Author/Authors :
Zargar Balajam, Narges Department of Clinical Biochemistry - Isfahan Pharmaceutical Sciences Research Center - School of Pharmacy - Isfahan University of Medical Sciences, Isfahan, Iran , Shabani, Mahdi Department of Immunology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Aghaei, Mahmoud Department of Clinical Biochemistry - Isfahan Pharmaceutical Sciences Research Center - School of Pharmacy - Isfahan University of Medical Sciences, Isfahan, Iran , Haghighi, Mansoureh Department of Clinical Biochemistry - Isfahan Pharmaceutical Sciences Research Center - School of Pharmacy - Isfahan University of Medical Sciences, Isfahan, Iran , Kompani, Farzad Department of Hematology and Oncology - Children’s Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Background: Acute lymphoblastic leukemia (ALL) is a malignancy with aggressive tumors of immature lymphocytes. T‑cell
immunoglobulin and mucin‑domain 3 (TIM‑3) is a Type I transmembrane glycoprotein which is involved in cell proliferation. The
objective of this research is to determine the TIM‑3 expression in peripheral blood (PB) and bone marrow (BM) of 80 samples of
normal and ALL patients. Materials and Methods: The amount of mRNA and protein of TIM‑3 measured in the BM and PB the
mononuclear layer of samples by real‑time polymerase chain reaction and Western blotting. Results: Our findings indicated that
relative mRNA expression of TIM‑3 in PB and BM of the mononuclear layer of ALL patients was 1.7 and 5 times higher than normals,
respectively. We also reported that the protein level of TIM‑3 in mononuclear cells of ALL patients was 3.2‑fold in BM and two‑fold
in PB more than normals. Conclusion: In conclusion, this study shows that TIM‑3 increases in ALL patients, thus the expression
of TIM‑3 in tumor cells may be considered as a potential predictive factor in ALL patients, which needs to be explored in future.
Keywords :
T‑cell immunoglobulin and mucin‑domain 3 , real‑time polymerase chain reaction , precursor cell lymphoblastic leukemia‑lymphoma , Gene expression profiling