P53 IMMUNOREACTIVITY IN HUMAN-MALIGNANT MELANOMA AND DYSPLASTIC NEVI
P53 IMMUNOREACTIVITY IN HUMAN-MALIGNANT MELANOMA AND DYSPLASTIC NEVI
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DOI:
10.1111/j.1365-2133.1993.tb00253.x
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发表时间:
1993-06-01
影响因子:
10.3
通讯作者:
MACDONALD, DM
中科院分区:
文献类型:
--
作者:
MCGREGOR, JM;YU, CCW;MACDONALD, DM
Expression of the tumour suppressor protein, p53, was determined in 77 cutaneous melanocytic lesions, and in five lymph node metastases from malignant melanoma, in an immunohistochemical study employing CM-1, an antiserum raised against recombinant human p53 protein. Because wild-type p53 protein is rapidly degraded in normal cells, p 5 3 immunoreactivity suggests the presence of an abnormally stable p 5 3 protein. This may occur through either post-translational mechanisms or gene mutation.A highly significant correlation was found between p53 immunoreactivity and malignancy in melanocytic lesions (P < 0.0001). Overall, p53 immunoreactivity was observed in 63% of tumour specimens examined, but not in benign melanocytic naevi, although occasional foci of weak nuclear p53 immunoreactivity were observed in a minority of dysplastic naevi and a solitary Spitz naevus. A significant correlation was also found between strong p53 immunoreactivity and malignant melanomas associated with a poor prognosis (P = 0.008).These data suggest an important role for p 5 3 tumour suppressor protein in the biology of human cutaneous malignant melanoma.