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TP53 and MYC gene alterations independently predict poor prognosis in breast cancer patients
Author(s) -
Berns Els M.J. J.,
Klijn Jan G. M.,
Smid Marcel,
van Staveren Iris L.,
Look Maxime P.,
van Putten Wim L. J.,
Foekens John A.
Publication year - 1996
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/(sici)1098-2264(199607)16:3<170::aid-gcc3>3.0.co;2-w
Subject(s) - breast cancer , exon , oncogene , medicine , univariate analysis , biology , oncology , single strand conformation polymorphism , proportional hazards model , lymph node , progesterone receptor , cancer research , hormone receptor , estrogen receptor , cancer , gene , multivariate analysis , genetics , cell cycle
We intended to establish the frequency of exon‐specific TP53 gene alterations and the relation to patient and tumor characteristics and clinical outcome of patients with breast cancer. By using polymerase chain reaction‐single‐strand conformation polymorphism analysis (PCR‐SSCP) and sequencing techniques, TP53 gene alterations were found in 59 (32%) of the 187 samples studied. Most of the TP53 changes (37%) were observed in exon 7. In patients with known follow up (median, 107 months), there was no significant association of the frequency of TP53 mutation with menopausal or nodal status, tumor size, or progesterone receptor status. TP53 gene alterations were more frequently present in estrogen receptor (ER)‐negative (ER − ) tumors ( P = 0.04) and in tumors with an amplified HER2/NEU oncogene ( P = 0.03). Univariate analysis showed that patients with a mutated TP53 in their primary tumors had shorter relapse‐free ( P = 0.01) and overall ( P = 0.03) survival. Patients with a TP53 gene mutation in exon 8 may be identified as having a particularly rapid rate of relapse. In Cox multivariate regression analysis, which included age, menopausal status, lymph node status, tumor size, steroid‐hormone‐receptor status, and oncogene amplifications, both TP53 gene alteration and MYC amplification independently predicted poor prognosis, with relative hazard rates for TP53 and MYC of 1.8 and 1.6, respectively, in analysis for relapse‐free survival and of 1.7 and 1.6, respectively, in analysis for overall survival. Genes Chromosom Cancer 16:170–179 (1996). © 1996 Wiley‐Liss, Inc.