Evidence map›Paper›PMID 29735550›Full record

ArticleCancer research2018

miR-339 Promotes Development of Stem Cell Leukemia/Lymphoma Syndrome via Downregulation of the

Tianxiang Hu, Yating Chong, Sumin Lu, Rebecca Wang, Haiyan Qin, Jeane Silva, Eiko Kitamura, Chang-Sheng Chang, LesleyAnn Hawthorn, John K Cowell

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

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  9. CPT1B, a metabolic molecule, is also an independent risk factor in CN-AML.Cancer biomarkers : section A of Disease markers · 2023
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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 at 1 institution in 1 country.

Tianxiang HuGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Yating ChongGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Sumin LuGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Rebecca WangGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Haiyan QinGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Jeane SilvaGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Eiko KitamuraGeorgia Cancer Center, Augusta University, Augusta, Georgia.
Chang-Sheng ChangGeorgia Cancer Center, Augusta University, Augusta, Georgia.
LesleyAnn HawthornGeorgia Cancer Center, Augusta University, Augusta, Georgia.
John K CowellGeorgia Cancer Center, Augusta University, Augusta, Georgia. jcowell@augusta.edu.
Augusta University Health · US

Funding

GENETIC ANALYSIS OF MYELOPROLIFERATIVE DISEASER01CA076167 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI COWELL, JOHN K · 1999 to 2024
$6.2M
NCI NIH HHS R01 CA076167
6 · The paper itself

Abstract

The development of myeloid and lymphoid neoplasms related to overexpression of FGFR1 kinases as a result of chromosome translocations depends on the promotion of a stem cell phenotype, suppression of terminal differentiation, and resistance to apoptosis. These phenotypes are related to the stem cell leukemia/lymphoma syndrome (SCLL), which arises through the effects of the activated FGFR1 kinase on gene transcription, which includes miRNA dysregulation. In a screen for miRNAs that are directly regulated by FGFR1, and which stimulate cell proliferation and survival, we identified miR-339-5p, which is highly upregulated in cells carrying various different chimeric kinases. Overexpression of miR-339-5p in SCLL cell types enhances cell survival and inhibition of its function leads to reduced cell viability. miR-339-5p overexpression protects cells from the consequences of FGFR1 inactivation, promoting cell-cycle progression and reduced apoptosis. Transient luciferase reporter assays and qRT-PCR detection of endogenous miR-339-5p expression in stably transduced cell lines demonstrated that BCR-FGFR1 can directly regulate miR-339-5p expression. This correlation between miR-339-5p and FGFR1 expression is also seen in primary human B-cell precursor acute lymphoblastic leukemia. In a screen to identify targets of miR-339-5p, we identified and verified the

Indexed as

Animalsbcl-2-Associated X ProteinBcl-2-Like Protein 11Cell Line, TumorCell SurvivalChromosomes, Human, Pair 8Disease Models, AnimalDown-RegulationFemaleHEK293 CellsHematopoietic Stem CellsHumansLeukemiaLymphomaMiceMice, Inbred BALB CBAX protein, humanbcl-2-Associated X ProteinBCL2L11 protein, humanBcl-2-Like Protein 11FGFR1 protein, humanMicroRNAsMIRN339 microRNA, humanOncogene Proteins, FusionReceptor, Fibroblast Growth Factor, Type 1

Identifiers

PMID29735550
PMCPMC6052880
OpenAlexW2800337568

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.