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Single-Nucleotide Polymorphisms of FAS and FASL Genes and Risk of Idiopathic Aplastic Anemia.
Rehman, Sadia; Saba, Nusrat; Naz, Madiha; Ahmed, Parvez; Munir, Saeeda; Sajjad, Sumaira; Tabassum, Sobia; Naseem, Lubna.
Afiliación
  • Rehman S; a Institute of Biomedical and Genetic Engineering Islamabad , Pakistan.
  • Saba N; a Institute of Biomedical and Genetic Engineering Islamabad , Pakistan.
  • Naz M; b Islamic International University Islamabad , Pakistan.
  • Ahmed P; c Armed forces Bone Marrow Transplantation Centre Rawalpindi , Pakistan.
  • Munir S; a Institute of Biomedical and Genetic Engineering Islamabad , Pakistan.
  • Sajjad S; a Institute of Biomedical and Genetic Engineering Islamabad , Pakistan.
  • Tabassum S; b Islamic International University Islamabad , Pakistan.
  • Naseem L; d Pakistan Institute of Medical Sciences Islamabad , Pakistan.
Immunol Invest ; 47(5): 484-491, 2018 Jul.
Article en En | MEDLINE | ID: mdl-29611722
FAS/FASL signaling system plays a vital role in the regulation of apoptosis, envisaged as a death process required for immune surveillance to prevent autoimmunity and tumorigenesis along with several other biological activities. Several single-nucleotide polymorphisms (SNPs) of FAS/FASL system can result in aberrant apoptosis, which can cause different cancers and autoimmune diseases. Aplastic anemia (AA) is an autoimmune dysfunction characterized by peripheral blood pancytopenia associated with hypoplasia of bone marrow. The aim of this study was to screen Pakistani AA patients and controls for two Fas SNPs rs2234767 and rs1800682 and two FASLG SNPs rs763110 and rs5030772. Genotyping of 392 DNA samples was done by Tetra-ARMS polymerase chain reaction. Genotypic frequencies of Fas rs1800682 and FASLG rs5030772 showed significance difference in their distribution in both controls and patients, while Fas rs2234767 and FASLG rs763110 SNPs had no such difference. Carriers of rs1800682 AG+GG had a very odd ratio of 4.63, with 95% confidence interval (CI) of 3.01-7.11, while individuals with FASLG rs5030772 AG+GG were more common in controls than patients with OR 0.53 and 95% CI of 0.34-0.83. Cumulative effects of these SNPs were analyzed, and they showed almost similar trends; however, Fas rs2234767 and FASLG rs763110 genotypes in combination with Fas rs1800682 and FASLG rs5030772 demonstrated significant association. This study provided information that endorsed the involvement of FAS/FASL system SNPs in the pathogenesis of AA; further studies should be designed to understand the exact role of SNPs that can help in early diagnosis and treatment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptor fas / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Proteína Ligando Fas / Estudios de Asociación Genética / Anemia Aplásica Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Immunol Invest Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Pakistán Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptor fas / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Proteína Ligando Fas / Estudios de Asociación Genética / Anemia Aplásica Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Immunol Invest Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Pakistán Pais de publicación: Reino Unido