Evidence map›Paper›PMID 29141658›Full record

ArticleStem cell research & therapy2017

Thioredoxin mitigates radiation-induced hematopoietic stem cell injury in mice.

Pasupathi Sundaramoorthy, Qinhong Wang, Zhihong Zheng, Yiqun Jiao, Benny J Chen, Phuong L Doan, Nelson J Chao, Yubin Kang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  8. Review
  9. Review
  10. Targets for protection and mitigation of radiation injury.Cellular and molecular life sciences : CMLS · 2020
    Review
  11. Protective Effects of Biscoclaurine Alkaloids on Leukopenia Induced byEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  12. Article
  13. Article
  14. Article
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

8 authors at 1 institution in 2 countries.

Pasupathi SundaramoorthyDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Qinhong WangDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Zhihong ZhengDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Yiqun JiaoDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Benny J ChenDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Phuong L DoanDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Nelson J ChaoDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA.
Yubin KangDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, DUMC 3961, 2400 Pratt Street, Suite 9000, Durham, NC, 27710, USA. yubin.kang@duke.edu.
Duke Medical Center · US

Funding

Sample Engineering CoreU19AI067773 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FORNACE, ALBERT J · 2005 to 2024
$105.4M
Clinical Trial of ABC294640 in Patients with Refractory Multiple MyelomaR44CA199767 · NCI · APOGEE BIOTECHNOLOGY CORPORATION · PI SMITH, CHARLES D · 2015 to 2017
$2.0M
Targeting sphingosine kinase 2 for the treatment of multiple myelomaR01CA197792 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2015 to 2019
$1.8M
Plerixafor for allogeneic hematopoietic stem cell transplantationK08HL103780 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KANG, YUBIN · 2011 to 2015
$649k
Role of ErbB receptor signaling in regulating normal and leukemic stem cell fateK08CA184552 · NCI · DUKE UNIVERSITY · PI DOAN, PHUONG LINH · 2014 to 2018
$639k
National Heart, Lung, and Blood Institute (US) K08HL103780, NCI R01CA197792National Institute of Allergy and Infectious Diseases U19AI067773NCI NIH HHS K08 CA184552NCI NIH HHS R01 CA197792NCI NIH HHS R44 CA199767NHLBI NIH HHS K08 HL103780NIAID NIH HHS U19 AI067773
6 · The paper itself

Abstract

backgroundRadiation exposure poses a significant threat to public health. Hematopoietic injury is one of the major manifestations of acute radiation sickness. Protection and/or mitigation of hematopoietic stem cells (HSCs) from radiation injury is an important goal in the development of medical countermeasure agents (MCM). We recently identified thioredoxin (TXN) as a novel molecule that has marked protective and proliferative effects on HSCs. In the current study, we investigated the effectiveness of TXN in rescuing mice from a lethal dose of total body radiation (TBI) and in enhancing hematopoietic reconstitution following a lethal dose of irradiation.

methodsWe used in-vivo and in-vitro methods to understand the biological and molecular mechanisms of TXN on radiation mitigation. BABL/c mice were used for the survival study and a flow cytometer was used to quantify the HSC population and cell senescence. A hematology analyzer was used for the peripheral blood cell count, including white blood cells (WBCs), red blood cells (RBCs), hemoglobin, and platelets. Colony forming unit (CFU) assay was used to study the colongenic function of HSCs. Hematoxylin and eosin staining was used to determine the bone marrow cellularity. Senescence-associated β-galactosidase assay was used for cell senescence. Western blot analysis was used to evaluate the DNA damage and senescence protein expression. Immunofluorescence staining was used to measure the expression of γ-H2AX foci for DNA damage.

resultsWe found that administration of TXN 24 h following irradiation significantly mitigates BALB/c mice from TBI-induced death: 70% of TXN-treated mice survived, whereas only 25% of saline-treated mice survived. TXN administration led to enhanced recovery of peripheral blood cell counts, bone marrow cellularity, and HSC population as measured by c-Kit

conclusionsAdministration of TXN 24 h following irradiation mitigates radiation-induced lethality. To the best of our knowledge, this is the first report demonstrating that TXN reduces radiation-induced lethality. TXN shows potential utility in the mitigation of radiation-induced hematopoietic injury.

Indexed as

Whole-Body IrradiationAnimalsAntigens, LyBiomarkersBlood Cell CountBone MarrowCell LineCellular SenescenceColony-Forming Units AssayCyclin-Dependent Kinase Inhibitor p16FemaleFibroblastsGene ExpressionHematocritHematopoiesisHematopoietic Stem CellsAntigens, LyBiomarkersCyclin-Dependent Kinase Inhibitor p16Ly6a protein, mouseMembrane Proteinsp38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-kitRadiation-Protective AgentsRecombinant ProteinsThioredoxinsTXN protein, humanHematopoietic stem cellsMitigationRadiation exposureSenescenceThioredoxin

Identifiers

PMID29141658
PMCPMC5688691
OpenAlexW2769223713

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.