Evidence map›Paper›PMID 27528035›Full record

ArticleOncotarget2016

Evaluation of DNMT3A genetic polymorphisms as outcome predictors in AML patients.

Xiao-Qing Yuan, Dao-Yu Zhang, Han Yan, Yong-Long Yang, Ke-Wei Zhu, Yan-Hong Chen, Xi Li, Ji-Ye Yin, Xiao-Lin Li, Hui Zeng and 1 more

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 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
2.7field-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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

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  5. Medicina (Kaunas, Lithuania) · 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

11 authors at 3 institutions in 1 country.

Xiao-Qing YuanDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Dao-Yu ZhangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Han YanDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Yong-Long YangDepartment of Pharmacy, Haikou People's Hospital and Affiliated Haikou Hospital of Xiangya Medical School, Central South University, Haikou 570311, P. R. China.
Ke-Wei ZhuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Yan-Hong ChenDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Xi LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Ji-Ye YinDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Xiao-Lin LiDepartment of Hematology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Hui ZengDepartment of Hematology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Xiao-Ping ChenDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Central South University · CNXiangya Hospital Central South University · CNHaikou City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNMT3A mutation is known as a recurrent event in acute myelogenous leukemia (AML) patients. However, association between DNMT3A genetic polymorphisms and AML patients' outcomes is unknown. DNMT3A 11 SNPs (rs11695471, rs2289195, rs734693, rs2276598, rs1465825, rs7590760, rs13401241, rs7581217, rs749131, rs41284843 and rs7560488) were genotyped in 344 diagnostic non-FAB-M3 AML patients from southern China. Patients underwent combined chemotherapy with cytarabine and anthracyclines. DNMT3A mRNA expression was analyzed in PBMCs from randomly selected AML patients. Multivariate analysis and combined genotype analysis showed that rs2276598 was associated with increased while rs11695471 and rs734693 were associated with decreased chemosensitivity (P<0.05), while rs11695471 (worse for OS), rs2289195 (favorable for OS and DFS) and rs2276598 (favorable for DFS) were significantly associated with disease prognosis (P<0.05). In conclusion, DNMT3A polymorphisms may be potential predictive markers for AML patients' outcomes, which might improve prognostic stratification of AML.

Indexed as

GenotypeAdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsChinaDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansLeukemia, Myeloid, AcuteMaleMiddle AgedPolymorphism, Single NucleotideDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNMT3A protein, humanAMLchemosensitivityDNMT3Apolymorphismprognosis

Identifiers

PMID27528035
PMCPMC5312402
OpenAlexW2517114205

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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.