Evidence map›Paper›PMID 31867127›Full record

ArticleEpigenomes2017

Helicase Lymphoid-Specific Enzyme Contributes to the Maintenance of Methylation of SST1 Pericentromeric Repeats That Are Frequently Demethylated in Colon Cancer and Associate with Genomic Damage.

Johanna K Samuelsson, Gabrijela Dumbovic, Cristian Polo, Cristina Moreta, Andreu Alibés, Tatiana Ruiz-Larroya, Pepita Giménez-Bonafé, Sergio Alonso, Sonia-V Forcales, Perucho Manuel

Abstract read
In one paragraph

Article in Epigenomes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The Current State of Chromatin Immunoprecipitation (ChIP) from FFPE Tissues.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Review
  8. Article
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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

10 authors.

Johanna K SamuelssonSanford-Burnham-Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
Gabrijela DumbovicInstitute of Predictive and Personalized Medicine of Cancer (IMPPC), Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Badalona 08916, Barcelona, Spain.
Cristian PoloInstitute of Predictive and Personalized Medicine of Cancer (IMPPC), Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Badalona 08916, Barcelona, Spain.
Cristina MoretaInstitute of Predictive and Personalized Medicine of Cancer (IMPPC), Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Badalona 08916, Barcelona, Spain.
Andreu AlibésInstitute of Predictive and Personalized Medicine of Cancer (IMPPC), Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Badalona 08916, Barcelona, Spain.
Tatiana Ruiz-LarroyaSanford-Burnham-Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
Pepita Giménez-BonaféDepartament de Ciències Fisiòlogiques, Facultat de Medicina i Ciències de la Salut, Campus Ciències de la Salut, Bellvitge, Universitat de Barcelona, Hospitalet del Llobregat 08916, Barcelona, Spain.
Sergio AlonsoInstitute of Predictive and Personalized Medicine of Cancer (IMPPC), Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Badalona 08916, Barcelona, Spain.
Sonia-V ForcalesInstitute of Predictive and Personalized Medicine of Cancer (IMPPC), Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Badalona 08916, Barcelona, Spain.
Perucho ManuelSanford-Burnham-Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.

Funding

MOLECULAR PATHOGENESIS OF CANCER OF MUTATOR PHENOTYPER37CA063585 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PERUCHO, MANUEL · 1999 to 2008
$7.0M
NCI NIH HHS R37 CA063585
6 · The paper itself

Abstract

DNA hypomethylation at repetitive elements accounts for the genome-wide DNA hypomethylation common in cancer, including colorectal cancer (CRC). We identified a pericentromeric repeat element called SST1 frequently hypomethylated (>5% demethylation compared with matched normal tissue) in several cancers, including 28 of 128 (22%) CRCs. SST1 somatic demethylation associated with genome damage, especially in tumors with wild-type

Indexed as

colorectal cancerDNA demethylationepigeneticssatellite element

Identifiers

PMID31867127
PMCPMC6924650

What OpenQuestion holds

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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.