Evidence map›Paper›PMID 27800600›Full record

ArticleBiotechnology and bioengineering2017

Cholestyramine as a promising, strong anion exchange resin for direct capture of genetic biomarkers from raw pancreatic fluids.

Andrew J Hilmer, R Brooke Jeffrey, Walter G Park, Chaitan Khosla

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 83% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Bile acids and microbes in metabolic disease.World journal of gastroenterology · 2022
    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

4 authors at 2 institutions in 1 country.

Andrew J HilmerDepartments of Chemistry, Chemical Engineering, and Biochemistry, Stanford University, Stanford 94305, California.
R Brooke JeffreyDepartment of Radiology, Stanford University Medical Center, Stanford, California.
Walter G ParkDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Stanford, California.
Chaitan KhoslaDepartments of Chemistry, Chemical Engineering, and Biochemistry, Stanford University, Stanford 94305, California.
Stanford Medicine · USStanford University · US

Funding

Role of Transglutaminase 2 in Celiac SprueR01DK063158 · NIDDK · STANFORD UNIVERSITY · PI CHAITAN KHOSLA · 2003 to 2026
$11.2M
Microfluidic Immunoassay for Enabling In Vivo Gastrointestinal DiagnosticsF32DK101211 · NIDDK · STANFORD UNIVERSITY · PI HILMER, ANDREW J. · 2014 to 2015
$94k
NIDDK NIH HHS F32 DK101211NIDDK NIH HHS R01 DK063158
6 · The paper itself

Abstract

The ability to capture cell-free DNA from the gastrointestinal tract, in a minimally invasive manner, could enhance our ability to diagnose gastrointestinal disease, or gain a better understanding of the spatial mapping of the intestinal microbiota. We, therefore, sought to identify a class of capture agents that could directly and efficiently sequester genetic material from intestinal fluids. As a particular case study, we examined the ability to capture DNA from pancreatic secretions, for potential application in enabling the sequestration of early, genetic biomarkers of pancreatic disease. We hypothesized that the cholestyramine series of strong cation exchange resins, which are FDA approved for the treatment of high cholesterol, may be capable of capturing DNA from pancreatic secretions. We identified a particular cholestyramine resin, DOWEX 1 × 2 100-200 mesh, which is able to efficiently capture and purify DNA from pancreatic fluid. Using only 200 μL of pancreatic secretions, we are able to recover 247 ± 182 ng of amplifiable human DNA, giving an estimated pancreatic fluid DNA content of 1.23 ± 0.91 ng/μL. To our knowledge, this is the first demonstration of a material that can effectively capture and purify DNA directly from untreated pancreatic fluids. Thus, our approach could hold high utility for the in vivo capture of DNA and disease biomarkers if incorporated into an appropriate sampling device. Biotechnol. Bioeng. 2017;114: 934-938. © 2016 Wiley Periodicals, Inc.

Indexed as

Anion Exchange ResinsCell LineCholestyramine ResinDNAGenetic MarkersHumansModels, BiologicalPancreatic JuiceAnion Exchange ResinsCholestyramine ResinDNAGenetic Markersbiomarkercell-free DNA capturecholestyramineintestinepancreatic fluid

Identifiers

PMID27800600
PMCPMC5503842
OpenAlexW2555475360

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.