PMID- 31522447 OWN - NLM STAT- MEDLINE DCOM- 20200205 LR - 20200205 IS - 1735-5249 (Electronic) IS - 1735-1502 (Linking) VI - 18 IP - 4 DP - 2019 Aug 17 TI - Genetic Polymorphisms of CXCL8 (-251) Are Associated with the Susceptibility of Helicobacter pylori Infection Increased the Risk of Inflammation and Gastric Cancer in Thai Gastroduodenal Patients. PG - 393-401 LID - 10.18502/ijaai.v18i4.1417 [doi] AB - CXC Chemokine Ligand 8 (CXCL8) plays an important role in gastric inflammation and in the progression of gastric cancer induced by Helicobacter pylori (H. pylori) infection. The association of CXCL8, CXC Chemokine Receptor 1 (CXCR1), and CXC Chemokine Receptor 2 (CXCR2) polymorphisms with H. pylori infection and gastric cancer progression needs to be investigated in a population within an enigma area consisting of multiple ethnicities, such as Thailand. To analyze the relative risk of H. pylori infection and gastric cancer among Thai gastroduodenal patients, gene polymorphisms in CXCL8 (promoter region -251) and in CXCR1 and CXCR2 (receptors for CXCL8) were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and allele specific-PCR (AS-PCR). We also determined the presence of cytotoxin-associated gene A (cagA) in Thai patients with H. pylori infection. Correlation between the CXCL8 (-251) polymorphism and CXCL8 gene expression was evaluated by quantitative reverse transcriptase-PCR (qRT-PCR). We found a significant association between the T/A and A/A genotypes of CXCL8 (-251) with H. pylori infection. However, no significant correlation was found between the CXCR1 (+2607) and CXCR2 (+1208) gene polymorphisms with H. pylori infection among Thai gastroduodenal subjects. Within the H. pylori-infected group of Thai gastroduodenal patients, no significant differences in cagA were observed. In addition, the A/A genotype of CXCL8 (-251) significantly correlated with the risk of gastric cancer and correlated with higher CXCL8 gene expression levels in Thai gastroduodenal patients. These results suggest that CXCL8 (-251) polymorphisms are associated with H. pylori infection, an increased risk of stronger inflammatory responses, and gastric cancer in Thai gastroduodenal patients. FAU - Boonyanugomol, Wongwarut AU - Boonyanugomol W AD - Department of Sciences and Liberal Arts, Mahidol University, Amnat Charoen Campus, Amnat Charoen, Thailand. wongwarut.boo@mahidol.ac.th. FAU - Rukseree, Kamolchanok AU - Rukseree K AD - Department of Sciences and Liberal Arts, Mahidol University, Amnat Charoen Campus, Amnat Charoen, Thailand. Kamolchanok.ruk@mahidol.edu. FAU - Kongkasame, Worrarat AU - Kongkasame W AD - Unit of Endoscopy Medicine, Suppasittiprasong Hospital, Ubon Ratchathani, Thailand. Worrarat-eab@hotmail.com. FAU - Palittapongarnpim, Prasit AU - Palittapongarnpim P AD - Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand. Prasit.pal@mahidol.ac.th. FAU - Baik, Seung-Chul AU - Baik SC AD - Department of Microbiology, Gyeongsang National Institute of Health Sciences, School of Medicine, Gyeongsang National University, Jinju, Republic of Korea. scbaik@gnu.ac.kr. FAU - Manwong, Mereerat AU - Manwong M AD - College of Medicine and Public Health, Ubon Ratchathani University, Ubon Ratchathani, Thailand. Mereerat_s@hotmail.com. LA - eng PT - Journal Article DEP - 20190817 PL - Iran TA - Iran J Allergy Asthma Immunol JT - Iranian journal of allergy, asthma, and immunology JID - 101146178 RN - 0 (Interleukin-8) SB - IM MH - Alleles MH - Disease Susceptibility MH - Female MH - Gastritis/complications/epidemiology/*etiology MH - Gene Frequency MH - Genotype MH - Helicobacter Infections/*complications/microbiology MH - *Helicobacter pylori MH - Humans MH - Interleukin-8/*genetics MH - Male MH - *Polymorphism, Genetic MH - Population Surveillance MH - Stomach Neoplasms/epidemiology/*etiology MH - Thailand/epidemiology OTO - NOTNLM OT - CXC chemokine ligand 8 OT - CXC chemokine receptor 1 OT - CXC chemokine receptor 2 OT - Gene polymorphism OT - Helicobacter pylori OT - Thai EDAT- 2019/09/16 06:00 MHDA- 2020/02/06 06:00 CRDT- 2019/09/16 06:00 PHST- 2018/12/09 00:00 [received] PHST- 2019/04/16 00:00 [accepted] PHST- 2019/09/16 06:00 [entrez] PHST- 2019/09/16 06:00 [pubmed] PHST- 2020/02/06 06:00 [medline] AID - 10.18502/ijaai.v18i4.1417 [doi] PST - epublish SO - Iran J Allergy Asthma Immunol. 2019 Aug 17;18(4):393-401. doi: 10.18502/ijaai.v18i4.1417.