Evidence map›Paper›PMID 25210800›Full record

ArticleCell death & disease2014

MEIS2 is essential for neuroblastoma cell survival and proliferation by transcriptional control of M-phase progression.

Y Zha, Y Xia, J Ding, J-H Choi, L Yang, Z Dong, C Yan, S Huang, H-F Ding

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

38 citing papers in PubMed, 58 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Y ZhaDepartment of Neurology, The First Hospital of Yichang, Institute of Translational Neuroscience, Three Gorges University College of Medicine, Yichang, China.
Y Xia1] Department of Neurology, The First Hospital of Yichang, Institute of Translational Neuroscience, Three Gorges University College of Medicine, Yichang, China [2] Cancer Center, Georgia Regents University, Augusta, GA, USA.
J DingCancer Center, Georgia Regents University, Augusta, GA, USA.
J-H Choi1] Cancer Center, Georgia Regents University, Augusta, GA, USA [2] Department of Biostatistics and Epidemiology, Georgia Regents University, Augusta, GA, USA.
L YangState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and System Biology, Southwest University, Chongqing, China.
Z DongDepartment of Cellular Biology and Anatomy, Georgia Regents University, Augusta, GA, USA.
C Yan1] Cancer Center, Georgia Regents University, Augusta, GA, USA [2] Department of Biochemistry and Molecular Biology, Georgia Regents University, Augusta, GA, USA.
S HuangDepartment of Biochemistry and Molecular Biology, Georgia Regents University, Augusta, GA, USA.
H-F Ding1] Cancer Center, Georgia Regents University, Augusta, GA, USA [2] Department of Pathology, Medical College of Georgia, Georgia Regents University, Augusta, GA, USA.
Georgia Regents Medical Center · USAugusta University · USState Key Laboratory of Silkworm Genomic Biology

Funding

The oncogenic basis of Bmi-1 in neuroblastoma developmentR01CA124982 · NCI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI DING, HAN-FEI · 2007 to 2010
$1.1M
NCI NIH HHS R01 CA124982NCI NIH HHS R01CA124982
6 · The paper itself

Abstract

MEIS2 has an important role in development and organogenesis, and is implicated in the pathogenesis of human cancer. The molecular basis of MEIS2 action in tumorigenesis is not clear. Here, we show that MEIS2 is highly expressed in human neuroblastoma cell lines and is required for neuroblastoma cell survival and proliferation. Depletion of MEIS2 in neuroblastoma cells leads to M-phase arrest and mitotic catastrophe, whereas ectopic expression of MEIS2 markedly enhances neuroblastoma cell proliferation, anchorage-independent growth, and tumorigenicity. Gene expression profiling reveals an essential role of MEIS2 in maintaining the expression of a large number of late cell-cycle genes, including those required for DNA replication, G2-M checkpoint control and M-phase progression. Importantly, we identify MEIS2 as a transcription activator of the MuvB-BMYB-FOXM1 complex that functions as a master regulator of cell-cycle gene expression. Further, we show that FOXM1 is a direct target gene of MEIS2 and is required for MEIS2 to upregulate mitotic genes. These findings link a developmentally important gene to the control of cell proliferation and suggest that high MEIS2 expression is a molecular mechanism for high expression of mitotic genes that is frequently observed in cancers of poor prognosis.

Indexed as

Cell DivisionCell ProliferationCell SurvivalUp-RegulationCell Cycle ProteinsCell Line, TumorForkhead Box Protein M1Forkhead Transcription FactorsHomeodomain ProteinsHumansNeuroblastomaTranscription FactorsCell Cycle ProteinsForkhead Box Protein M1Forkhead Transcription FactorsFOXM1 protein, humanHomeodomain ProteinsMEIS2 protein, humanTranscription Factors

Identifiers

PMID25210800
PMCPMC4540202
OpenAlexW2002536280

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.