Evidence map›Paper›PMID 33905828›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2021

Solid-state nanopore analysis of human genomic DNA shows unaltered global 5-hydroxymethylcytosine content associated with early-stage breast cancer.

Osama K Zahid, Felipe Rivas, Fanny Wang, Komal Sethi, Katherine Reiss, Samuel Bearden, Adam R Hall

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 38% 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, 10 citations in OpenAlex.

  1. Review
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  4. Article
  5. Mechanisms that regulate the activities of TET proteins.Cellular and molecular life sciences : CMLS · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Osama K ZahidVirginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Felipe RivasVirginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Fanny WangVirginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Komal SethiVirginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Katherine ReissDepartment of Engineering, Wake Forest University, Winston-Salem, NC, USA.
Samuel BeardenVirginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Adam R HallVirginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA; Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, USA. Electronic address: arhall@wakehealth.edu.
Virginia Tech - Wake Forest University School of Biomedical Engineering & Sciences · USWake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Detecting diverse nucleic acid biomarkers of cancer with solid-state nanoporesR33CA246448 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HALL, ADAM ROGER · 2020 to 2020
$1.1M
Redox Biology and Medicine Training ProgramT32GM127261 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, POOLE, LESLIE B · 2018 to 2022
$975k
Molecular Detection of DNA Hydroxymethylation for Cancer ScreeningR21CA193067 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HALL, ADAM ROGER · 2015 to 2017
$649k
NCI NIH HHS P30 CA012197NCI NIH HHS R21 CA193067NCI NIH HHS R33 CA246448NIGMS NIH HHS T32 GM127261
6 · The paper itself

Abstract

5-Hydroxymethylcytosine (5hmC), the first oxidized form of the well-known epigenetic modification 5-methylcytosine, is an independent regulator of gene expression and therefore a potential marker for disease. Here, we report on methods developed for a selective solid-state nanopore assay that enable direct analysis of global 5hmC content in human tissue. We first describe protocols for preparing genomic DNA derived from both healthy breast tissue and stage 1 breast tumor tissue and then use our approach to probe the net abundance of the modified base in each cohort. Then, we employ empirical data to adjust for the impact of nanopore diameter on the quantification. Correcting for variations in nanopore diameter among the devices used for analysis reveals no detectable difference in global 5hmC content between healthy and tumor tissue. These results suggest that 5hmC changes may not be associated with early-stage breast cancer and instead are a downstream consequence of the disease.

Indexed as

Genome, HumanNanopore Sequencing5-MethylcytosineBreast NeoplasmsDNA, NeoplasmFemaleHumansMCF-7 CellsNeoplasm Staging5-hydroxymethylcytosine5-MethylcytosineDNA, NeoplasmCancerEpigeneticsHydroxymethylcytosineSolid-state nanopore

Identifiers

PMID33905828
PMCPMC8238847
OpenAlexW3158635564

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.