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. Author manuscript; available in PMC: 2019 Oct 7.
Published in final edited form as: HPB (Oxford). 2018 Jan 12;20(7):597–604. doi: 10.1016/j.hpb.2017.12.010

Table 2.

Multiple extracellular matrix (ECM) proteins and carcinoembryonic antigen-related cell adhesion molecules (CEACAMs) were identified among the top 35 most abundant exosomal proteins from patients with PDAC compared to IPMN without microinvasive cancer and other benign diseases.

Proteins Genes PDAC (n=13) IPMNca (n=4) IPMN (n=4) Benign (n=5) p-value PDAC (LFQ*) IPMNca (LFQ*) IPMN (LFQ*) Benign (LFQ*)
Carcinoembryonic antigen-related cell adhesion molecule 1 CEACAM1 12 0 0 1 <0.001 28.7 0 0 27.2
Tenascin C TNC 11 1 0 1 0.002 28.9 29.9 0 26.5
Matrix metalloproteinase-7 MMP7 9 0 0 0 0.002 28.2 0 0 0
Laminin subunit beta-3 LAMB3 8 1 0 0 0.006 28.5 26.9 0 0
Laminin subunit gamma-2 LAMC2 8 1 0 0 0.006 29.6 28.5 0 0
Carcinoembryonic antigen-related cell adhesion molecule 5 CEACAM5 9 1 1 0 0.012 28.8 27.9 27.9 0

PDAC, pancreatic ductal adenocarcinoma; IPMN, intraductal papillary mucinous neoplasm; IPMNca, IPMN with microinvasive cancer; LFQ, label-free quantification

*

median LFQ was reported only for those present in patients of each cohort.