Evidence map›Paper›PMID 42224085›Full record

ArticlePancreas2026

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

Fumiaki Watanabe, Koichi Suzuki, Ryuji Hasebe, Yuki Mizusawa, Hidetoshi Aizawa, Iku Abe, Yuhei Endo, Kosuke Ichida, Koetsu Inoue, Hiroshi Noda and 1 more

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Article in Pancreas, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Fumiaki WatanabeDepartment of Surgery, Saitama Medical Center, Jichi Medical University, Saitama, Japan.
Koichi Suzuki
Ryuji Hasebe
Yuki Mizusawa
Hidetoshi Aizawa
Iku Abe
Yuhei Endo
Kosuke Ichida
Koetsu Inoue
Hiroshi Noda
Toshiki Rikiyama

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAberrant 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

methodsA 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).

resultsMedian 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).

conclusionsEvaluating 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.

Indexed as

Carcinoma, Pancreatic DuctalCirculating Tumor DNADNA MethylationPancreasPancreatic NeoplasmsProto-Oncogene Proteins p21(ras)AgedAntineoplastic AgentsBiomarkers, TumorEndoscopic Ultrasound-Guided Fine Needle AspirationFemaleFollow-Up StudiesHumansKaplan-Meier EstimateLong Interspersed Nucleotide ElementsMaleAntineoplastic AgentsBiomarkers, TumorCirculating Tumor DNAKRAS protein, humanProto-Oncogene Proteins p21(ras)circulating tumor DNAhypomethylationKRASlong interspersed nucleotide element 1pancreatic ductal adenocarcinomasatellite alpha

Identifiers

PMID42224085
PMCPMC13348842

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.