DNA Hypomethylation in Pancreatic Cancer Tissues Before Treatment, Defined by KRAS -mutated Circulating Tumor DNA, is Associated With Poor Prognosis.

OBJECTIVES

Aberrant hypomethylation of long interspersed nucleotide element-1 (LINE-1) and satellite alpha (SATa) in pancreatic cancer cells increases malignant potential. In addition, circulating tumor DNA (ctDNA) is likely to be associated with micrometastasis and appears more frequently in advanced pancreatic ductal adenocarcinoma (PDAC) patients. In this study, we elucidated the relationship between these factors.

MATERIALS AND

METHODS

A total of 37 patients with PDAC who underwent surgery or first-line chemotherapy were selected in 2014-2017. DNA extracted from surgical or biopsy specimens was used to calculate the relative demethylation levels (RDLs) of the LINE-1 and SATa using methylation-specific quantitative PCR. KRAS -mutated ctDNA was monitored using droplet digital PCR. Receiver operating characteristic curve analysis was performed to determine the cut-off values of LINE-1 and SATa RDLs before and after surgery or during first-line chemotherapy based on ctDNA status (presence or absence).

RESULTS

Median LINE-1 RDL before treatment was higher in patients with ctDNA than in those without, but these cut-off values (LINE-1 ≥0.058 and 0.055) peritreatments did not link to prognosis ( P =0.762 and 0.933). Conversely, the cut-off value of SATa RDL (SATa ≥0.150) based on ctDNA status after treatments showed a significant association with poor prognosis ( P =0.038). On the other hand, the cut-off value of SATa RDL (SATa ≥0.155) before treatment was found to have no association with prognosis ( P =0.408).

CONCLUSIONS

Evaluating pretreatment tumor DNA hypomethylation together with KRAS -mutated ctDNA status after surgery or initiation of first-line chemotherapy is associated with poor prognosis in PDAC.