Diffusion-weighted MRI and response to anti-cancer therapies

被引:10
作者
Galons, JP [1 ]
Morse, DL
Jennings, DR
Gillies, RJ
机构
[1] Univ Arizona, Hlth Sci Ctr, Dept Radiol, Tucson, AZ 85724 USA
[2] Univ Arizona, Hlth Sci Ctr, Dept Mol & Cell Biol, Tucson, AZ 85724 USA
[3] Univ Arizona, Hlth Sci Ctr, Dept Biomed Engn, Tucson, AZ 85724 USA
[4] Univ Arizona, Hlth Sci Ctr, Dept Biochem & Mol Biophys, Tucson, AZ 85724 USA
关键词
D O I
10.1560/GJ5M-PP8R-GHUB-VUUP
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In oncology practice, longitudinal studies are routinely conducted to monitor the size and enhancement of tumors in cancer patients undergoing therapy. Imaging protocols typically use gadolinium-enhanced T-1-weighted images or T-2-weighted images from which tumor size is inferred and tumor response estimated. The past few years have also seen the emergence of diffusion-weighted magnetic resonance imaging (DWMRI) as a potential alternative to monitor therapeutic response (Kauppinen, R.A., NMR Biomed. 2002, 15, 6). The attractiveness of DWMRI resides in its ability to detect local microstructural changes associated with treatment long before their effects are translated into effective size changes. Damage to cell membrane integrity, changes in viscosity, and/or relative size of intra- vs. extracellular compartments all translate into changes in the apparent diffusion coefficient of tumor water measured by DWMRI. This dependence makes DWMRI a particularly sensitive method to detect response to a wide variety of chemotherapeutic agents. This review will focus on the emerging role of DWMRI to monitor the response of tumors to anti-cancer chemotherapies.
引用
收藏
页码:91 / 101
页数:11
相关论文
共 92 条
  • [1] APOPTOSIS - A GENERAL COMMENT
    ALLES, A
    ALLEY, K
    BARRETT, JC
    BUTTYAN, R
    COLUMBANO, A
    COPE, FO
    COPELAN, EA
    DUKE, RC
    FAREL, PB
    GERSHENSON, LE
    GOLDGABER, D
    GREEN, DR
    HONN, KV
    HULLY, J
    ISAACS, JT
    KERR, JFR
    KRAMMER, PH
    LOCKSHIN, RA
    MARTIN, DP
    MCCONKEY, DJ
    MICHAELSON, J
    SCHULTEHERMANN, R
    SERVER, AC
    SZENDE, B
    TOMEI, LD
    TRITTON, TR
    UMANSKY, SR
    VALERIE, K
    WARNER, HR
    [J]. FASEB JOURNAL, 1991, 5 (08) : 2127 - 2128
  • [2] WATER DIFFUSION PERMEABILITY OF HUMAN ERYTHROCYTES STUDIES BY A PULSED GRADIENT NMR TECHNIQUE
    ANDRASKO, J
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 428 (02) : 304 - 311
  • [3] Ballon D, 2000, NMR BIOMED, V13, P321, DOI 10.1002/1099-1492(200010)13:6<321::AID-NBM651>3.0.CO
  • [4] 2-P
  • [5] Characterization of cell volume loss in CEM-C7A cells during dexamethasone-induced apoptosis
    Benson, RSP
    Heer, S
    Dive, C
    Watson, AJM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (04): : C1190 - C1203
  • [6] MECHANISM OF DETECTION OF ACUTE CEREBRAL-ISCHEMIA IN RATS BY DIFFUSION-WEIGHTED MAGNETIC-RESONANCE MICROSCOPY
    BENVENISTE, H
    HEDLUND, LW
    JOHNSON, GA
    [J]. STROKE, 1992, 23 (05) : 746 - 754
  • [7] A multistep model for paclitaxel-induced apoptosis in human breast cancer cell lines
    Blajeski, AL
    Kottke, TJ
    Kaufmann, SH
    [J]. EXPERIMENTAL CELL RESEARCH, 2001, 270 (02) : 277 - 288
  • [8] Quantitative analysis of apoptotic cell death using proton nuclear magnetic resonance spectroscopy
    Blankenberg, FG
    Katsikis, PD
    Storrs, RW
    Beaulieu, C
    Spielman, D
    Chen, JY
    Naumovski, L
    Tait, JF
    [J]. BLOOD, 1997, 89 (10) : 3778 - 3786
  • [9] A necessary role for cell shrinkage in apoptosis
    Bortner, CD
    Cidlowski, JA
    [J]. BIOCHEMICAL PHARMACOLOGY, 1998, 56 (12) : 1549 - 1559
  • [10] Absence of volume regulatory mechanisms contributes to the rapid activation of apoptosis in thymocytes
    Bortner, CD
    Cidlowski, JA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (03): : C950 - C961