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Toll-Like Receptor 4, 2, and Interleukin 1 Receptor Associated Kinase4: Possible Diagnostic Biomarkers in Myelodysplastic Syndrome Patients
Myelodysplastic syndrome (MDS) is a clonal hematologic disorder that requires the integration of morphologic, cytogenetic, hematologic, and clinical findings for a successful diagnosis. Trying to find ancillary tests such as biomarkers improve the diagnosis process. Several studies showed that a dis...
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Published in: | Advanced biomedical research 2024-01, Vol.13 (1), p.17-17 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Myelodysplastic syndrome (MDS) is a clonal hematologic disorder that requires the integration of morphologic, cytogenetic, hematologic, and clinical findings for a successful diagnosis. Trying to find ancillary tests such as biomarkers improve the diagnosis process. Several studies showed that a disordered immune system is associated with MDS. The chronic activated innate immune system, particularly the Toll-like receptors (TLRs) pathway could be involved in the induction of the inflammation.
In the present study, we investigated the expression of
, and
in bone marrow (BM) of MDS patients, the leukemia group, and the healthy group. For this purpose, we assessed the expression of
, and
by real time-PCR.
In line with new findings, we demonstrated that the expression of
, and
significantly increased in MDS BM compared with the healthy group. Moreover,
expression raised significantly in MDS patients compared with other studied hematologic neoplasms. Also, the expression levels of
and
significantly increased in MDS in comparison to some studied non-MDS malignancies (
˂ 0.05). Receiver operating characteristics (ROC) analysis and area under the curve (AUC) suggested that the expression of
, and
(AUC = 0.702, AUC = 0.75, and AUC = 0.682, respectively) had acceptable diagnostic values to identify MDS from the other understudied leukemias.
Overall, the expression of
, and
could be potential biomarkers for discriminating MDS from some hematologic disorders. |
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ISSN: | 2277-9175 2277-9175 |
DOI: | 10.4103/abr.abr_67_23 |