Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Altered Expression of Malat 1 Lncrna in Chronic Lymphocytic Leukemia Patients, Correlation With Cytogenetic Findings Publisher



Ahmadi A1 ; Kaviani S1 ; Yaghmaie M2, 3, 4 ; Pashaiefar H2, 3, 4 ; Ahmadvand M2, 3, 4 ; Jalili M2, 3, 4 ; Alimoghaddam K2, 3, 4 ; Eslamijouybari M5 ; Ghavamzadeh A2, 3, 4
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University, P.O. Box: 14115-331, Tehran, Iran
  2. 2. Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, P.O. Box: 1411713135, Tehran, Iran
  3. 3. Cell Therapy and Hematopoietic Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Hematologic Malignancies Research Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Comprehensive Cancer Research Center, Mazandaran University of Medical Science, Sari, Iran

Source: Blood Research Published:2018


Abstract

Background: Recent studies have devoted much attention to non-protein-coding transcripts in relation to a wide range of malignancies. MALAT1, a long non-coding RNA, has been reported to be associated with cancer progression and prognosis. Thus, we here determined MALAT1 gene expression in chronic lymphocytic leukemia (CLL), a genetically heterogeneous disease, and explored its possible relationships with cytogenetic abnormalities. Methods: MALAT1 expression level was evaluated using real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) on blood mononuclear cells from 30 non-treated CLL patients and 30 matched healthy controls. Cytogenetic abnormalities were determined in patients by fluorescence in situ hybridization (FISH). Results: MALAT1 expression level was up-regulated in the CLL group compared to healthy controls (P=0.008). Del13q14, followed by Del11q22, were the most prevalent cytogenetic abnormalities. We found no association between the FISH results and MALAT1 expression in patients. Conclusion: Altered expression of MALAT1 is associated with CLL development. Further investigations are required to assess the relationship between this long non-coding RNA and CLL patient survival and prognosis. © 2018 Korean Society of Hematology.