However counterintuitive, the association between saliva and the dental environment AND pancreatic cancer (ductal adenocarcinoma of the pancreas) continues to garner highly interesting research. One team lead by David T. Wong and colleagues at the Dental Research Institute of the UCLA School of Dentistry in Los Angeles, California first came to our attention per the Pancreatica blog on 6/23 of this year for a 2010 article in the journal Gastroenterology laying the basis for salivary biomarkers for cancer of the pancreas, and later for a 2012 article in the journal Gut postulating specific oral bacteria as associated with pancreatic cancer.
This UCLA team has now published an article in the September 13, 2013 issue of the Journal of Biological Chemistry that lays an intriguing and perhaps even likely possible predicate for the mechanism by which salivary fluid may be specifically affected by such apparently distal and unrelated diseases such as pancreatic cancer.
Before presenting the results of their research, we should discuss the concept of exosomes. Identified in the late 1980s, these are tiny (30 to 100 nanometers in diameter) durable vesicles or bubble-like structures that are found in most biological fluids. They have been found to contain proteins and other substances including messenger-RNA. In an over-simplistic statement, these structures appear to facilitate or at least affect such processes such as cell-to-cell communication throughout the body, coagulation, waste management, tumor invasion, and the immune response. The origin of exosomes is from within cells – and then in some cases, the plasma cell wall releases an exosome to extracellular space within which it can travel.
Wong and his fellow researchers in this present work, studied the role of exosomes that derived from pancreatic cancer tissue – and evaluated their presence and possible function in saliva in a mouse model. They developed a mouse that gave specific biomarkers for pancreatic cancer by implanting a pancreatic cancer cell line into the animal’s pancreas – and then identifying a selective panel of biomarkers and thereupon testing for these markers in the saliva of those mice with pancreatic cancer (which were found) as compared to those without (not found). Almost all of the components of this panel of seven gene-derived transcriptomic biomarkers were found in the affected mice tumor, serum, saliva, and exosomes.
Then the researchers used a modified tumor line that tended to suppress exosome production from the pancreatic cancer tissue. They then again looked at these mice tissues and found that almost none of the components of the seven biomarker panel were found in the saliva of these affected mice. This allowed the researchers to cautiously postulate a working theory that tumor-derived exosomes may be central to the pathway that establishes salivary biomarkers that appear to be specific for (in this case) pancreatic cancer. The authors call for further research to more fully explicate the precise course of the pathways in this process.
And we could ask for nothing more as a follow-on to this growing body of evidence from this clearly talented research team.
Dale O’Brien, MD