Evidence map›Paper›PMID 18573345›Full record

ReviewMethods (San Diego, Calif.)2008

Non-invasive, ultra-sensitive, high-throughput assays to quantify rare biomarkers in the blood.

Jaclyn A Freudenberg, Kathryn Bembas, Mark I Greene, Hongtao Zhang

Abstract readReview
In one paragraph

Review in Methods (San Diego, Calif.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Charting the Next Road Map for CSF Biomarkers in Alzheimer's Disease and Related Dementias.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  3. Analytical cellular pathology (Amsterdam) · 2016
    Article
  4. Review
  5. Quantitative biology of single neurons.Journal of the Royal Society, Interface · 2012
    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 1 institution in 1 country.

Jaclyn A FreudenbergDepartment of Pathology & Laboratory Medicine, University of Pennsylvania, 252 John Morgan Building, 3620 Hamilton Walk, Philadelphia, PA 19104-6082, USA.
Kathryn Bembas
Mark I Greene
Hongtao Zhang
University of Pennsylvania · US

Funding

Characterization of neural crest stem cells in human hair follicles.R01AR054593 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI XU, XIAOWEI · 2009 to 2013
$1.9M
Ultrasensitive FACTT assays for serum biomarkersR21CA116103 · NCI · UNIVERSITY OF PENNSYLVANIA · PI XU, XIAOWEI · 2007 to 2008
$389k
NCI NIH HHS R21 CA116103NIAMS NIH HHS R01 AR054593
6 · The paper itself

Abstract

Many diseases are easier to treat and control when detected at an early stage of disease progression. Often, disease-related antigens or biomarkers are shed from the primary site and present in the blood. Unfortunately, there are very few tests capable of detecting these rare biomarkers in the blood. A blood test would be very useful to diagnose the disease earlier, monitor effectiveness of treatments, predict recurrence, and monitor recurrence. There is certainly a need to develop assays that are ultra-sensitive, non-invasive, and high-throughput. Here we describe several highly sensitive immunological assays we have developed to detect rare serum antigens. Initially we created an assay named immuno-detection amplified by T7 RNA polymerase (IDAT). To enhance the effectiveness and streamline the procedure, this assay was amended to the facile amplification system termed fluorescent amplification catalyzed by T7 polymerase technique (FACTT). These assays have been used to analyze the tumor antigen HER2 and the prion protein PrPSc. They can also be applied to other tumor markers or antigens from a variety of diseases such as cardiovascular disease, rheumatoid arthritis, Alzheimer's disease, Parkinson's disease, and hepatitis. These tests are not limited to testing only serum, but may also be applicable to detecting biomarkers in tissue, saliva, urine, cerebrospinal fluid, etc. Clearly, the FACTT-based technology represents an important step in the detection of rare molecules in fluids or tissues for a variety of diseases.

Indexed as

AnimalsAntigensBiological AssayBiomarkersDiagnostic Techniques and ProceduresDNA-Directed RNA PolymerasesErb-b2 Receptor Tyrosine KinasesFluorescent DyesHumansImmunoenzyme TechniquesIntercalating AgentsPolymerase Chain ReactionPrPSc ProteinsRNA-Binding ProteinsViral ProteinsAntigensbacteriophage T7 RNA polymeraseBiomarkersDNA-Directed RNA PolymerasesErb-b2 Receptor Tyrosine KinasesFluorescent DyesIntercalating AgentsPrPSc ProteinsRNA-Binding ProteinsViral Proteins

Identifiers

PMID18573345
PMCPMC2605511
OpenAlexW2018302586

What OpenQuestion holds

Textmetadata
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.