Therapeutic Proteins in Tumors and Targeted Therapeutic Agents for Cancer Patients

被引:3
作者
Kesikli, S. Altug [1 ,2 ]
Kilickap, Saadettin [2 ]
机构
[1] Hacettepe Univ, Inst Canc, Dept Basic Oncol, Ankara, Turkey
[2] Hacettepe Univ, Inst Canc, Dept Prevent Oncol, TR-06100 Ankara, Turkey
关键词
Targeted therapy; targeted therapeutic agents; small molecule kinase inhibitors; therapeutic monoclonal antibodies; anti-tumor immune responses; angiogenesis; EGF; VEGF; sorafenib; sunitinib; TYROSINE KINASE INHIBITOR; ANTI-CD20; MONOCLONAL-ANTIBODY; CHRONIC LYMPHOCYTIC-LEUKEMIA; CELL LUNG-CANCER; ACUTE MYELOID-LEUKEMIA; GASTROINTESTINAL STROMAL TUMOR; METASTATIC COLORECTAL-CANCER; DIAGNOSED CHRONIC-PHASE; BREAST-CANCER; GEMTUZUMAB OZOGAMICIN;
D O I
10.2174/092986652012131112123040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The identification of novel molecular targets has paved the way for new treatment options in cancer patients. A number of agents targeting molecules that are crucial both for the tumor and its microenvironment have already been approved by the U. S. Food and Drug Administration for clinical use. The monoclonal antibodies and the small molecule kinase inhibitors constitute two major classes of targeted therapeutic agents, which have apparently different mechanisms of action, toxicity profiles, routes of administration, timing and dosing. Moreover, individual differences in genes regulating the distribution and metabolism of targeted agents evidently influence treatment outcomes. Data regarding the immune-and tumor microenvironment-modulatory properties of most of these agents are either obscure or controversial, as well. Therefore, preclinical animal and human studies that aim to identify the immunological, biological and the pharmacological properties of these novel classes of agents that also employ recent developments in pharmacogenomics and proteomics are warranted.
引用
收藏
页码:1345 / 1359
页数:15
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