Evidence map›Paper›PMID 27738314›Full record

ArticleOncotarget2016

Loss of UHRF2 expression is associated with human neoplasia, promoter hypermethylation, decreased 5-hydroxymethylcytosine, and high proliferative activity.

Huarui Lu, Sweta Bhoopatiraju, Hongbo Wang, Nolan P Schmitz, Xiaohong Wang, Matthew J Freeman, Colleen L Forster, Michael R Verneris, Michael A Linden, Timothy C Hallstrom

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. UHRF2 accumulates in early GCell cycle (Georgetown, Tex.) · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. The UHRF protein family in epigenetics, development, and carcinogenesis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Dietary Modulation of the Epigenome.Physiological reviews · 2018
    Review
  16. Article
  17. Article
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 1 institution in 1 country.

Huarui LuDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Sweta BhoopatirajuDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Hongbo WangDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Nolan P SchmitzDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Xiaohong WangDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Matthew J FreemanDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Colleen L ForsterBioNet, Academic Health Center, University of Minnesota, Minneapolis, MN 55455, USA.
Michael R VernerisDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Michael A LindenDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA.
Timothy C HallstromDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
University of Minnesota · US

Funding

Cell Fate Control by Integrated E2F, FoxO and PI3K Signaling in RetinoblastomaR01CA168622 · NCI · UNIVERSITY OF MINNESOTA · PI HALLSTROM, TIMOTHY C. · 2013 to 2017
$1.6M
NCI NIH HHS R01 CA168622
6 · The paper itself

Abstract

Ubiquitin-like with PHD and ring finger domains 2 (UHRF2) binds to 5-hydroxymethylcytosine (5hmC), a DNA base involved in tissue development, but it is unknown how their distribution compares with each other in normal and malignant human tissues. We used IHC on human tumor specimens (160 from 19 tumor types) or normal tissue to determine the expression and distribution of UHRF2, Ki-67, and 5hmC. We also examined UHRF2 expression in cord blood progenitors and compared its expression to methylation status in 6 leukemia cell lines and 15 primary human leukemias. UHRF2 is highly expressed, paralleling that of 5hmC, in most non-neoplastic, differentiated tissue with low Ki-67 defined proliferative activity. UHRF2 is expressed in common lymphoid progenitors and mature lymphocytes but not common myeloid progenitors or monocytes. In contrast, UHRF2 immunostaining in human cancer tissues revealed widespread reduction or abnormal cytoplasmic localization which correlated with a higher Ki-67 and reduced 5hmC. UHRF2 expression is reduced in some leukemia cell lines, this correlates with promoter hypermethylation, and similar UHRF2 methylation profiles are seen in primary human leukemia samples. Thus, UHRF2 and 5hmC are widely present in differentiated human tissues, and UHRF2 protein is poorly expressed or mislocalized in diverse human cancers.

Indexed as

DNA MethylationPromoter Regions, Genetic5-MethylcytosineBiomarkers, TumorCell Line, TumorCell ProliferationEpigenesis, GeneticGene Expression Regulation, NeoplasticHumansLymphocytesLymphoid Progenitor CellsNeoplasm GradingNeoplasmsProtein TransportUbiquitin-Protein Ligases5-hydroxymethylcytosine5-MethylcytosineBiomarkers, TumorUbiquitin-Protein LigasesUHRF2 protein, human5-hydroxymethylcytosineleukemiaubiquitin-like with PHD and ring finger domains 2UHRF1UHRF2

Identifiers

PMID27738314
PMCPMC5340178
OpenAlexW2530270121

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.