Expression Pattern and Prognostic Significance of the Long Non-Coding RNA Metastasis-Associated Lung Adenocarcinoma Transcript 1 in Chronic Lymphocytic Leukemia
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Published:2024-01-11
Issue:2
Volume:25
Page:922
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ISSN:1422-0067
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Container-title:International Journal of Molecular Sciences
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language:en
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Short-container-title:IJMS
Author:
Tomic Vujovic Kristina1ORCID, Ugrin Milena2, Tosic Natasa2ORCID, Vukovic Vojin1, Marjanovic Irena2, Kostic Tatjana2, Stankovic Sanja34ORCID, Otasevic Vladimir1ORCID, Sarac Sofija1, Antic Darko15ORCID, Pavlovic Sonja2, Karan-Djurasevic Teodora2ORCID
Affiliation:
1. Clinic for Hematology, University Clinical Center of Serbia, 11000 Belgrade, Serbia 2. Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, 11042 Belgrade, Serbia 3. Center for Medical Biochemistry, University Clinical Center of Serbia, 11000 Belgrade, Serbia 4. Department of Biochemistry, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia 5. School of Medicine, University of Belgrade, 11000 Belgrade, Serbia
Abstract
Dysregulated expression of the long non-coding RNA MALAT1 has been implicated in the pathogenesis and progression of a variety of cancers, including hematological malignancies, but it has been poorly investigated in chronic lymphocytic leukemia (CLL). In this study, the expression of MALAT1 was measured using a quantitative reverse-transcriptase polymerase chain reaction in the peripheral blood mononuclear cells of 114 unselected, newly diagnosed CLL patients in order to analyze its association with clinical, laboratory, and molecular patients’ characteristics at diagnosis, as well as its prognostic relevance. MALAT1 was found to be upregulated in CLL patients in comparison to healthy controls, and expression levels were not related to age, leukocyte, lymphocyte and platelet count, serum β2-microglobulin, and IGHV somatic hypermutational status. On the other hand, high MALAT1 expression was associated with several favorable prognostic markers (high hemoglobin, low serum lactate dehydrogenase, earlier clinical stages, CD38-negative status), but also with unfavorable cytogenetics. Furthermore, an association between high MALAT1 levels and longer time to first treatment and overall survival in IGHV-unmutated CLL subtype was observed. In summary, our results imply that high MALAT1 expression at diagnosis may be a predictor of better prognosis and point to MALAT1 expression profiling as a candidate biomarker potentially useful in clinical practice.
Funder
Ministry of Education, Science and Technological Development, Republic of Serbia
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