Haplotype CGC from XPD, hOGG1 and ITGA2 polymorphisms increases the risk of nasopharyngeal carcinoma in Malaysia

Autor: Yoke-Yeow Yap, Pei Pei Chong, Hejar Abdul Rahman, Siew Ying Crystale Lim, Eng-Zhuan Ban, Munn-Sann Lye
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Male
Linkage disequilibrium
Integrins
Heredity
Integrin alpha2
lcsh:Medicine
Artificial Gene Amplification and Extension
Restriction Fragment Mapping
medicine.disease_cause
Polymerase Chain Reaction
Linkage Disequilibrium
DNA Glycosylases
Habits
0302 clinical medicine
Gene Frequency
Risk Factors
Genotype
Medicine and Health Sciences
Smoking Habits
lcsh:Science
Genetics
Multidisciplinary
Nasopharyngeal Carcinoma
Alcohol Consumption
Middle Aged
Extracellular Matrix
Genetic Mapping
Oncology
030220 oncology & carcinogenesis
Female
Restriction fragment length polymorphism
Cellular Structures and Organelles
Research Article
Restriction Fragment Length Polymorphism Analysis
Variant Genotypes
Biology
Research and Analysis Methods
Carcinomas
Polymorphism
Single Nucleotide

03 medical and health sciences
medicine
Cell Adhesion
Humans
Genetic Predisposition to Disease
Allele
Molecular Biology Techniques
Molecular Biology
Genetic Association Studies
Nutrition
Xeroderma Pigmentosum Group D Protein
Behavior
lcsh:R
Haplotype
Gene Mapping
Carcinoma
Malaysia
Cancers and Neoplasms
Biology and Life Sciences
Nasopharyngeal Neoplasms
Cell Biology
medicine.disease
Diet
030104 developmental biology
Nasopharyngeal carcinoma
Haplotypes
Cancer research
lcsh:Q
Carcinogenesis
Nucleotide excision repair
Zdroj: PLoS ONE
PLoS ONE, Vol 12, Iss 11, p e0187200 (2017)
ISSN: 1932-6203
Popis: BACKGROUND:8-oxoG, a common DNA lesion resulting from reactive oxygen species (ROS), has been shown to be associated with cancer initiation. hOGG1 DNA glycosylase is the primary enzyme responsible for excision of 8-oxoG through base excision repair (BER). Integrins are members of a family of cell surface receptors that mediate the cell-cell and extracellular matrix (ECM) interactions. Integrins are involved in almost every aspect of carcinogenesis, from cell differentiation, cell proliferation, metastasis to angiogenesis. Loss of ITGA2 expression was associated with enhanced tumor intravasation and metastasis of breast and colon cancer. XPD gene encodes DNA helicase enzyme that is involved in nucleotide excision repair (NER). It is shown in previous research that XPD homozygous wildtype Lys/Lys genotype was associated with higher odds of NPC. METHODS:We conducted a 1 to N case-control study involving 300 nasopharyngeal carcinoma (NPC) cases and 533 controls matched by age, gender and ethnicity to investigate the effect of hOGG1 Ser326Cys, ITGA2 C807T and XPD Lys751Gln polymorphisms on NPC risk. Linkage disequilibrium and haplotype analysis were conducted to explore the association of allele combinations with NPC risk. Restriction fragment length polymorphism (RFLP-PCR) was used for DNA genotyping. RESULTS:No significant association was observed between hOGG1 Ser326Cys and ITGA2 C807T polymorphisms with NPC risk after adjustment for age, gender, ethnicity, cigarette smoking, alcohol and salted fish consumption. Lys/Lys genotype of XPD Lys751Gln polymorphism was associated with increased NPC risk (OR = 1.60, 95% CI = 1.06-2.43). Subjects with history of smoking (OR = 1.81, 95% CI = 1.26-2.60), and salted fish consumption before age of 10 (OR = 1.77, 95% CI = 1.30-2.42) were observed to have increased odds of NPC. The odds of developing NPC of CGC haplotype was significantly higher compared to reference AGC haplotype (OR = 2.20, 95% CI = 1.06-4.58). CONCLUSION:The allele combination of CGC from hOGG1, ITGA2 and XPD polymorphisms was significantly associated with increased odds of NPC.
Databáze: OpenAIRE