Evidence map›Paper›PMID 31323382›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2020

Methylated DNA in Pancreatic Juice Distinguishes Patients With Pancreatic Cancer From Controls.

Shounak Majumder, Massimo Raimondo, William R Taylor, Tracy C Yab, Calise K Berger, Brian A Dukek, Xiaoming Cao, Patrick H Foote, Chung Wah Wu, Mary E Devens and 20 more

Open access · greenAbstract read
In one paragraph

Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Organoid technology in cancer research.Molecular biomedicine · 2026
    Review
  4. Review
  5. Strategy for early diagnosis of pancreatic cancer.Frontiers in gastroenterology (Lausanne, Switzerland) · 2026
    Review
  6. Article
  7. Multimodal Pancreatic Cancer Detection Using Methylated DNA Biomarkers in Pancreatic Juice and Plasma CA 19-9: A Prospective Multicenter Study.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Role of ELMO1 in inflammation and cancer-clinical implications.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review
  16. Article
  17. Review
  18. The expression of mGland surgery · 2022
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 5 institutions in 1 country.

Shounak MajumderDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. Electronic address: majumder.shounak@mayo.edu.
Massimo RaimondoDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida.
William R TaylorDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Tracy C YabDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Calise K BergerDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Brian A DukekDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Xiaoming CaoDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Patrick H FooteDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Chung Wah WuDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Mary E DevensDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Douglas W MahoneyDepartment of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.
Thomas C SmyrkDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Rahul PannalaDivision of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona.
Suresh T ChariDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Santhi Swaroop VegeDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Mark D TopazianDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Bret T PetersenDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Michael J LevyDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Elizabeth RajanDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Ferga C GleesonDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Barham Abu DayyehDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Cuong C NguyenDivision of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona.
Douglas O FaigelDivision of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona.
Timothy A WoodwardDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida.
Michael B WallaceDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida.
Gloria PetersenDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Hatim T AllawiExact Sciences Corporation, Madison, Wisconsin.
Graham P LidgardExact Sciences Corporation, Madison, Wisconsin.
John B KisielDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
David A AhlquistDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Mayo Clinic · USJacksonville College · USMayo Clinic in Arizona · USExact Sciences (United States) · USMayo Clinic in Florida · US

Funding

Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI MUKHOPADHYAY, DEBABRATA · 2004 to 2018
$32.7M
Mayo Clinic Prospective Resource for Biomarker Validation and Early Detection of Pancreatic CancerU01CA210138 · NCI · MAYO CLINIC ROCHESTER · PI Shounak Majumder, Kenneth Zaret · 2016 to 2026
$9.0M
Multi-site Gastrointestinal Cancer Detection by Stool DNA MethylationR37CA214679 · NCI · MAYO CLINIC ROCHESTER · PI KISIEL, JOHN · 2018 to 2024
$2.8M
Multi-cancer Early DetectionR01CA214679 · NCI · MAYO CLINIC ROCHESTER · PI John Kisiel, Niloy Jewel Samadder · 2025 to 2026
$891k
NCI NIH HHS P50 CA102701NCI NIH HHS R01 CA214679NCI NIH HHS R37 CA214679NCI NIH HHS U01 CA210138
6 · The paper itself

Abstract

BACKGROUND &

aimsPrecursors of pancreatic cancer arise in the ductal epithelium; markers exfoliated into pancreatic juice might be used to detect high-grade dysplasia (HGD) and cancer. Specific methylated DNA sequences in pancreatic tissue have been associated with adenocarcinoma. We analyzed these methylated DNA markers (MDMs) in pancreatic juice samples from patients with pancreatic ductal adenocarcinomas (PDACs) or intraductal papillary mucinous neoplasms (IPMNs) with HGD (cases), and assessed their ability to discriminate these patients from individuals without dysplasia or with IPMNs with low-grade dysplasia (controls).

methodsWe obtained pancreatic juice samples from 38 patients (35 with biopsy-proven PDAC or pancreatic cystic lesions with invasive cancer and 3 with HGD) and 73 controls (32 with normal pancreas and 41 with benign disease), collected endoscopically from the duodenum after secretin administration from February 2015 through November 2016 at 3 medical centers. Samples were analyzed for the presence of 14 MDMs (in the genes NDRG4, BMP3, TBX15, C13orf18, PRKCB, CLEC11A, CD1D, ELMO1, IGF2BP1, RYR2, ADCY1, FER1L4, EMX1, and LRRC4), by quantitative allele-specific real-time target and signal amplification. We performed area under the receiver operating characteristic curve analyses to determine the ability of each marker, and panels of markers, to distinguish patients with HGD and cancer from controls. MDMs were combined to form a panel for detection using recursive partition trees.

resultsWe identified a group of 3 MDMs (at C13orf18, FER1L4, and BMP3) in pancreatic juice that distinguished cases from controls with an area under the receiver operating characteristic value of 0.90 (95% CI, 0.83-0.97). Using a specificity cut-off value of 86%, this group of MDMs distinguished patients with any stage of pancreatic cancer from controls with 83% sensitivity (95% CI, 66%-93%) and identified patients with stage I or II PDAC or IPMN with HGD with 80% sensitivity (95% CI, 56%-95%).

conclusionsWe identified a group of 3 MDMs in pancreatic juice that identify patients with pancreatic cancer with an area under the receiver operating characteristic value of 0.90, including patients with early stage disease or advanced precancer. These DNA methylation patterns might be included in algorithms for early detection of pancreatic cancer, especially in high-risk cohorts. Further optimization and clinical studies are needed.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsDNAEarly Detection of CancerHumansPancreatic JuiceDNAChemistryNeoplasmPrognosticSecretin

Identifiers

PMID31323382
PMCPMC6984349
OpenAlexW2957825377

What OpenQuestion holds

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LicenceTDM
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Registered trials

None linked

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.