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Common variants in toll-like receptor family genes and risk of gastric cancer: a systematic review and meta-analysis.
Al Othaim, Ayoub; Al-Hawary, Sulieman Ibraheem Shelash; Alsaab, Hashem O; Almalki, Sami G; Najm, Mazin A A; Hjazi, Ahmed; Alsalamy, Ali; Firras Almulla, Abbas; Alizadeh, Hamzeh.
Afiliación
  • Al Othaim A; Department of Medical Laboratories, College of Applied Medical Sciences, Majmaah University, Al-Majmaah, Saudi Arabia.
  • Al-Hawary SIS; Department of Business Administration, Business School, Al al-Bayt University, Mafraq, Jordan.
  • Alsaab HO; Department of Pharmaceutics and Pharmaceutical Technology, Taif University, Taif, Saudi Arabia.
  • Almalki SG; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Majmaah, Saudi Arabia.
  • Najm MAA; Pharmaceutical Chemistry Department, College of Pharmacy, Al-Ayen University, Thi-Qar, Iraq.
  • Hjazi A; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia.
  • Alsalamy A; College of Medical Technology, Imam Ja'afar Al-Sadiq University, Al-Muthanna, Iraq.
  • Firras Almulla A; Medical Laboratory Technology Department, College of Medical Technology, The Islamic University, Najaf, Iraq.
  • Alizadeh H; Genetics Research Center, Department of Genetics and Breeding, The University of Guilan, Rasht, Iran.
Front Genet ; 14: 1280051, 2023.
Article en En | MEDLINE | ID: mdl-38090147
ABSTRACT

Background:

An increasing number of studies have suggested the relationship between single-nucleotide polymorphisms (SNPs) in toll-like receptor (TLR) genes and gastric cancer (GC) susceptibility; however, the available evidence is contradictory. This meta-analysis aimed to comprehensively evaluate whether the SNPs within the TLR family are related to GC development.

Methods:

PubMed, Scopus, and China National Knowledge Infrastructure (CNKI) were systematically searched up to May 2023 to obtain the pertinent publications. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were applied to examine the associations using the random-effects model.

Results:

A total of 45 studies with 25,831 participants (cases 11,308; controls 14,523) examining the relation of 18 different SNPs in the TLR family to GC were analyzed. Variations in TLR-4 rs4986790, TLR-4 rs4986791, TLR-5 rs5744174, and TLR-9 rs187084 were significantly associated with increased risk of GC in different genetic models. No significant association was detected for TLR-2-196 to -174de (Delta22), TLR-2 rs3804100, TLR-4 rs11536889, TLR-4 rs11536878, TLR-4 rs2770150, TLR-4 rs10116253, TLR-4 rs1927911, TLR-4 rs10983755, TLR-4 rs10759932, TLR-4 rs1927914, and TLR-10 rs10004195.

Conclusion:

These findings indicate that variations in TLR-4, TLR-5, and TLR-9 genes were found to be potential risk factors for GC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Systematic_reviews Idioma: En Revista: Front Genet Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Systematic_reviews Idioma: En Revista: Front Genet Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita