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Pharm Sci. 2021;27(3): 385-392.
doi: 10.34172/PS.2020.84

Scopus ID: 85115270040
  Abstract View: 829
  PDF Download: 580

Research Article

Expression Profile of LncRNAs in Childhood Acute Lymphoblastic Leukemia: A Pilot Study

Zohreh Mousavi 1, Saeid Ghorbian 1* ORCID logo, Azim Rezamand 2, Leyla Roshangar 3, Behboud Jafari 4

1 Department of Molecular Genetics, Ahar Branch, Islamic Azad University, Ahar, Iran.
2 Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
3 Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
4 Department of Microbiology, Ahar Branch, Islamic Azad University, Ahar, Iran.
*Corresponding Author: Email: ghorbian20@gmail.com

Abstract

Background: Childhood acute lymphoblastic leukemia (ALL) explains 26% of pediatricmalignancies and is one of the leading causes of disease-related deaths in children. A novelmolecular class of non-coding genes, long non-coding RNAs (lncRNAs) having over 200nucleotides, have been defined as regulators of different cellular processes including pluripotency,oncogenesis, and transcription. It has been demonstrated that lncRNA transcription profilescan distinguish pre B-cell subtype of ALL accurately and act as early diagnostic and prognosticbiomarkers. Hence, the aim of this pilot study was the prior evaluation of expression profileof several lncRNA candidates including RP11-68I18.10, RP11-624C23.1, RP11-446E9, RP11-137H2.4, and RP11-203E8 in patients with ALL.

Methods: In this study, 80 blood samples were obtained from patients, definitely diagnosed bypathologists with ALL, and from healthy subjects. Total RNA was extracted from blood samples,and cDNA was synthesized. Real-time PCR was applied to determine the expression of lncRNAs.A P-value of 0.010 was considered statistically significant.

Results: Our findings revealed that the expression levels of lncRNAs RP11-624C23.1, RP11-446E9, RP11-137H2.4, RP11-68I18.10, and RP11-203E8 were significantly decreased in ALLsamples compared to those of healthy samples (P<0.0001, P =0.0616, P =0.0292, P<0.0001, andP = 0.0007). Moreover, the relationship between these five lncRNA expression changes and theimmunophenotype in ALL patients was not significant.

Conclusion: The dysregulation of lncRNAs in ALL samples could provide a novel and interestingpossibility for early diagnosis and prognosis, as well as mastering the treatment of ALL.

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Submitted: 22 Aug 2020
Revision: 11 Oct 2020
Accepted: 12 Oct 2020
ePublished: 29 Oct 2020
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