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DOI 10.1097/00004347-200004000-00008

Медицинская библиотека · International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists · 2000

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

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Hellström A C, Blegen H, Malec M, Silfverswärd C, Lystad S, Børresen-Dale A L, Auer G. Recurrent fallopian tube carcinoma: TP53 mutation and clinical course.. International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists. 2000. DOI: 10.1097/00004347-200004000-00008.

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