Cui H, Yang X, He Q
Cancer Institute, CAMS and PUMC, Beijing.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1994 Apr;16(2):109-15.
In this paper, alpha-32P-dCTP-labeled HPV-11 and HPV-16 DNA were used as probe, and slot and Southern blot hybridization techniques were used to detect HPV-11 and HPV-16 DNA related sequences in 37 laryngeal carcinoma tissues taken from patients in Qingdao and Beijing. Using the slot blot technique, 86% (32/37) of the cases showed positive hybridization with HPV-11 probe, while 81% (30/37) showed positive results with HPV-16. Another 81% (30/37) showed positive hybridization with HPV-11 and HPV-16 simultaneously. Using Southern blot hybridization Pst digestion, the hybridization pattern corresponded to that of HPV-16 in 46; (13/28), and none corresponded to HPV-11. The results suggest that HPV-16 may induce laryngeal carcinoma.
本文以α-32P-dCTP标记的HPV-11和HPV-16 DNA为探针,采用斑点杂交和Southern印迹杂交技术,检测青岛和北京两地患者的37份喉癌组织中HPV-11和HPV-16 DNA相关序列。采用斑点杂交技术,86%(32/37)的病例与HPV-11探针杂交呈阳性,而81%(30/37)与HPV-16杂交呈阳性。另有81%(30/37)同时与HPV-11和HPV-16杂交呈阳性。采用Southern印迹杂交Pst消化法,46份(13/28)杂交图谱与HPV-16相符,无一份与HPV-11相符。结果提示HPV-16可能诱发喉癌。