Imperial College London

DrLeandroCastellano

Faculty of MedicineDepartment of Surgery & Cancer

Visiting Reader
 
 
 
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Contact

 

+44 (0)20 7594 2822l.castellano Website

 
 
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Location

 

ICTEM buildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Frampton:2018:10.18632/oncotarget.24873,
author = {Frampton, AE and Mato, Prado M and Lopez, Jimenez ME and Fajardo, Puerta AB and Jawad, ZR and Lawton, P and Giovannetti, E and Habib, N and Castellano, L and Stebbing, J and Krell, J and Jiao, L},
doi = {10.18632/oncotarget.24873},
journal = {Oncotarget},
pages = {19006--19013},
title = {Glypican-1 is enriched in circulating-exosomes in pancreatic cancer and correlates with tumor burden},
url = {http://dx.doi.org/10.18632/oncotarget.24873},
volume = {9},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Background: Glypican-1 (GPC1) is expressed in pancreatic ductal adenocarcinoma (PDAC) cells and adjacent stroma fibroblasts. Recently, GPC1 circulating exosomes (crExos) have been shown to be able to detect early stages of PDAC. This study investigated the usefulness of crExos GPC1 as a biomarker for PDAC.Methods: Plasma was obtained from patients with benign pancreatic disease (n = 16) and PDAC (n = 27) prior to pancreatectomy, and crExos were isolated by ultra-centrifugation. Protein was extracted from surgical specimens (adjacent normal pancreas, n = 13; and PDAC, n = 17). GPC1 levels were measured using enzyme-linked immunosorbent assay (ELISA). Results: There was no significant difference in GPC1 levels between normal pancreas and PDAC tissues. This was also true when comparing matched pairs. However, GPC1 levels were enriched in PDAC crExos (n = 11), compared to the source tumors (n = 11; 97 ± 54 vs. 20.9 ± 12.3 pg/mL; P < 0.001). In addition, PDACs with high GPC1 expression tended to have crExos with high GPC1 levels. Despite these findings, we were unable to distinguish PDAC from benign pancreatic disease using crExos GPC1 levels. Interestingly, we found that in matched pre and post-operative plasma samples there was a significant drop in crExos GPC1 levels after surgical resection for PDAC (n = 11 vs. 11; 97 ± 54 vs. 77.8 ± 32.4 pg/mL; P = 0.0428). Furthermore, we found that patients with high crExos GPC1 levels have significantly larger PDACs (>4 cm; P = 0.012). Conclusions: High GPC1 crExos may be able to determine PDAC tumor size and disease burden. However, further efforts are needed to elucidate its role as a diagnostic and/or prognostic biomarker using larger cohorts of PDAC patients.
AU - Frampton,AE
AU - Mato,Prado M
AU - Lopez,Jimenez ME
AU - Fajardo,Puerta AB
AU - Jawad,ZR
AU - Lawton,P
AU - Giovannetti,E
AU - Habib,N
AU - Castellano,L
AU - Stebbing,J
AU - Krell,J
AU - Jiao,L
DO - 10.18632/oncotarget.24873
EP - 19013
PY - 2018///
SN - 1949-2553
SP - 19006
TI - Glypican-1 is enriched in circulating-exosomes in pancreatic cancer and correlates with tumor burden
T2 - Oncotarget
UR - http://dx.doi.org/10.18632/oncotarget.24873
UR - http://hdl.handle.net/10044/1/57827
VL - 9
ER -