Evidence map›Paper›PMID 23327923›Full record

ArticleBlood2013

MASL1 induces erythroid differentiation in human erythropoietin-dependent CD34+ cells through the Raf/MEK/ERK pathway.

Chutima Kumkhaek, Wulin Aerbajinai, Wenli Liu, Jianqiong Zhu, Naoya Uchida, Roger Kurlander, Matthew M Hsieh, John F Tisdale, Griffin P Rodgers

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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  10. Roco Proteins and the Parkinson's Disease-Associated LRRK2.International journal of molecular sciences · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Chutima KumkhaekMolecular and Clinical Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Wulin Aerbajinai
Wenli Liu
Jianqiong Zhu
Naoya Uchida
Roger Kurlander
Matthew M Hsieh
John F Tisdale
Griffin P Rodgers
National Heart Lung and Blood Institute · USNational Institutes of Health Clinical Center · US

Funding

Isolation, characterization, and transplantation of candidate stem cellsZIAHL006009 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI TISDALE, JOHN · 2009 to 2025
$13.5M
Quantitation Of Residual Tumor In Patients Undergoing Allo-transplantationZIDCL010332 · CLC · CLINICAL CENTER · PI KURLANDER, ROGER J · 2009 to 2015
$0k
Quantitating Engraftment Of Donor Hematopoietic Cells After TransplantationZIDCL010334 · CLC · CLINICAL CENTER · PI KURLANDER, ROGER J · 2009 to 2015
$0k
Intramural NIH HHS
6 · The paper itself

Abstract

Human erythropoiesis is a dynamic and complex multistep process involving differentiation of early erythroid progenitors into enucleated RBCs. The mechanisms underlying erythropoiesis still remain incompletely understood. We previously demonstrated that erythropoietin-stimulated clone-1, which is selectively expressed in normal human erythroid-lineage cells, shares 99.5% identity with malignant fibrous histiocytoma-amplified sequences with leucine-rich tandem repeats 1 (MASL1). In this study, we hypothesized that the MASL1 gene plays a role in erythroid differentiation, and used a human erythroid cell culture system to explore this concept. MASL1 mRNA and protein expression levels were significantly increased during the erythroid differentiation of CD34(+) cells following erythropoietin (EPO) treatment. Conversely, MASL1 knockdown reduced erythroid differentiation in EPO-treated CD34(+) cells. In addition, MASL1 knockdown interrupted the Raf/MEK/ERK signaling pathway in CD34(+) cells. MASL1 mutant-transfected CD34(+) cells also showed decreased erythroid differentiation. Furthermore, inhibition of the SH3 domain of Son of Sevenless, which is an upstream adapter protein in EPO-induced erythroid differentiation, also reduced MASL1 expression and phosphorylation of Raf/MEK/ERK kinases that consequently reduced erythroid differentiation of EPO-induced CD34(+) cells. Importantly, we also demonstrated that MASL1 interacts physically with Raf1. Taken together, our data provide novel insights into MASL1 regulation of erythropoiesis through the Raf/MEK/ERK pathway.

Indexed as

ErythropoiesisMAP Kinase Signaling SystemAntigens, CD34Cell Cycle CheckpointsCell Cycle ProteinsCell ProliferationCells, CulturedDNA-Binding ProteinsErythrocytesErythroid CellsErythroid Precursor CellsErythropoietinGene Knockdown TechniquesGranulocytesHumansOncogene ProteinsAntigens, CD34Cell Cycle ProteinsDNA-Binding ProteinsErythropoietinMFHAS1 protein, humanOncogene Proteinsraf KinasesRNA, MessengerSon of Sevenless Proteins

Identifiers

PMID23327923
PMCPMC3630834
OpenAlexW2167642153

What OpenQuestion holds

Textmetadata
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.