Emerging drugs for targeted therapy of bladder cancer

被引:9
作者
Agarwal, Piyush K.
Black, Peter C.
McConkey, David J.
Dinney, Colin P. N.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Urol, Unit 1373, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Canc Biol, Unit 1373, Houston, TX 77030 USA
关键词
bladder cancer; epidermal growth factor receptor (EGFR); growth factor targeted therapy; vascular endothelial growth factor receptor (VEGFR);
D O I
10.1517/14728214.12.3.435
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Although chemotherapy has improved the treatment of metastatic bladder cancer, resection and continual surveillance remain the modalities used for treatment of organ-confined disease. More targeted therapies are needed to address the shortcomings of existing treatments. The authors recently became aware of the overexpression of tyrosine kinase growth factor receptors in a variety of malignancies. These receptor tyrosine kinases are coupled to several proliferative and antiapoptotic pathways that drive cancer cell growth. Targeted small-molecule therapies, including monoclonal antibodies and tyrosine kinase inhibitors, directed at these receptors have proven effective against a variety of tumor models. in this report, the authors summarize the results of several such studies and discuss the rationale and potential use of novel targeted drugs in the treatment of bladder cancer.
引用
收藏
页码:435 / 448
页数:14
相关论文
共 94 条
[1]
Neoadjuvant chemotherapy in invasive bladder cancer:: Update of a systematic review and meta-analysis of individual patient data [J].
Abol-Enein, H ;
Bassi, P ;
Boyer, M ;
Coppin, CML ;
Cortesi, E ;
Grossman, HB ;
Hall, RR ;
Horwich, A ;
Malmström, PU ;
Martinez-Piñeiro, JA ;
Sengelov, L ;
Sherif, A ;
Wallace, DMA ;
Bono, AV ;
Goebell, PJ ;
Groshen, S ;
Torti, FM ;
Clarke, NW ;
Roberts, JT ;
Sylvester, R ;
Parmar, MKB ;
Stewart, LA ;
Tierney, JF ;
Vale, CL .
EUROPEAN UROLOGY, 2005, 48 (02) :202-206
[2]
Protein kinases as drug targets in cancer [J].
Arslan, Mehmet Alper ;
Kutuk, Ozgur ;
Basaga, Huveyda .
CURRENT CANCER DRUG TARGETS, 2006, 6 (07) :623-634
[3]
Phase I studies of anti-epidermal growth factor receptor chimeric antibody C225 alone and in combination with cisplatin [J].
Baselga, J ;
Pfister, D ;
Cooper, MR ;
Cohen, R ;
Burtness, B ;
Bos, M ;
D'Andrea, G ;
Seidman, A ;
Norton, L ;
Gunnett, K ;
Falcey, J ;
Anderson, V ;
Waksal, H ;
Mendelsohn, J .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (04) :904-914
[4]
Critical update and emerging trends in epidermal growth factor receptor targeting in cancer [J].
Baselga, J ;
Arteaga, CL .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2445-2459
[5]
Baselga J, 2001, EUR J CANCER, V37, pS16
[6]
Targeting tyrosine kinases in cancer: The second wave [J].
Baselga, Jose .
SCIENCE, 2006, 312 (5777) :1175-1178
[7]
BATRA SK, 1995, CELL GROWTH DIFFER, V6, P1251
[8]
Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors [J].
Bianco, R ;
Shin, I ;
Ritter, CA ;
Yakes, FM ;
Basso, A ;
Rosen, N ;
Tsurutani, J ;
Dennis, PA ;
Mills, GB ;
Arteaga, CL .
ONCOGENE, 2003, 22 (18) :2812-2822
[9]
Frequent FGFR3 mutations in papillary non-invasive bladder (pTa) tumors [J].
Billerey, C ;
Chopin, D ;
Aubriot-Lorton, MH ;
Ricol, D ;
de Medina, SGD ;
Van Rhijn, B ;
Bralet, MP ;
Lefrere-Belda, MA ;
Lahaye, JB ;
Abbou, CC ;
Bonaventure, J ;
Zafrani, ES ;
van der Kwast, T ;
Thiery, JP ;
Radvanyi, F .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (06) :1955-1959
[10]
Mutations within the kinase domain and truncations of the epidermal growth factor receptor are rare events in bladder cancer: Implications for therapy [J].
Blehm, Kelly N. ;
Spiess, Philippe E. ;
Bondaruk, Jolanta E. ;
Dujka, Melanie E. ;
Villares, Gabriel J. ;
Zhao, Yi-jue ;
Bogler, Oliver ;
Aldape, Kenneth D. ;
Grossman, H. Barton ;
Adam, Liana ;
McConkey, David J. ;
Czerniak, Bogdan A. ;
Dinney, Colin P. ;
Bar-Eli, Menashe .
CLINICAL CANCER RESEARCH, 2006, 12 (15) :4671-4677