Evidence map›Paper›PMID 35843766›Full record

ArticlePancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]2022

Tissue methylated DNA markers for sporadic pancreatic cancer are strongly associated with familial and genetically predisposed pancreatic cancer.

Shounak Majumder, William R Taylor, Patrick H Foote, Brianna J Gysbers, Xiaoming Cao, Douglas W Mahoney, Kelli N Burger, Karen A Doering, Rondell P Graham, Fergus J Couch and 2 more

Open access · greenAbstract read
In one paragraph

Article in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 55% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 2 institutions in 1 country.

Shounak MajumderDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA. Electronic address: majumder.shounak@mayo.edu.
William R TaylorDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA.
Patrick H FooteDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA.
Brianna J GysbersDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA.
Xiaoming CaoDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA.
Douglas W MahoneyDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Kelli N BurgerDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Karen A DoeringDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA.
Rondell P GrahamDivision of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
Fergus J CouchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Gloria M PetersenDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
John B KisielDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI MUKHOPADHYAY, DEBABRATA · 2004 to 2018
$32.7M
Multi-site Gastrointestinal Cancer Detection by Stool DNA MethylationR37CA214679 · NCI · MAYO CLINIC ROCHESTER · PI KISIEL, JOHN · 2018 to 2024
$2.8M
Role of Vav1 protooncogene in pancreatic cancerP20CA102701 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI PETERSEN, GLORIA M. · 2003 to 2003
$1.5M
Multi-cancer Early DetectionR01CA214679 · NCI · MAYO CLINIC ROCHESTER · PI John Kisiel, Niloy Jewel Samadder · 2025 to 2026
$891k
NCI NIH HHS P20 CA102701NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA102701NCI NIH HHS R01 CA214679NCI NIH HHS R37 CA214679
6 · The paper itself

Abstract

High-risk individuals (HRIs) with familial and genetic predisposition to pancreatic ductal adenocarcinoma (PDAC) are eligible for screening. There is no accurate biomarker for detecting early-stage PDAC. We previously demonstrated that a panel of methylated DNA markers (MDMs) accurately detect sporadic PDAC. In this study we compared the distribution of MDMs in DNA extracted from tissue of PDAC cases who carry germline mutations and non-carriers with family history, with control tissue and demonstrate high discrimination like that seen in sporadic PDAC. These results provide scientific rationale for examining plasma MDMs in HRIs with the goal of developing a minimally-invasive early detection test.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsGenetic MarkersGenetic Predisposition to DiseaseHumansGenetic MarkersBiomarkerDNA methylationPancreatic cancer

Identifiers

PMID35843766
PMCPMC9936828
OpenAlexW4283276251

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.