Evidence map›Paper›PMID 24277729›Full record

ArticleGut2014

mAb Das-1 is specific for high-risk and malignant intraductal papillary mucinous neoplasm (IPMN).

Koushik K Das, Hong Xiao, Xin Geng, Carlos Fernandez-Del-Castillo, Vicente Morales-Oyarvide, Ebubekir Daglilar, David G Forcione, Brenna C Bounds, William R Brugge, Martha B Pitman and 2 more

Open access · greenAbstract read
In one paragraph

Article in Gut, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

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  14. 3'-sulfated LewisFrontiers in cell and developmental biology · 2023
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  20. Biomarkers and Strategy to Detect Preinvasive and Early Pancreatic Cancer: State of the Field and the Impact of the EDRN.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
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 4 institutions in 1 country.

Koushik K DasDepartment of Internal Medicine, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Hong XiaoDepartment of Pathology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Xin GengDivision of Gastroenterology, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Carlos Fernandez-Del-CastilloDepartment of Surgery, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Vicente Morales-OyarvideDepartment of Pathology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA Department of Surgery, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Ebubekir DaglilarDivision of Gastroenterology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
David G ForcioneDivision of Gastroenterology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Brenna C BoundsDivision of Gastroenterology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
William R BruggeDivision of Gastroenterology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Martha B PitmanDepartment of Pathology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Mari Mino-KenudsonDepartment of Pathology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Kiron M DasDivision of Gastroenterology, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Massachusetts General Hospital · USHarvard University · USJohnson University · USRutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Tissue and Pathology ResourcesP50CA127003 · NCI · DANA-FARBER CANCER INST · PI EL-BARDEESY, NABEEL, SELLERS, WILLIAM R · 2007 to 2023
$33.2M
Studies of Esophageal Metaplasia Using a Novel AntibodyR01DK063618 · NIDDK · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI DAS, KIRON M · 2002 to 2006
$1.7M
PDG Links Stem Cell Niche to Pancreatic Epithelial Renewal, Repair and CancerR01CA169086 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI THAYER, SARAH P · 2013 to 2017
$1.6M
AUTOIMMUNE MECHANISM IN ULCERATIVE COLITISR01DK047673 · NIDDK · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI DAS, KIRON M · 1993 to 2001
$796k
NCI NIH HHS P30 CA072720NCI NIH HHS P50 CA127003NCI NIH HHS R01 CA169086NIDDK NIH HHS R01 DK063618NIDDK NIH HHS R01 DK47673NIDDK NIH HHS R01 DK63618
6 · The paper itself

Abstract

objectiveIntraductal papillary mucinous neoplasm (IPMN) consists of four epithelial subtypes that correlate with histological grades and risks for malignant transformation. mAb Das-1 is a monoclonal antibody against a colonic epithelial phenotype that is reactive to premalignant conditions of the upper GI tract. We sought to assess the ability of mAb Das-1 to identify IPMN with high risk of malignant transformation.

designmAb Das-1 reactivity was evaluated in 94 patients with IPMNs by immunohistochemistry. Lesional fluid from 38 separate patients with IPMN (n=27), low-grade non-mucinous cystic neoplasms (n=7) and pseudocysts (n=4) was analysed by ELISA and western blot.

resultsImmunohistochemistry-Normal pancreatic ducts were non-reactive and low-grade gastric-type IPMN (IPMN-G) (1/17) and intermediate-grade IPMN-G (1/23) were minimally reactive with mAb Das-1. In contrast, mAb Das-1 reactivity was significantly higher in high-risk/malignant lesions (p<0.0001) including: intestinal-type IPMN with intermediate-grade dysplasia (9/10); high-grade dysplasia of gastric (4/7), intestinal (12/12), oncocytic (2/2) and pancreatobiliary types (2/2); and invasive tubular (8/12), colloid (7/7) and oncocytic (2/2) carcinoma. The sensitivity and specificity of mAb Das-1 for high-risk/malignant IPMNs were 85% and 95%, respectively. Lesional fluid-Samples from low- and intermediate-grade IPMN-G (n=9), and other low-grade/benign non-mucinous lesions demonstrated little reactivity with mAb Das-1. Conversely, cyst fluid from high-risk/malignant IPMNs (n=18) expressed significantly higher reactivity (p<0.0001). The sensitivity and specificity of mAbDas-1 in detecting high-risk/malignant IPMNs were 89% and 100%, respectively.

conclusionsmAb Das-1 reacts with high specificity to tissue and cyst fluid from high-risk/malignant IPMNs and thus may help in preoperative clinical risk stratification.

Indexed as

Antibody SpecificityAdenocarcinoma, MucinousAdultAgedAntibodiesBiomarkers, TumorBlotting, WesternCarcinoma, Pancreatic DuctalCarcinoma, PapillaryEnzyme-Linked Immunosorbent AssayFemaleHumansImmunohistochemistryMaleMiddle AgedPancreatic NeoplasmsAntibodiesBiomarkers, TumorDAS-1 protein, humanPancreatic CancerPancreatic PathologyPancreatic Tumours

Identifiers

PMID24277729
PMCPMC5614500
OpenAlexW2137714512

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Read underepoch 390

Registered trials

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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.