Hwang, Tsann-Long
Yeh, Ta-Sen
Chang, Kai-Ping
Liu, Hao-Ping
Liu, Yu-Ling
Tsai, Ming-Hung
Chang, Yu-Sun
Yu, Jau-Song
author_facet Chang, Ya-Ting
Wu, Chih-Ching
Shyr, Yi-Ming
Chen, Tse-Ching
Hwang, Tsann-Long
Yeh, Ta-Sen
Chang, Kai-Ping
Liu, Hao-Ping
Liu, Yu-Ling
Tsai, Ming-Hung
Chang, Yu-Sun
Yu, Jau-Song
author_sort Chang, Ya-Ting
collection PubMed
description BACKGROUND: To discover novel markers for improving the efficacy of pancreatic cancer (PC) diagnosis, the secretome of two PC cell lines (BxPC-3 and MIA PaCa-2) was profiled. UL16 binding protein 2 (ULBP2), one of the proteins identified in the PC cell secretome, was selected for evaluation as a biomarker for PC detection because its mRNA level was also found to be significantly elevated in PC tissues. METHODS: ULBP2 expression in PC tissues from 67 patients was studied by immunohistochemistry. ULBP2 serum levels in 154 PC patients and 142 healthy controls were measured by bead-based immunoassay, and the efficacy of serum ULBP2 for PC detection was compared with the widely used serological PC marker carbohydrate antigen 19-9 (CA 19-9). RESULTS: Immunohistochemical analyses revealed an elevated expression of ULPB2 in PC tissues compared with adjacent non-cancerous tissues. Meanwhile, the serum levels of ULBP2 among all PC patients (n = 154) and in early-stage cancer patients were significantly higher than those in healthy controls (p<0.0001). The combination of ULBP2 and CA 19-9 outperformed each marker alone in distinguishing PC patients from healthy individuals. Importantly, an analysis of the area under receiver operating characteristic curves showed that ULBP2 was superior to CA 19-9 in discriminating patients with early-stage PC from healthy controls. CONCLUSIONS: Collectively, our results indicate that ULBP2 may represent a novel and useful serum biomarker for pancreatic cancer primary screening.
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spelling pubmed-30988632011-05-27 Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection Chang, Ya-Ting Wu, Chih-Ching Shyr, Yi-Ming Chen, Tse-Ching Hwang, Tsann-Long Yeh, Ta-Sen Chang, Kai-Ping Liu, Hao-Ping Liu, Yu-Ling Tsai, Ming-Hung Chang, Yu-Sun Yu, Jau-Song PLoS One Research Article BACKGROUND: To discover novel markers for improving the efficacy of pancreatic cancer (PC) diagnosis, the secretome of two PC cell lines (BxPC-3 and MIA PaCa-2) was profiled. UL16 binding protein 2 (ULBP2), one of the proteins identified in the PC cell secretome, was selected for evaluation as a biomarker for PC detection because its mRNA level was also found to be significantly elevated in PC tissues. METHODS: ULBP2 expression in PC tissues from 67 patients was studied by immunohistochemistry. ULBP2 serum levels in 154 PC patients and 142 healthy controls were measured by bead-based immunoassay, and the efficacy of serum ULBP2 for PC detection was compared with the widely used serological PC marker carbohydrate antigen 19-9 (CA 19-9). RESULTS: Immunohistochemical analyses revealed an elevated expression of ULPB2 in PC tissues compared with adjacent non-cancerous tissues. Meanwhile, the serum levels of ULBP2 among all PC patients (n = 154) and in early-stage cancer patients were significantly higher than those in healthy controls (p<0.0001). The combination of ULBP2 and CA 19-9 outperformed each marker alone in distinguishing PC patients from healthy individuals. Importantly, an analysis of the area under receiver operating characteristic curves showed that ULBP2 was superior to CA 19-9 in discriminating patients with early-stage PC from healthy controls. CONCLUSIONS: Collectively, our results indicate that ULBP2 may represent a novel and useful serum biomarker for pancreatic cancer primary screening. Public Library of Science 2011-05-20 /pmc/articles/PMC3098863/ /pubmed/21625447 http://dx.doi.org/10.1371/journal.pone.0020029 Text en Chang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chang, Ya-Ting
Wu, Chih-Ching
Shyr, Yi-Ming
Chen, Tse-Ching
Hwang, Tsann-Long
Yeh, Ta-Sen
Chang, Kai-Ping
Liu, Hao-Ping
Liu, Yu-Ling
Tsai, Ming-Hung
Chang, Yu-Sun
Yu, Jau-Song
Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection
title Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection
title_full Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection
title_fullStr Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection
title_full_unstemmed Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection
title_short Secretome-Based Identification of ULBP2 as a Novel Serum Marker for Pancreatic Cancer Detection
title_sort secretome-based identification of ulbp2 as a novel serum marker for pancreatic cancer detection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098863/
https://www.ncbi.nlm.nih.gov/pubmed/21625447
http://dx.doi.org/10.1371/journal.pone.0020029
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