Molecular imaging in prostate cancer

被引:24
作者
Karam, JA
Mason, RP
Koeneman, KS
Antich, PP
Benaim, EA
Hsieh, JT
机构
[1] Univ Texas, SW Med Ctr Dallas, Dept Urol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr Dallas, Dept Radiol, Dallas, TX 75390 USA
关键词
molecular imaging; prostate cancer; PET; MRI; bioluminescence; tumor oximetry; radiolabeled antibodies;
D O I
10.1002/jcb.10636
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
Prostate cancer (PCa) is the most common non-cutaneous malignancy in men. New ways to diagnose this cancer in its early stages are needed. Unique genetic and biochemical changes in the cell pave the way for tumors to grow and metastasize. Novel imaging approaches attempt to detect pathological processes in cancer cells at the molecular level. This has led to the establishment and development of the field of molecular imaging. Positron emission tomography (PET), magnetic resonance spectroscopic imaging (MRSI), magnetic resonance imaging (MRI), and radiolabeled antibodies are a few of the modalities that can detect abnormal tumor metabolic processes in the clinical setting. Other imaging techniques are still in their early phase of development but hold promise for the future, including bioluminescence imaging (BLI), measurement of tumor oxygenation, and measurement of uptake of iodine by tumors. These techniques are non-invasive and can spare the patient undue morbidity, while potentially providing early diagnosis, accurate follow-up and, finally, valuable prognostic information. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:473 / 483
页数:11
相关论文
共 54 条
[1]  
*ACS, 2003, CANC FACTS FIGUR
[2]   Visualization of advanced human prostate cancer lesions in living mice by a targeted gene transfer vector and optical imaging [J].
Adams, JY ;
Johnson, M ;
Sato, M ;
Berger, F ;
Gambhir, SS ;
Carey, M ;
Iruela-Arispe, ML ;
Wu, L .
NATURE MEDICINE, 2002, 8 (08) :891-896
[3]  
Barentsz JO, 1999, J MAGN RESON IMAGING, V10, P295, DOI 10.1002/(SICI)1522-2586(199909)10:3<295::AID-JMRI10>3.0.CO
[4]  
2-Z
[5]  
Bostwick DG, 1998, CANCER-AM CANCER SOC, V82, P2256, DOI 10.1002/(SICI)1097-0142(19980601)82:11<2256::AID-CNCR22>3.0.CO
[6]  
2-S
[7]   Non-destructive quantitation of spermine in human prostate tissue samples using HRMAS 1H NMR spectroscopy at 9.4 T [J].
Cheng, LL ;
Wu, CL ;
Smith, MR ;
Gonzalez, RG .
FEBS LETTERS, 2001, 494 (1-2) :112-116
[8]   Advances in vivo bioluminescence imaging of gene expression [J].
Contag, CH ;
Bachmann, MH .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :235-260
[9]   Cloning and characterization of the thyroid iodide transporter [J].
Dai, G ;
Levy, O ;
Carrasco, N .
NATURE, 1996, 379 (6564) :458-460
[10]  
DeGrado TR, 2001, CANCER RES, V61, P110