Evidence map›Paper›PMID 27275226›Full record

ArticleOpen access Macedonian journal of medical sciences2015

Detection of BCR/ABL Translocation in Bone Marrow Derived Mesenchymal Stem Cells in Egyptian CML Patients.

Taghrid Mohamed Gaafar, Inas Ismail Raafat, Azza Ahmed Aly, Nagwa Abd El-Ghaffar Mohamed, Reem Jan Farid, Neveen Ezzat Saad, Rabab El-Hawary, Naglaa Mostafaa, Mirhan Mohamed Ahmed

Open access · diamondAbstract read
In one paragraph

Article in Open access Macedonian journal of medical sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 97% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
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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.

Taghrid Mohamed GaafarDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Inas Ismail RaafatDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Azza Ahmed AlyDepartment of Clinical and Chemical Pathology, National Research Center, Egypt.
Nagwa Abd El-Ghaffar MohamedDepartment of Clinical and Chemical Pathology, National Research Center, Egypt.
Reem Jan FaridDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Neveen Ezzat SaadDepartment of Clinical and Chemical Pathology, National Research Center, Egypt.
Rabab El-HawaryDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Naglaa MostafaaDepartment of Clinical and Chemical Pathology, National Cancer Institute, Cairo, Egypt.
Mirhan Mohamed AhmedDepartment of Clinical and Chemical Pathology, National Research Center, Egypt.
Cairo University · EGNational Water Research Center · EGNational Cancer Institute · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic myeloid leukemia (CML) is a clonal myeloproliferative disorder of hematopoietic stem cells. It is characterized at the cytogenetic level by Philadelphia (ph) chromosome and at the molecular level by the BCR/ABL gene rearrangement. Bone marrow derived mesenchymal stem cells (MSCs) are pluripotent stem cells that can differentiate into several mesenchymal tissues.

aimTo observe the biological characteristics of MSCS from CML patients and to determine whether MSCs harbor the abnormal BCR/ABL translocation similar to CML bone marrow cells. SUBJECTS AND

methodsCharacterized MSCs were isolated from 12 newly diagnosed Philadelphia positive untreated CML patients.

resultsMSCs can be readily isolated from CML marrow and exhibit major expansion. Flow cytometry analysis revealed the typical MSC phenotype. Moreover; MSCs do not harbor the BCR/ABL translocation confirmed by karyotype and real time PCR.

conclusionMSCs from CML patients express the typical MSC phenotype; and do not express the BCR/ABL gene. Since; MSCs are able to support engraftment of hematopoietic stem cells in stem cell transplantation(SCT) as well as suppress alloreactive T cells causing graft versus -host disease, this current study provides evidence that in a SCT setting of CML patients, autologous MSCs could be a source of stem cell support in future cell therapy applications.

Indexed as

Chronic myeloid leukemiamesenchymal stem cellPhiladelphia chromosome

Identifiers

PMID27275226
PMCPMC4877858
OpenAlexW1802161309

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.