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microRNAs are potentially regulating the survivin gene in PBMCs from systemic sclerosis patients.
Ebrahimiyan, Hamidreza; Gharibdoost, Farhad; Aslani, Saeed; Kavosi, Hoda; Farsad, Faraneh; Jamshidi, Ahmadreza; Mahmoudi, Mahdi.
Afiliação
  • Ebrahimiyan H; Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Gharibdoost F; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Aslani S; Rheumatology Expert Group (REG), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
  • Kavosi H; Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Farsad F; Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Jamshidi A; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Mahmoudi M; Rheumatology Expert Group (REG), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Mod Rheumatol ; 30(5): 862-869, 2020 Sep.
Article em En | MEDLINE | ID: mdl-31441344
ABSTRACT

Background:

Survivin is an important anti-apoptotic protein and is involved in increasing auto-reactivity during the autoimmune diseases like systemic sclerosis (SSc).

Aims:

In the current study, we investigate the expression level of total survivin (survivin-TS) and its three important variants alongside with evaluation of the expression level of important microRNAs (miRNAs) that are involved in survivin expression regulation.

Methods:

Peripheral blood mononuclear cells (PBMCs) were isolated from 50 healthy controls, 25 diffuse cutaneous SSc (DcSSc), and 25 limited cutaneous SSc (LcSSc) patients. RNA was extracted and single-strand cDNA was synthesized. Quantitative real-time PCR was used to evaluate the expression level of survivin-TS and its variants as well the miRNAs.

Results:

Overexpression of survivin-2B and downregulation of survivin wild-type (survivin-WT) were found in total-SSc patients; however, expression level of survivin-TS had no significant difference. The expression levels of miR-335-5p, miR-485-5p, miR-16-5p, miR-150-5p, miR-34a-5p, miR-218-5p and miR-708-5p were higher in total-SSc patients. Significantly negative correlations were found between transcript levels of miR-150-5p, miR-16-5p, and miR-485-5p with survivin-TS mRNA expression.

Conclusion:

Survivin variants had altered expression in total-SSc patients. In addition, miRNAs might potentially and negatively regulate the survivin-TS expression. Altered expression of survivin, regulated by miRNAs, may result in apoptosis resistance and auto-reactivity in lymphocytes from patients and have important roles in SSc pathogenicity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / MicroRNAs / Survivina Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / MicroRNAs / Survivina Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article