Role of Pancreatic Cancer-derived Exosomes in Salivary Biomarker Development
Open accessAbstract
Recent studies have demonstrated that discriminatory salivary biomarkers can be readily detected upon the development of systemic diseases such as pancreatic cancer, breast cancer, lung cancer, and ovarian cancer. However, the utility of salivary biomarkers for the detection of systemic diseases has been undermined due to the absence of the biological and mechanistic rationale as to why distal diseases from the oral cavity would lead to the development of discriminatory biomarkers in saliva. Here, we examine the hypothesis that pancreatic tumor-derived exosomes are mechanistically involved in the development of pancreatic cancer-discriminatory salivary transcriptomic biomarkers. We first developed a pancreatic cancer mouse model that yielded discriminatory salivary biomarkers by implanting the mouse pancreatic cancer cell line Panc02 into the pancreas of the syngeneic host C57BL/6. The role of pancreatic cancer-derived exosomes in the development of discriminatory salivary biomarkers was then tested by engineering a Panc02 cell line that is suppressed for exosome biogenesis, implanting into the C56BL/6 mouse, and examining whether the discriminatory salivary biomarker profile was ablated or disrupted. Suppression of exosome biogenesis results in the ablation of discriminatory salivary biomarker development. This study supports that tumor-derived exosomes provide a mechanism in the development of discriminatory biomarkers in saliva and distal systemic diseases. Background: Salivary biomarkers for systemic diseases have been undermined due to lack of mechanistic and biological rationale. Results: Suppression of exosome biogenesis leads to ablation of salivary biomarkers. Conclusion: Tumor-derived exosomes provide a mechanism for discriminatory biomarkers in saliva. Significance: Tumor-derived exosomes provide the scientific rationale that connects pancreatic tumors and the oral cavity leading to salivary biomarkers.
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Blood remains the most commonly studied biospecimen for early detection, but many analytes are also present in other proximate samples, including pancreatic juice, stool, urine, saliva, and pancreatic cyst fluid.
“In passing, it also needs to be stated that, although blood remains the most commonly studied biospecimen for early detection, many of the analytes are also present in other proximate samples, including pancreatic juice,53,54 stool,55 urine,56,57 saliva,58 and pancreatic cyst fluid.59”
From Artificial Intelligence and Early Detection of Pancreatic Cancer: 2020 Summative Review (2021) · cites this paper as [58]
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Artificial Intelligence and Early Detection of Pancreatic Cancer: 2020 Summative Review
Kenner, B., Chari, S. T., Kelsen, D., Klimstra, D. S., Pandol, S. J., Rosenthal, M., Rustgi, A. K., Taylor, J. A., Yala, A., Abul-Husn, N., et al. (2021) · Pancreas · doi:10.1097/mpa.0000000000001762 · Cited by 158 · see citing works
Biomarkers for early diagnosis of pancreatic cancer
Jenkinson, C., Earl, J., Ghaneh, P., Halloran, C., Carrato, A., Greenhalf, W., Neoptolemos, J., & Costello, E. (2015) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/17474124.2015.965145 · Cited by 42 · see citing works
- Authors
- Lau, C., Kim, Y., Chia, D., Spielmann, N., Eibl, G., Elashoff, D., Wei, F., Lin, Y.-L., Moro, A., Grogan, T., Chiang, S., Feinstein, E., Schafer, C., Farrell, J., & Wong, D. T. W.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Wong, David T.W.
- ORCID
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2013-09
- Volume
- 288
- Issue
- 37
- Pages
- 26888-26897
- ISSN
- 0021-9258 (ISSN-L)
- PMC
- PMC3772238
- OpenAlex
- W2131085014
- Cited by
- 256
- References
- 0
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 13 · 2023: 14 · 2022: 22 · 2021: 25 · 2020: 22 · 2019: 25 · 2018: 25 · 2017: 25 · 2016: 17 · 2015: 28 · 2014: 19 · 2013: 1
- FWCI
- 9.71
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institutes of Health (UL1TR000124, UH3TR000923, UH2TR000923)
- National Cancer Institute (R01CA122042)
- National Institute of Dental and Craniofacial Research (T32 DE07296, R01-DE17170, R01DE017170, T90DE022734, T32DE007296)
- National Center for Advancing Translational Sciences (UH2/UH3 TR000923)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Health Sciences › Medicine › Physiology › Salivary Gland Disorders and Functions
- Health Sciences › Medicine › Surgery › Salivary Gland Tumors Diagnosis and Treatment
- Keywords
- pancreatic cancer, exosomes, salivary biomarkers, exosome biogenesis, tumor-derived exosomes, systemic disease detection, oral cavity
- MeSH terms
- Acetylcholine, Animals, Esterases, Humans, Mice, Inbred C57BL, Neoplasm Transplantation, Pancreas, Pancreatic Neoplasms, Saliva, Biomarkers, Tumor, Gene Expression Regulation, Neoplastic, Oligonucleotide Array Sequence Analysis, Cell Line, Tumor, Microscopy, Electron, Transmission, Mice, Exosomes, Transcriptome
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