Microsatellite instability (MSI), resulting from inactivation of a DNA MMR gene, is more prevalent in a histologically and molecularly distinct subset of pancreatic carcinomas (28). Consistent with previous reports that the prognosis of patients with MSI positive tumors was better than that of patients with MSI negative
tumors in colorectal cancer (29), gastric cancer (30), and cancer of the papilla of Vater (31), MSI positivity in pancreatic cancer may also portend a more favorable prognosis (32). Moreover, the possibility of a germline mutation and presence of hereditary non-polyposis colorectal cancer syndrome #http://www.selleckchem.com/products/AG-014699.html keyword# (HNPCC), or Inhibitors,research,lifescience,medical Lynch syndrome, correlates with presence of defective MMR and increased susceptibility to developing other gastrointestinal malignancies. MSI-H colorectal cancers derive benefit from irinotecan therapy; whether this is also the case with pancreatic cancer remains to be determined (33). These unique molecular features of pancreatic cancer have potential utility of being developed into molecular prognostic indicators of outcome and as therapeutic targets while establishing an individualized treatment plan for a patient. These genetic abnormalities and their
Inhibitors,research,lifescience,medical incidence are represented in Table 1. At MD Anderson Cancer Center, we are investigating the role of pharmacogenetics in the individualization of therapies for pancreatic cancer. Table 1 Characteristics of prevalent genetic mutations Inhibitors,research,lifescience,medical in pancreatic adenocarcinoma Pharmacogenetics To personalize therapy, it must be recognized that considerable inter-individual variability in therapeutic outcome arises at least partly from the underling genetic profile which can impact on drug pharmacokinetics and toxicity profile (referred to as pharmacogenetics) Inhibitors,research,lifescience,medical (34). Modern technologies can allow the investigator to interrogate the pathway impacted by the study agent (candidate gene approach) or more recently, the whole genome (genome wide association studies). Implications of pharmacogenetics
are manifold and include a shift away from current paradigm of offering a standard therapy to all patients with a similar disease phenotype to an individualized treatment plan that accounts for pharmacogenetic profile. However, the ethical, legal, and economic impact resulting from rapid advances in STK38 this field is yet to be determined. Table 2 depicts previously described genetic variations of commonly used anti-cancer agents that are presently available for clinical management. Table 2 Examples of functional genetic polymorphisms and effect on chemotherapy toxicity We have investigated the variations of genes involved in the metabolism of gemcitabine, the most commonly utilized agent for pancreatic cancer.
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