Prognostic value of mutations in TP53 and RAS genes in breast cancer

被引:5
作者
Guerra, E
Vacca, G
Palombo, B
Alberti, S [1 ]
机构
[1] Ist Ric Farmacol Mario Negri, Consorzio Mario Negri Sud, Dept Cell Biol & Oncol, Expt Oncol Lab, I-66030 Santa Maria Imbaro, Italy
[2] Univ G Dannunzio, Sch Med, Dept Oncol, Chieti, Italy
关键词
tumor; marker; RAS; TP53; clinical studies;
D O I
10.1177/172460080301800108
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The identification of molecular indicators of higher risk for specific subgroups of cancer patients may allow to develop more aggressive therapeutic strategies aimed at cases with the highest likelihood of response. This would avoid unnecessary toxicity to patients and alleviate the burden of cancer care for healthcare systems. Activated oncogenes and mutated tumor suppressor genes are causal determinants of the appearance and progression of tumors in man. They therefore represent potential indicators of prognosis and/or response to therapy. However, even in cases of well-studied oncogenes and tumor suppressor genes such as TP53 and RAS, their attributed prognostic and predictive value is often based on studies of insufficient statistical power that often lead to conflicting conclusions. Findings in favor or against the use of TP53 and RAS as prognostic and predictive indicators in breast cancer are reviewed and discussed here.
引用
收藏
页码:49 / 53
页数:5
相关论文
共 47 条
[1]   Distinct initiation and maintenance mechanisms cooperate to induce G1 cell cycle arrest in response to DNA damage [J].
Agami, R ;
Bernards, R .
CELL, 2000, 102 (01) :55-66
[2]   Rapid p53 sequence analysis in primary lung cancer using an oligonucleotide probe array [J].
Ahrendt, SA ;
Halachmi, S ;
Chow, JT ;
Wu, L ;
Halachmi, N ;
Yang, SC ;
Wehage, S ;
Jen, J ;
Sidransky, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) :7382-7387
[3]   Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays [J].
Alon, U ;
Barkai, N ;
Notterman, DA ;
Gish, K ;
Ybarra, S ;
Mack, D ;
Levine, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6745-6750
[4]   PROGNOSTIC-SIGNIFICANCE OF TP53 ALTERATIONS IN BREAST-CARCINOMA [J].
ANDERSEN, TI ;
HOLM, R ;
NESLAND, JM ;
HEIMDAL, KR ;
OTTESTAD, L ;
BORRESEN, AL .
BRITISH JOURNAL OF CANCER, 1993, 68 (03) :540-548
[5]  
Berns EMJJ, 2000, CANCER RES, V60, P2155
[6]   Lack of prognostic value of p53 protein expression in node-negative breast cancer [J].
Bianchi, S ;
Calzolari, A ;
Vezzosi, V ;
Zampi, G ;
Cardona, G ;
Cataliotti, L ;
Bonardi, R ;
Ciatto, S .
TUMORI, 1997, 83 (03) :669-672
[7]   STRUCTURE AND EXPRESSION OF ONCOGENES IN SURGICAL SPECIMENS OF HUMAN-BREAST CARCINOMAS [J].
BIUNNO, I ;
POZZI, MR ;
PIEROTTI, MA ;
PILOTTI, S ;
CATTORETTI, G ;
DELLAPORTA, G .
BRITISH JOURNAL OF CANCER, 1988, 57 (05) :464-468
[8]  
Blaszyk H, 2000, INT J CANCER, V89, P32, DOI 10.1002/(SICI)1097-0215(20000120)89:1<32::AID-IJC6>3.0.CO
[9]  
2-G
[10]   TP53 MUTATIONS AND BREAST-CANCER PROGNOSIS - PARTICULARLY POOR SURVIVAL RATES FOR CASES WITH MUTATIONS IN THE ZINC-BINDING DOMAINS [J].
BORRESEN, AL ;
ANDERSEN, TI ;
EYFJORD, JE ;
CORNELIS, RS ;
THORLACIUS, S ;
BORG, A ;
JOHANSSON, U ;
THEILLET, C ;
SCHERNECK, S ;
HARTMAN, S ;
CORNELISSE, CJ ;
HOVIG, E ;
DEVILEE, P .
GENES CHROMOSOMES & CANCER, 1995, 14 (01) :71-75