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Occurrence and expression of p53 suppressor gene and c‐Myc oncogene in dog eyelid tumors
Authors:Rodrigo Antonio Lopes  Tereza Cristina Cardoso  Maria Cecília Rui Luvizotto  Alexandre Lima De Andrade
Institution:1. Postgraduate Programme in Animal Science, Faculty of Odontology, Veterinary Science Course, Unesp, State of S?o Paulo University, Ara?atuba‐SP, Brazil;2. Department of Support, Production and Animal Science, Faculty of Odontology, Veterinary Science Course, Unesp, State of S?o Paulo University, Ara?atuba‐SP, Brazil;3. Department of Animal Clinics, Surgery and Reproduction, Faculty of Odontology, Veterinary Science Course, Unesp, State of S?o Paulo University, Ara?atuba‐SP, Brazil
Abstract:Purpose To detect the occurrence and expression of the suppressor gene p53 and of the oncogene c‐Myc in eyelid tumors of dogs using the PCR, RT‐PCR, PCR‐ELISA and RT‐PCR‐ELISA techniques. These genes have not been described in dog eyelid tumors before. Methods Nine samples of eyelid or third eyelid epithelial tumors were obtained from the archives of the Department of Veterinary Pathology. Tumor diagnosis was confirmed by evaluation of hematoxylin‐eosin stained sections, and immunohistochemistry for cytokeratin AE1/AE3 and vimentin V9. A canine mammary tumor was used for positive control. Agarose gel electrophoresis, PCR‐ELISA and RT‐PCR‐ELISA were used to detect p53 and c‐Myc genes. Results The occurrence of p53 was detected in most of the eyelid tumors and third eyelid tumors studied (88.8%, n = 8) and was expressed in 75% of the positive samples, as indicated by ELISA. The c‐Myc gene was found in 77.7% (n = 7) of the samples and was expressed in eight samples. Conclusions Eyelid and third eyelid tumors of dogs express both the p53 and the c‐Myc genes as shown by PCR and RT‐PCR. However, PCR ELISA and RT‐PCR ELISA were more efficient in assessing occurrence and expression of these genes because they identified amplified products that were not detected by agarose gel electrophoresis.
Keywords:c‐Myc  dog  ELISA  eyelid tumors  p53  PCR
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