<i>TP53</i> mutations and breast cancer prognosis: Particularly poor survival rates for cases with mutations in the zinc‐binding domains

Anne‐Lise Børresen(Norwegian Cancer Society), Tone Ikdahl Andersen(Norwegian Cancer Society), Jórunn E. Eyfjörd(Icelandic Cancer Society), Renée S. Cornelis(Leiden University), Steinunn Thorlacius(Icelandic Cancer Society), Åke Borg(Lund University), Ulla Johansson(Lund University), Charles Theillet(Institut de Génétique Moléculaire de Montpellier), Siegfried Scherneck(Max Delbrück Center), Susanne Hartman(Max Delbrück Center), Cees J. Cornelisse(Leiden University), Eivind Hovig(Norwegian Cancer Society), Peter Devilee(Leiden University)
Genes Chromosomes and Cancer
September 1, 1995
Cited by 181

Abstract

Acquired mutations in TP53 as well as immunohistochemically detectable protein expression have been implicated as prognostic factors for breast cancer. We have evaluated the relationship between mutations detected in 119 breast tumours and various clinicohistopathological indices, stratifying the mutations according to the functional domains as defined by the recent elucidation of the crystal structure of the protein. Patients with missense mutations located in regions encoding parts of the protein involved in zinc-binding had significantly decreased disease-free and overall survival relative to patients whose tumours had mutations in other domains. These results indicate that these biochemically defined domains also have biological relevance in terms of breast cancer disease course, and suggest that some mutations in TP53, more than others, can contribute to the development of clinically more aggressive and perhaps treatment resistant breast tumours. When confirmed, this will be of potential importance in predicting the clinical behaviour of breast cancer and its responsiveness to therapy.


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