Evidence map›Paper›PMID 36232908›Full record

ArticleInternational journal of molecular sciences2022

Methodological and Biological Factors Influencing Global DNA Methylation Results Measured by LINE-1 Pyrosequencing Assay in Colorectal Tissue and Liquid Biopsy Samples.

Krisztina A Szigeti, Barbara K Barták, Zsófia B Nagy, Sára Zsigrai, Márton Papp, Eszter Márkus, Peter Igaz, István Takács, Béla Molnár, Alexandra Kalmár

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Krisztina A SzigetiDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Barbara K BartákDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Zsófia B NagyDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Sára ZsigraiDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Márton PappCentre for Bioinformatics, University of Veterinary Medicine Budapest, 1078 Budapest, Hungary.ORCID 0000-0003-4975-253X
Eszter MárkusDepartment of Anaesthesia and Intensive Care, Pest County Flor Ferenc Hospital, 2143 Kistarcsa, Hungary.
Peter IgazDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0003-2192-554X
István TakácsDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Béla MolnárDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Alexandra KalmárDepartment of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Semmelweis University · HUJahn Ferenc Dél-Pesti Kórház és Rendelőintézet · HUUniversity of Veterinary Medicine · HU

Funding

ational Research, Development, and Innovation Fund by the Ministry of Innovation and Technology of Hungary TKP2021-EGA-24HUNGARIAN NATIONAL OFFICE FOR RESEARCH AND TECHNOLOGY (NKVP_16-1-2016-0004 GRANT)
6 · The paper itself

Abstract

Long interspersed nuclear element 1 (LINE-1) bisulfite pyrosequencing is a widely used technique for genome-wide methylation analyses. We aimed to investigate the effects of experimental and biological factors on its results to improve the comparability. LINE-1 bisulfite pyrosequencing was performed on colorectal tissue (n = 222), buffy coat (n = 39), and plasma samples (n = 9) of healthy individuals and patients with colorectal tumors. Significantly altered methylation was observed between investigated LINE-1 CpG positions of non-tumorous tissues (p ≤ 0.01). Formalin-fixed, paraffin-embedded biopsies (73.0 ± 5.3%) resulted in lower methylation than fresh frozen samples (76.1 ± 2.8%) (p ≤ 0.01). DNA specimens after long-term storage showed higher methylation levels (+3.2%, p ≤ 0.01). In blood collection tubes with preservatives, cfDNA and buffy coat methylation significantly changed compared to K3EDTA tubes (p ≤ 0.05). Lower methylation was detected in older (>40 years, 76.8 ± 1.7%) vs. younger (78.1 ± 1.0%) female patients (p ≤ 0.05), and also in adenomatous tissues with MTHFR 677CT, or 1298AC mutations vs. wild-type (p ≤ 0.05) comparisons. Based on our findings, it is highly recommended to consider the application of standard DNA samples in the case of a possible clinical screening approach, as well as in experimental research studies.

Indexed as

Cell-Free Nucleic AcidsColorectal NeoplasmsAgedBiological FactorsBiopsyDNADNA MethylationFemaleFormaldehydeHigh-Throughput Nucleotide SequencingHumansLiquid BiopsyLong Interspersed Nucleotide ElementsMaleSulfitesBiological FactorsCell-Free Nucleic AcidsDNAFormaldehydehydrogen sulfiteSulfitescolorectal cancerglobal DNA methylationLINE-1 bisulfite pyrosequencinglong interspersed nuclear element-1

Identifiers

PMID36232908
PMCPMC9569782
OpenAlexW4303699500

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.