Combined modality management of breast cancer: Development of predictive markers through proteomics

被引:14
作者
Chakravarthy, B
Pietenpol, JA
机构
[1] Vanderbilt Univ, Med Ctr, Dept Radiat Oncol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Biochem, Nashville, TN 37232 USA
关键词
D O I
10.1016/S0093-7754(03)00267-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment of localized breast cancer often requires the use of surgery, radiation, and chemotherapy. The optimal sequencing of these treatments remains controversial. Although randomized studies have not found an improvement in survival with the use of neoadjuvant chemotherapy, a higher percentage of patients can undergo breast conservation. This clinical setting also allows us the unique opportunity to measure in vivo response to a select drug or drug combination. While there have been many retrospective studies looking at prognostic markers of response, there have been very few prospective studies developing markers that predict ultimate outcome from a specific drug or drug combination. This review discusses some of the newer technologies being used to develop predictive markers of therapeutic response. Proteomics is the study of the complete set of proteins expressed in a cell. It is a powerful tool to compare two different samples. Serial biopsies that compare the protein profile before and 24 hours after a cycle of chemotherapy may allow us to determine particular protein profiles that predict for ultimate clinical outcome. © 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 36
页数:14
相关论文
共 103 条
[41]   The contribution of molecular markers to the prediction of response in the treatment of breast cancer:: A review of the literature on HER-2, p53and BCL-2 [J].
Hamilton, A ;
Piccart, M .
ANNALS OF ONCOLOGY, 2000, 11 (06) :647-663
[42]   C-erbB-2 in breast cancer: Development of a clinically useful marker [J].
Hayes, DF ;
Thor, AD .
SEMINARS IN ONCOLOGY, 2002, 29 (03) :231-245
[43]  
HENDERSON IC, 1998, P AN M AM SOC CLIN, V17, P101
[44]   10-YEAR RESULTS OF A COMPARISON OF CONSERVATION WITH MASTECTOMY IN THE TREATMENT OF STAGE-I AND STAGE-II BREAST-CANCER [J].
JACOBSON, JA ;
DANFORTH, DN ;
COWAN, KH ;
DANGELO, T ;
STEINBERG, SM ;
PIERCE, L ;
LIPPMAN, ME ;
LICHTER, AS ;
GLATSTEIN, E ;
OKUNIEFF, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (14) :907-911
[45]   AMPLIFICATION OF A NOVEL V-ERBB-RELATED GENE IN A HUMAN MAMMARY-CARCINOMA [J].
KING, CR ;
KRAUS, MH ;
AARONSON, SA .
SCIENCE, 1985, 229 (4717) :974-976
[46]   Clinical course of breast cancer patients with complete pathologic primary tumor and axillary lymph node response to doxorubicin-based neoadjuvant chemotherapy [J].
Kuerer, HM ;
Newman, LA ;
Smith, TL ;
Ames, FC ;
Hunt, KK ;
Dhingra, K ;
Theriault, RL ;
Singh, G ;
Binkley, SM ;
Sneige, N ;
Buchholz, TA ;
Ross, MI ;
McNeese, MD ;
Buzdar, AU ;
Hortobagyi, GN ;
Singletary, SE .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (02) :460-469
[47]   IN-VITRO STUDIES OF TAXOL AS A RADIATION SENSITIZER IN HUMAN TUMOR-CELLS [J].
LIEBMANN, J ;
COOK, JA ;
FISHER, J ;
TEAGUE, D ;
MITCHELL, JB .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (06) :441-446
[48]   Phosphorylation of Bcl-2 is a marker of M phase events and not a determinant of apoptosis [J].
Ling, YH ;
Tornos, C ;
Perez-Soler, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18984-18991
[49]  
Linn SC, 1997, INT J CANCER, V71, P787, DOI 10.1002/(SICI)1097-0215(19970529)71:5<787::AID-IJC16>3.3.CO
[50]  
2-3