Association of Variants in IL6-Related Genes with Lung Cancer Risk in Moroccan Population.


Journal

Lung
ISSN: 1432-1750
Titre abrégé: Lung
Pays: United States
ID NLM: 7701875

Informations de publication

Date de publication:
10 2019
Historique:
received: 15 04 2019
accepted: 08 08 2019
pubmed: 31 8 2019
medline: 1 5 2020
entrez: 31 8 2019
Statut: ppublish

Résumé

Lung cancer is known to be a complex multifactorial disease, involving both genetic and environmental factors. The study of the different signaling pathways and the identification of the genes involved, will contribute to further understanding the pathogenesis of the disease, thus allowing the development of appropriate targeted treatments. Recently, the link between cancer and inflammation has become more evident and inflammation has been proposed as the seventh hallmark of cancer. Previous studies have suggested that key cytokines involved in inflammation may have an important role in the etiology of lung cancer. The aim of this study was to investigate whether common variants in inflammation-related genes: IL-6, IL6-R, and IL6-ST, influence lung cancer risk in Moroccan population. Single nucleotide polymorphisms (SNPs) in IL-6, IL6-R, and IL6-ST genes were assessed in 120 controls and 120 patients with confirmed lung cancer diagnosis. Genotyping analysis was performed with the TaqMan® allelic discrimination technology. The results were analyzed using SPSS 24.0 software. Among the studied SNPs, we found a significant association for the IL-6 (rs2069840) (OR = 1.63; 95% confidence interval 1.08-2.47; p = 0.01). No significant association was observed for the remaining SNPs of IL-6R (rs2228145) and IL-6ST (rs2228044) genes. Our results suggest the IL-6 (rs2069840) polymorphism may influence the occurrence of lung cancer in Moroccan patients.

Identifiants

pubmed: 31468132
doi: 10.1007/s00408-019-00261-0
pii: 10.1007/s00408-019-00261-0
doi:

Substances chimiques

IL6 protein, human 0
IL6R protein, human 0
IL6ST protein, human 0
Interleukin-6 0
Receptors, Interleukin-6 0
Cytokine Receptor gp130 133483-10-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

601-608

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Auteurs

Houda Kaanane (H)

Laboratory of Genetics and Molecular Pathology, Faculty of Medicine and Pharmacy of Casablanca, University Hassan II, 20250, Casablanca, Morocco. kaanane.h@gmail.com.

Nezha Senhaji (N)

Laboratory of Genetics and Molecular Pathology, Faculty of Medicine and Pharmacy of Casablanca, University Hassan II, 20250, Casablanca, Morocco.

Hind Berradi (H)

Laboratory of Genetics and Molecular Pathology, Faculty of Medicine and Pharmacy of Casablanca, University Hassan II, 20250, Casablanca, Morocco.

Nadia Benchakroun (N)

Oncology Department, Mohammed VI Center for Cancer Treatment, CHU Ibn Rochd, 20250, Casablanca, Morocco.

Abdellatif Benider (A)

Oncology Department, Mohammed VI Center for Cancer Treatment, CHU Ibn Rochd, 20250, Casablanca, Morocco.

Mehdi Karkouri (M)

Anathomo-Pathology Department, CHU Ibn Rochd, 20250, Casablanca, Morocco.

Hicham El Attar (H)

Annasr Pathology Center, El Jadida, Morocco.
IGOT CASA: Inter Group of Thoracic Oncology, CHU Ibn Rochd, 20250, Casablanca, Morocco.

Meriem Khyatti (M)

Oncovirology Laboratory, Institut Pasteur du Maroc, 20250, Casablanca, Morocco.

Sellama Nadifi (S)

Laboratory of Genetics and Molecular Pathology, Faculty of Medicine and Pharmacy of Casablanca, University Hassan II, 20250, Casablanca, Morocco.

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Classifications MeSH