Evidence map›Paper›PMID 25663975›Full record

ArticleInternational journal of clinical and experimental medicine2014

IL1RAP as a surface marker for leukemia stem cells is related to clinical phase of chronic myeloid leukemia patients.

Kai Zhao, Ling-Ling Yin, Dong-Mei Zhao, Bin Pan, Wei Chen, Jiang Cao, Hai Cheng, Zhen-Yu Li, De-Peng Li, Wei Sang and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  15. IL1RAP potentiates multiple oncogenic signaling pathways in AML.The Journal of experimental medicine · 2018
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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

12 authors at 1 institution in 1 country.

Kai ZhaoBlood Diseases Institute, Xuzhou Medical College No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu, China ; Key Laboratory of Bone Marrow Stem Cell No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu Province, China ; Department of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Ling-Ling YinBlood Diseases Institute, Xuzhou Medical College No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Dong-Mei ZhaoBlood Diseases Institute, Xuzhou Medical College No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Bin PanBlood Diseases Institute, Xuzhou Medical College No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu, China ; Key Laboratory of Bone Marrow Stem Cell No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu Province, China ; Department of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Wei ChenDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Jiang CaoDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Hai ChengDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Zhen-Yu LiDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
De-Peng LiDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Wei SangDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Ling-Yu ZengBlood Diseases Institute, Xuzhou Medical College No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu, China ; Key Laboratory of Bone Marrow Stem Cell No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu Province, China ; Department of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Kai-Lin XuBlood Diseases Institute, Xuzhou Medical College No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu, China ; Key Laboratory of Bone Marrow Stem Cell No. 84 West Huaihai Road, Xuzhou 221002, Jiangsu Province, China ; Department of Hematology, The Affiliated Hospital of Xuzhou Medical College No. 99 West Huaihai Road, Xuzhou 221002, Jiangsu, China.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) is a clonal disease from hematopoietic stem cells. Surviving leukemia stem cells (LSCs) and progenitor cells are a potential source for CML relapse and progression. Recent data reported that IL-1 receptor accessory protein (IL1RAP) gene was differentially expressed in CML versus normal stem and progenitor cells. However, whether the level of IL1RAP is associated with clinical phases of CML, and correlations between IL1RAP expression and detections of diagnosis is still unclear. Here we demonstrated that IL1RAP was up-regulated in CD34+ and CD34+CD38- cells which highly enriched with stem cells. Furthermore, IL1RAP expression in CD34+CD38- cells was tightly consistent with the generation of BCR-ABL fusion gene and Philadelphia chromosome. Importantly, we found that the level of IL1RAP increased with disease progression from chronic phase (CP) into accelerated phase (AP) and blast phase (BP), which was investigated not only in new diagnosed CML patients but also in patients treated with tyrosine kinase inhibitors (TKI) and hydroxyurea. Negative correlation was detected between IL1RAP expression and neutrophil (NE), whereas no relation was found in white blood cell (WBC), lymphocyte (LY), red blood cell (RBC), platelet (PLT), age or gender of CML patients. In conclusion, we identified IL1RAP as a surface marker of LSCs may be a potential indicator for CML clinical phases.

Indexed as

Chronic myeloid leukemiaIL-1 receptor accessory proteinleukemia stem cells

Identifiers

PMID25663975
PMCPMC4307422
OpenAlexW23811499

What OpenQuestion holds

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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.