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Circulating Tissue Polypeptide-Specific Antigen in Pre-Diagnostic Pancreatic Cancer Samples
Emmy Borgmästars1, Erik Lundberg1, Daniel Öhlund2,3
1Department of Surgical and Perioperative Sciences/Surgery, Umeå University, 901 85 Umeå, Sweden.
Cancers
|November 13, 2021
Summary
Tissue polypeptide specific antigen (TPS) does not show potential for early pancreatic ductal adenocarcinoma (PDAC) detection. TPS levels were low in pre-diagnostic samples but significantly increased at PDAC diagnosis, indicating late-stage changes.
Area of Science:
- Oncology
- Biomarker Discovery
- Gastroenterology
Background:
- Early detection of pancreatic ductal adenocarcinoma (PDAC) is critical for improving patient survival rates.
- Current biomarkers, like carbohydrate antigen 19-9 (CA 19-9), have limitations in early PDAC diagnosis.
- Tissue polypeptide specific antigen (TPS) has been investigated as a potential alternative biomarker.
Purpose of the Study:
- To evaluate the potential of Tissue polypeptide specific antigen (TPS) as an early detection biomarker for pancreatic ductal adenocarcinoma (PDAC).
- To compare TPS levels in pre-diagnostic plasma samples with those from healthy controls and at the time of PDAC diagnosis.
Main Methods:
- A case-control study utilizing pre-diagnostic plasma samples from 267 future PDAC patients and 320 matched healthy controls.
- Enzyme-linked immunosorbent assay (ELISA) was used to measure plasma TPS levels.
- Longitudinal analysis was performed on a subset of individuals with multiple pre-diagnostic samples.
Main Results:
- Circulating TPS levels were low in both pre-diagnostic PDAC samples and healthy controls.
- TPS levels were significantly increased at the time of PDAC diagnosis compared to pre-diagnostic samples.
- Logistic regression analysis adjusted for age showed a significant increase in TPS at diagnosis (OR 1.03; 95% CI: 1.01-1.05).
Conclusions:
- Tissue polypeptide specific antigen (TPS) levels rise late in the progression of pancreatic ductal adenocarcinoma (PDAC).
- TPS does not demonstrate potential as a biomarker for the early detection of PDAC.
- Further research may be needed to explore other biomarkers for early PDAC diagnosis.

