The Impact of IL-6 and IL-10 Gene Polymorphisms in Diffuse Large B-Cell Lymphoma Risk and Overall Survival in an Arab Population: A Case-Control Study.

Arab population IL-10 IL-6 diffuse large B-cell lymphoma single nucleotide polymorphism

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
07 Feb 2020
Historique:
received: 03 12 2019
revised: 10 01 2020
accepted: 05 02 2020
entrez: 13 2 2020
pubmed: 13 2 2020
medline: 13 2 2020
Statut: epublish

Résumé

B-cell lymphomas can be classified as Hodgkin and non-Hodgkin lymphomas. Diffuse large B-cell lymphoma (DLBCL) is the most common non-Hodgkin Lymphoma (NHL). The incidence of NHL is variable and affected by age, gender, racial, and geographic factors. There is strong evidence that the immune-regulatory cytokines have a major role in hematologic malignancies. In this study, we analyzed the relationship between seven single nucleotide polymorphisms (SNPs) in two selected cytokines (IL-6 rs1800795G > C, rs1800796G > C, rs1800797G > A, IL-10 rs1800871G > A, rs1800872G > T, rs1800890A > T, rs1800896T > C) and the risk and overall survival of DLBCL patients in a Jordanian Arab population. One hundred and twenty-five DLBCL patients diagnosed at King Abdullah University Hospital (KAUH) from the period 2013-2018 and 238 matched healthy controls were included in the study. Genomic DNA was extracted from formalin-fixed paraffin-embedded tissues. Genotyping of the genetic polymorphisms was conducted using a sequencing protocol. Our study showed no significant differences in the distribution of all studied polymorphisms of DLBCL between patients and controls. The IL-6 rs1800797 was the only SNP to show significant survival results, DLBCL subjects with the codominant model (GG/AG/AA) genotypes and recessive model (AA genotype in comparison with the combined GG/GA genotype) had worse overall survival (

Identifiants

pubmed: 32046104
pii: cancers12020382
doi: 10.3390/cancers12020382
pmc: PMC7072608
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Jordan University of Science and Technology
ID : 20170225

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Auteurs

Sohaib M Al-Khatib (SM)

Department of Pathology and Laboratory Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.

Nour Abdo (N)

Department of Public Health, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.

Laith N Al-Eitan (LN)

Department of Biotechnology and Genetic Engineering, Faculty of Science and Arts, Jordan University of Science and Technology, Irbid 22110, Jordan.

Abdel-Hameed Al-Mistarehi (AH)

Department of Family Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.

Deeb Jamil Zahran (DJ)

Department of Internal Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.

Tariq Zuheir Kewan (TZ)

Department of Internal Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.
Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH 44109, USA.

Classifications MeSH