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Measurement of serum PODXL concentration for detection of pancreatic cancer

BACKGROUND: The aim of this study was to investigate the use of podocalyxin (PODXL) and secretoglobin family 1D, member 2 (SCGB1D2) expressions in whole blood as diagnostic biomarkers to distinguish between patients with pancreatic cancer and control participants, in comparison with serum cancer ant...

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Autores principales: Taniuchi, Keisuke, Tsuboi, Makiko, Sakaguchi, Masahiko, Saibara, Toshiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858829/
https://www.ncbi.nlm.nih.gov/pubmed/29588598
http://dx.doi.org/10.2147/OTT.S155367
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author Taniuchi, Keisuke
Tsuboi, Makiko
Sakaguchi, Masahiko
Saibara, Toshiji
author_facet Taniuchi, Keisuke
Tsuboi, Makiko
Sakaguchi, Masahiko
Saibara, Toshiji
author_sort Taniuchi, Keisuke
collection PubMed
description BACKGROUND: The aim of this study was to investigate the use of podocalyxin (PODXL) and secretoglobin family 1D, member 2 (SCGB1D2) expressions in whole blood as diagnostic biomarkers to distinguish between patients with pancreatic cancer and control participants, in comparison with serum cancer antigen 19-9 (CA19-9), which is the current clinical standard. PATIENTS AND METHODS: Flow cytometric analysis was performed to determine the expressions of PODXL and SCGB1D2 on the surface of cultured pancreatic cancer cells. Immunoblotting was performed to determine whether PODXL and SCGB1D2 were detectable in the media of cultured pancreatic cancer cells. A discovery-stage clinical study was performed in a cohort of 23 patients with pancreatic cancer and 51 control individuals without pancreatic disease who had been treated in the Department of Gastroenterology and Hepatology at Kochi Medical School Hospital from April 2014 to January 2016. Serum PODXL and SCGB1D2 levels were measured by enzyme-linked immunosorbent assay (ELISA). RESULTS: PODXL and SCGB1D2 accumulated in the protrusions of cultured pancreatic cancer cells, and they were detectable both on the cell surface and in the cultured media from these cells. The discovery-stage clinical study showed that the area under the receiver-operating characteristic curve (AUC) was 0.96 (95% confidence interval [CI] 0.91–1.000) for PODXL, 0.80 (95% CI 0.67–0.94) for SCGB1D2, and 0.78 (95% CI 0.66–0.90) for CA19-9. The AUC for PODXL was thus significantly higher than that for CA19-9 (P = 0.006). The combination of SCGB1D2 with CA19-9 did not significantly increase the AUC (0.83; 95% CI 0.70–0.96) compared with the AUC for either SCGB1D2 or CA19-9 alone (P = 0.563). CONCLUSION: PODXL may be a novel, non-invasive diagnostic biomarker for the detection of pancreatic cancer.
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spelling pubmed-58588292018-03-27 Measurement of serum PODXL concentration for detection of pancreatic cancer Taniuchi, Keisuke Tsuboi, Makiko Sakaguchi, Masahiko Saibara, Toshiji Onco Targets Ther Original Research BACKGROUND: The aim of this study was to investigate the use of podocalyxin (PODXL) and secretoglobin family 1D, member 2 (SCGB1D2) expressions in whole blood as diagnostic biomarkers to distinguish between patients with pancreatic cancer and control participants, in comparison with serum cancer antigen 19-9 (CA19-9), which is the current clinical standard. PATIENTS AND METHODS: Flow cytometric analysis was performed to determine the expressions of PODXL and SCGB1D2 on the surface of cultured pancreatic cancer cells. Immunoblotting was performed to determine whether PODXL and SCGB1D2 were detectable in the media of cultured pancreatic cancer cells. A discovery-stage clinical study was performed in a cohort of 23 patients with pancreatic cancer and 51 control individuals without pancreatic disease who had been treated in the Department of Gastroenterology and Hepatology at Kochi Medical School Hospital from April 2014 to January 2016. Serum PODXL and SCGB1D2 levels were measured by enzyme-linked immunosorbent assay (ELISA). RESULTS: PODXL and SCGB1D2 accumulated in the protrusions of cultured pancreatic cancer cells, and they were detectable both on the cell surface and in the cultured media from these cells. The discovery-stage clinical study showed that the area under the receiver-operating characteristic curve (AUC) was 0.96 (95% confidence interval [CI] 0.91–1.000) for PODXL, 0.80 (95% CI 0.67–0.94) for SCGB1D2, and 0.78 (95% CI 0.66–0.90) for CA19-9. The AUC for PODXL was thus significantly higher than that for CA19-9 (P = 0.006). The combination of SCGB1D2 with CA19-9 did not significantly increase the AUC (0.83; 95% CI 0.70–0.96) compared with the AUC for either SCGB1D2 or CA19-9 alone (P = 0.563). CONCLUSION: PODXL may be a novel, non-invasive diagnostic biomarker for the detection of pancreatic cancer. Dove Medical Press 2018-03-15 /pmc/articles/PMC5858829/ /pubmed/29588598 http://dx.doi.org/10.2147/OTT.S155367 Text en © 2018 Taniuchi et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Taniuchi, Keisuke
Tsuboi, Makiko
Sakaguchi, Masahiko
Saibara, Toshiji
Measurement of serum PODXL concentration for detection of pancreatic cancer
title Measurement of serum PODXL concentration for detection of pancreatic cancer
title_full Measurement of serum PODXL concentration for detection of pancreatic cancer
title_fullStr Measurement of serum PODXL concentration for detection of pancreatic cancer
title_full_unstemmed Measurement of serum PODXL concentration for detection of pancreatic cancer
title_short Measurement of serum PODXL concentration for detection of pancreatic cancer
title_sort measurement of serum podxl concentration for detection of pancreatic cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858829/
https://www.ncbi.nlm.nih.gov/pubmed/29588598
http://dx.doi.org/10.2147/OTT.S155367
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