Evidence map›Paper›PMID 28407691›Full record

ArticleOncotarget2017

TET2 and MEG3 promoter methylation is associated with acute myeloid leukemia in a Hainan population.

Hongxia Yao, Mengling Duan, Lie Lin, Congming Wu, Xiangjun Fu, Hua Wang, Li Guo, Wenting Chen, Li Huang, Dan Liu and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  5. Lower Levels of TET2 Gene Expression, with a Higher Level of TET2 Promoter Methylation in Patients with AML; Evidence for the Role of Aberrant Methylation in AML Pathogenesis.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2024
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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

13 authors at 1 institution in 1 country.

Hongxia YaoDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Mengling DuanDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Lie LinDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Congming WuDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Xiangjun FuDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Hua WangDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Li GuoDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Wenting ChenDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Li HuangDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Dan LiuDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Ruo RaoDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Shuwen WangDepartment of Hematology, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Yipeng DingDepartment of Emergency, Hainan General Hospital, Haikou, Hainan, 570311, R.R. China.
Hainan General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The promoter of MEG3, which encodes the long non-coding RNA (lncRNA) MEG3, is often hypermethylated in acute myeloid leukemia (AML). Additionally, the Tet methylcytosine dioxygenase 2 gene (TET2) is frequently inactivated, which can lead to impaired DNA methylation and promote AML development. We examined the association between TET2 and MEG3 promoter hypermethylation in Hainan patients with AML. The expression of MEG3, TET2, miR-22-3p, and miR-22-5p was assessed in bone marrow samples from AML patients and healthy controls using real-time quantitative PCR. Using Sequenom MassARRAY technology, we compared MEG3 promoter methylation in AML patients and healthy controls. MEG3 expression was lower in AML patients than in the controls (P = 0.136). Moreover, there was greater methylation of MEG3 promoter in the AML patients than the controls (P < 0.05). Methylation of the MEG3 promoter correlated negatively with TET2 expression (P < 0.05, r < 0). Likewise there was a negative correlation between TET2 activity and MEG3 promoter methylation (P < 0.05, r < 0). These results suggest that hypermethylation of the MEG3 promoter in AML may result from decreased TET2 activity. These data provide insight into the molecular mechanisms underlying AML development and progression.

Indexed as

DNA MethylationCase-Control StudiesCell Line, TumorChinaDioxygenasesDNA-Binding ProteinsHumansLeukemia, Myeloid, AcuteMicroRNAsPromoter Regions, GeneticProto-Oncogene ProteinsRNA, Long NoncodingDioxygenasesDNA-Binding ProteinsMEG3 non-coding RNA, humanMicroRNAsMIRN22 microRNA, humanProto-Oncogene ProteinsRNA, Long NoncodingTET2 protein, humanAMLHainanLncRNA MEG3rtPCRTET2

Identifiers

PMID28407691
PMCPMC5392332
OpenAlexW2590962532

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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.