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Recurrent fallopian tube carcinoma: TP53 mutation and clinical course.
Hellström, A C; Blegen, H; Malec, M; Silfverswärd, C; Lystad, S; Børresen-Dale, A L; Auer, G.
Afiliación
  • Hellström AC; Department of Gynaecological Oncology, Karolinska Hospital and Institutet, Stockholm, Sweden.
Int J Gynecol Pathol ; 19(2): 145-51, 2000 Apr.
Article en En | MEDLINE | ID: mdl-10782411
ABSTRACT
Primary fallopian tube carcinoma is a rare, aggressive gynecological cancer; little is known about its cause. Previous studies have indicated that p53 immunopositivity is correlated with short-term survival in primary fallopian tube carcinoma. We examined p53 and p21/WAF1 immunostaining and TP53 mutation in exons 5 to 8 by single-stranded conformation polymorphism and constant denaturant gel electrophoresis in nine cases of primary fallopian tube carcinoma and their metastases/recurrences from patients who survived for between a few months and more than 20 years after diagnosis. We found that 1.) p53 immunopositivity without detectable p21/WAF1 immunostaining did not correlate with TP53 mutations in the conserved domains; 2.) mutations in TP53 occurred in two metastases/recurrences but not in their corresponding primary tumors; 3.) in two cancers, a TP53 mutation was observed in the primary tumor but not in the metastases/recurrences; 4.) constant denaturant gel electrophoresis seems to be more sensitive than single-stranded conformation polymorphism in detecting TP53 mutations; and 5.) in the nine cases studied, p53 immunoreactivity and/or TP53 mutation analysis did not correlate with tumor progression, survival, or response to treatment.
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Base de datos: MEDLINE Asunto principal: Genes p53 / Neoplasias de las Trompas Uterinas / Mutación / Recurrencia Local de Neoplasia Idioma: En Revista: Int J Gynecol Pathol Año: 2000 Tipo del documento: Article
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Base de datos: MEDLINE Asunto principal: Genes p53 / Neoplasias de las Trompas Uterinas / Mutación / Recurrencia Local de Neoplasia Idioma: En Revista: Int J Gynecol Pathol Año: 2000 Tipo del documento: Article