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Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings

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 ly...

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Autores principales: Ahmadi, Abdolrahim, Kaviani, Saeid, Yaghmaie, Marjan, Pashaiefar, Hossein, Ahmadvand, Mohammad, Jalili, Mahdi, Alimoghaddam, Kamran, Eslamijouybari, Mohammad, Ghavamzadeh, Ardeshir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300670/
https://www.ncbi.nlm.nih.gov/pubmed/30588470
http://dx.doi.org/10.5045/br.2018.53.4.320
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author Ahmadi, Abdolrahim
Kaviani, Saeid
Yaghmaie, Marjan
Pashaiefar, Hossein
Ahmadvand, Mohammad
Jalili, Mahdi
Alimoghaddam, Kamran
Eslamijouybari, Mohammad
Ghavamzadeh, Ardeshir
author_facet Ahmadi, Abdolrahim
Kaviani, Saeid
Yaghmaie, Marjan
Pashaiefar, Hossein
Ahmadvand, Mohammad
Jalili, Mahdi
Alimoghaddam, Kamran
Eslamijouybari, Mohammad
Ghavamzadeh, Ardeshir
author_sort Ahmadi, Abdolrahim
collection PubMed
description 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.
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spelling pubmed-63006702018-12-26 Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings Ahmadi, Abdolrahim Kaviani, Saeid Yaghmaie, Marjan Pashaiefar, Hossein Ahmadvand, Mohammad Jalili, Mahdi Alimoghaddam, Kamran Eslamijouybari, Mohammad Ghavamzadeh, Ardeshir Blood Res Original Article 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. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2018-12 2018-12-17 /pmc/articles/PMC6300670/ /pubmed/30588470 http://dx.doi.org/10.5045/br.2018.53.4.320 Text en © 2018 Korean Society of Hematology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ahmadi, Abdolrahim
Kaviani, Saeid
Yaghmaie, Marjan
Pashaiefar, Hossein
Ahmadvand, Mohammad
Jalili, Mahdi
Alimoghaddam, Kamran
Eslamijouybari, Mohammad
Ghavamzadeh, Ardeshir
Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
title Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
title_full Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
title_fullStr Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
title_full_unstemmed Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
title_short Altered expression of MALAT1 lncRNA in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
title_sort altered expression of malat1 lncrna in chronic lymphocytic leukemia patients, correlation with cytogenetic findings
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300670/
https://www.ncbi.nlm.nih.gov/pubmed/30588470
http://dx.doi.org/10.5045/br.2018.53.4.320
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