Objective: To investigate the status of p16 gene in nasopharyngeal carcinoma (NPC). Methods: Total of 48 NPC cases and correspondent tumor-adjacent were detected for p16 gene munations by using multiplex polymerase chain reaction (PCR) and single strand conformation polymorphism (SSCP) respectively. Results: Among 48 NPC cases, 16 cases homozygous deletions and mutation were not identified. However, deletion and mutation were not found in all the tumor-adjacent tissues. Conclusions: The data above shows that p16 gene loss in high frequency in nasopharyngeal carcinoma. The alteration of p16 gene may play an important role in nasopharyngeal carcinoma.