The Prevalence of P۵۳ Mutations in Laryngeal Cancer in Kerman
سال انتشار: 1391
نوع سند: مقاله ژورنالی
زبان: فارسی
مشاهده: 44
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شناسه ملی سند علمی:
JR_JKMU-19-6_006
تاریخ نمایه سازی: 14 اسفند 1402
چکیده مقاله:
Background &Aims: Laryngeal cancer is the second common cancer of respiratory tract, following the lung cancer. Carcinogenesis is a complex multistage process; molecular genetics has provided the evidence that activation of proto-oncogene and loss or inactivation of tumor suppressor genes (TSG) are involved in a large number of malignancies. One of the earliest significant tumor suppressor genes identified in head and neck squamous cell carcinoma (HNSCC) was P۵۳ have a role in growth suppression activities. Thus, when P۵۳ is deleted or silenced, the cell develops a selective growth advantage and becomes a cancer. Mutations in P۵۳ are correlated with poorer survival and response to treatment. The aim of this study was to survey the prevalence of P۵۳ gene mutation in patients with laryngeal cancer and to select an appropriate method of treatment. Methods: The samples were ۵۲ patients with laryngeal cancer diagnosis have been treated by surgery. Investigation of TP۵۳ mutation where performed by multiple ligation probe amplification (MLPA) technique which analyze the full length of gene from exon ۱ to ۱۲. Results: The TP۵۳ mutation was discovered in ۸۰.۸ percent of samples. By contrast between two main forms of mutation (i.e. deletions and duplications), we found that the deletions mostly occurred within exons ۱, ۳, ۶, ۹ and ۱۲ by ۵۹.۶ percent and duplications observed in exons ۱, ۲, ۷, ۸ and ۱۱ by ۲۱.۲ percent. Conclusion: Considering our results and reminding this fact that nowadays the definitive diagnosis of laryngeal cancer is made using biopsy and pathology techniques, we suggest that all biopsy specimens should be tested and those confirmed positive for TP۵۳ mutations need some further decisions by physicians.
نویسندگان
M.A Damghani
Assistant Professor of Ear, Nose and Throat, Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
M.R Bazrafshani
Assistant Professor of Medical Genetics, Physiology Research Center & Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
TR Mirshekari
Clinical Pathologist, Shafa Hospital, Kerman University of Medical Sciences, Kerman, Iran