Evidence map›Paper›PMID 25441900›Full record

ArticleAnalytica chimica acta2014

Quantification of 5-methylcytosine, 5-hydroxymethylcytosine and 5-carboxylcytosine from the blood of cancer patients by an enzyme-based immunoassay.

Basudev Chowdhury, Il-Hoon Cho, Noah Hahn, Joseph Irudayaraj

Abstract readValidation Study
In one paragraph

Article in Analytica chimica acta, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

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  13. Clinical Significance of TET2 in Female Cancers.Frontiers in bioengineering and biotechnology · 2022
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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.

Basudev ChowdhuryBindley Bioscience & Birck Nanotechnology Center, Department of Agricultural & Biological Engineering, Purdue University, 225 South University Street, West Lafayette, IN 47907, USA.
Il-Hoon ChoBindley Bioscience & Birck Nanotechnology Center, Department of Agricultural & Biological Engineering, Purdue University, 225 South University Street, West Lafayette, IN 47907, USA; Dept. of Biomedical Laboratory Science, College of Health Science, Eulji University, Seongnam 461-713, Republic of Korea.
Noah HahnIndiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN 46202, USA.
Joseph IrudayarajBindley Bioscience & Birck Nanotechnology Center, Department of Agricultural & Biological Engineering, Purdue University, 225 South University Street, West Lafayette, IN 47907, USA. Electronic address: josephi@purdue.edu.

Funding

Indiana Clinical and Translational Science Institute (UL1)UL1TR000006 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI SHEKHAR, ANANTHA · 2012 to 2013
$5.6M
Interdisciplinary Cancer Prevention Research Internship ProgramR25CA128770 · NCI · PURDUE UNIVERSITY · PI TEEGARDEN, DOROTHY · 2008 to 2012
$1.5M
Label-free, real-time detection of kinase activity in vitro and in single cells uR21CA157395 · NCI · PURDUE UNIVERSITY · PI IRUDAYARAJ, JOSEPH MK · 2011 to 2013
$610k
NCATS NIH HHS TR000006NCATS NIH HHS UL1 TR000006NCI NIH HHS R21 CA157395NCI NIH HHS R25 CA128770NCI NIH HHS R25CA128770
6 · The paper itself

Abstract

backgroundGenome-wide aberrations of the classic epigenetic modification 5-methylcytosine (5mC), considered the hallmark of gene silencing, has been implicated to play a pivotal role in mediating carcinogenic transformation of healthy cells. Recently, three epigenetic marks derived from enzymatic oxidization of 5mC namely 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC) and 5-carboxylcytosine (5caC), have been discovered in the mammalian genome. Growing evidence suggests that these novel bases possess unique regulatory functions and may play critical roles in carcinogenesis.

methodsTo provide a quantitative basis for these rare epigenetic marks, we have designed a biotin-avidin mediated enzyme-based immunoassay (EIA) and evaluated its performance in genomic DNA isolated from blood of patients diagnosed with metastatic forms of lung, pancreatic and bladder cancer, as well as healthy controls. The proposed EIA incorporates spatially optimized biotinylated antibody and a high degree of horseradish-peroxidase (HRP) labeled streptavidin, facilitating signal amplification and sensitive detection.

resultsWe report that the percentages of 5mC, 5hmC and 5caC present in the genomic DNA of blood in healthy controls as 1.025±0.081, 0.023±0.006 and 0.001±0.0002, respectively. We observed a significant (p<0.05) decrease in the mean global percentage of 5hmC in blood of patients with malignant lung cancer (0.013±0.003%) in comparison to healthy controls.

conclusionThe precise biological roles of these epigenetic modifications in cancers are still unknown but in the past two years it has become evident that the global 5hmC content is drastically reduced in a variety of cancers. To the best of our knowledge, this is the first report of decreased 5hmC content in the blood of metastatic lung cancer patients and the clinical utility of this observation needs to be further validated in larger sample datasets.

Indexed as

5-MethylcytosineCytosineDNAEpigenesis, GeneticHumansImmunoenzyme TechniquesLimit of DetectionNeoplasms5-carboxylcytosine5-hydroxymethylcytosine5-MethylcytosineCytosineDNA5-Carboxylcytosine (5caC)5-Formylcytosine (5fC)5-Hydroxymethylcytosine (5hmC)5-Methylcytosine (5mC)CancerEnzyme-based Immunoassay (EIA)Epigenetic modifications

Identifiers

PMID25441900
PMCPMC4254572

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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.