Study on the relationship between glutathione S-transferase M1, T1 genotypes and Kazak esophageal cancer
Xiaomei Lu
Abstract
Xiaomei Lu
Abstract
Objective To explore the association between genetic polymorphisms of glutathione S-transferase (GST) M1 and T1 and susceptibility to Kazak population esophageal cancer (EC). Methods A polymerase chain reaction method was used to detect absence of the GSTM1 and GSTT1 genes in genomic DNA in a high-risk ethnic, Xinjiang, China. Results The frequency of the GSTM1-null genotype in cancer cases (41.47%) was not significantly different from that in controls ( 34.15%). Similarly, no statistically significant differences were observed in the frequency of GSTT1-null genotype in cancer cases (48.78%) compared with control (51.22%). However, the frequency of GSTM1 null alleles genotypes in cases with well-differentiated cancer ( 15.38%) showed a significant decrease compared with that in poor-differentiated cancer ( 53.57%) (P0.05). Conclusions GSTM1-null genotypes may act as risk factor in the development of poor-differentiated esophageal cancer in Kazak population.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To explore the association between genetic polymorphisms of glutathione S-transferase (GST) M1 and T1 and susceptibility to Kazak population esophageal cancer (EC). Methods A polymerase chain reaction method was used to detect absence of the GSTM1 and GSTT1 genes in genomic DNA in a high-risk ethnic, Xinjiang, China. Results The frequency of the GSTM1-null genotype in cancer cases (41.47%) was not significantly different from that in controls ( 34.15%). Similarly, no statistically significant differences were observed in the frequency of GSTT1-null genotype in cancer cases (48.78%) compared with control (51.22%). However, the frequency of GSTM1 null alleles genotypes in cases with well-differentiated cancer ( 15.38%) showed a significant decrease compared with that in poor-differentiated cancer ( 53.57%) (P0.05). Conclusions GSTM1-null genotypes may act as risk factor in the development of poor-differentiated esophageal cancer in Kazak population.
Key concepts: Genotype, Esophageal cancer, Glutathione S-transferase, Internal medicine, Allele, Genotype frequency, Biology, Cancer