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OBJECTIVE To investigate the detection rate of humanpapilloma virus (HPV) DNA in the Kazakh esophageal carcinoma(EC) patients of Xinjiang.METHODS We detected the prevalence of a HPV gene in tumortissues from 318 esophageal squamous cell carcinoma (ESCC).Tumor tissues were kept in formalin and embedded in paraffin.One hundred seventeen samples used crude cell suspension, whilethe other 201 used the method of DNA extraction with phenol-Tris/chloroform. We analyzed the relevance to EC of Kazakh’s inXinjiang.RESULTS In the ESCC samples of Kazakh’s in Xinjiang, totaldetection rate for HPV DNA was 64.5% (205/318). The positiverate of HPV in group of crude cell suspensions was 82.9% (97/117)compared with the rate of 53.7% (108/201) in the group of DNAextraction. The results in the two groups showed significantdiffference (x~2 = 5.711, P < 0.05).CONCLUSION HPV DNA infection may be one of the mostimportant factors related to EC of Kazakh’s in Xinjiang.
OBJECTIVE To investigate the detection rate of human papillomavirus (HPV) DNA in the Kazakh esophageal carcinoma (EC) patients of Xinjiang. METHODS We detected the prevalence of a HPV gene in tumortissues from 318 esophageal squamous cell carcinoma (ESCC) .Tumor tissues were kept in formalin and embedded in paraffin. One hundred seventeen samples used crude cell suspension, while the other 201 used the method of DNA extraction with phenol-Tris / chloroform. Xinjiang, totaldetection rate for HPV DNA was 64.5% (205/318). The positive rate of HPV in group of crude cell suspensions was 82.9% (97/117) compared with the rate of 53.7% (108/201) in the group of DNA results showed that the two groups showed significant differerence (x ~ 2 = 5.711, P <0.05) .CONCLUSION HPV DNA infection may be one of the mostimportant factors related to EC of Kazakh’s in Xinjiang.