Evidence map›Paper›PMID 24161315›Full record

ArticleJournal of immunological methods2013

Multiplexed VeraCode bead-based serological immunoassay for colorectal cancer.

Heather P Ostendorff, Amany Awad, Karen I Braunschweiger, Ziying Liu, Zhi Wan, Kenneth J Rothschild, Mark J Lim

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunological methods, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. ELISA in the multiplex era: potentials and pitfalls.Proteomics. Clinical applications · 2015
    Review
  5. Article
  6. 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

7 authors at 2 institutions in 1 country.

Heather P OstendorffAmberGen, Inc., 313 Pleasant Street, Watertown, MA 02472, USA.
Amany Awad
Karen I Braunschweiger
Ziying Liu
Zhi Wan
Kenneth J Rothschild
Mark J Lim
Ambergen (United States) · USBoston University · US

Funding

Proteome Bead-Display for Discovery of Tumor AntigensR44CA137948 · NCI · AMBERGEN, INC · PI LIM, MARK · 2012 to 2014
$1.5M
Proteome Bead-Display for Discovery of Tumor AntigensR43CA137948 · NCI · AMBERGEN, INC · PI LIM, MARK · 2010 to 2010
$188k
NCI NIH HHS R43 CA137948NCI NIH HHS R43/R44 CA137948NCI NIH HHS R44 CA137948
6 · The paper itself

Abstract

Colorectal cancer (CRC) is the second leading cause of cancer deaths in the US and Western world. Despite increased screening and advances in treatment, the mortality rate (ca. 50,000/year) and high national health-care burden for CRC are likely to remain high unless an effective non-invasive screening test for CRC is instituted for a large segment of the population. Blood-based protein biomarkers hold great promise for early disease diagnosis and personalized medicine; yet robust and reproducible multiplexing platforms and methodologies have lagged behind their genomic counterparts. Here, we report the development of a novel, multiplexed, hybrid immunoassay for CRC that is formatted on barcoded VeraCode™ micro-beads, which have until now only been used for genomic assays. The method combines a sandwich immunoassay format for detection of serum protein biomarkers with an antigen assay for autoantibody detection. The serum protein biomarkers CEA and GDF15 as well as autoantibodies to the p53 tumor associated antigen (TAA) were used to exemplify the method. This multiplex biomarker panel was configured to run on Illumina's holographically barcoded VeraCode™ micro-bead platform, which is capable of measuring hundreds of analytes simultaneously in a single well from small volumes of blood (<50 μL) using a 96-well industry standard microtiter plate. This novel use of the VeraCode™ micro-bead platform translates into a potentially low volume, high throughput, multiplexed assay for CRC, for the purposes of biomarker validation, as well as patient screening, diagnostics and prognostics. In an evaluation of a 186 patient sera training set (CRC and normal), we obtained a diagnostic sensitivity of 54% and a specificity of 98%. We anticipate that by expanding and refining the biomarkers in this initial panel, and performing more extensive clinical validations, such an assay could ultimately provide a basis for CRC population screening to complement the more invasive, expensive and low throughput (but highly sensitive and specific) colonoscopy.

Indexed as

AutoantibodiesBiomarkers, TumorCarcinoembryonic AntigenColorectal NeoplasmsEarly Detection of CancerEnzyme-Linked Immunosorbent AssayGrowth Differentiation Factor 15High-Throughput Screening AssaysHumansImmunologic TestsMicrospheresMiniaturizationReproducibility of ResultsSensitivity and SpecificityTumor Suppressor Protein p53AutoantibodiesBiomarkers, TumorCarcinoembryonic AntigenGDF15 protein, humanGrowth Differentiation Factor 15Tumor Suppressor Protein p53AutoantibodiesBiomarkercarcinoembryonic antigenCEAcolorectal cancerColorectal cancerCRCGDF15growth differentiation factor 15Multiplex immunoassayTAAstumor associated antigensTumor-associated antigens

Identifiers

PMID24161315
PMCPMC3867820
OpenAlexW2035176621

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.