In vivo MRI of cancer cell fate at the single-cell level in a mouse model of breast cancer metastasis to the brain

被引:233
作者
Heyn, Chris
Ronald, John A.
Ramadan, Soha S.
Snir, Jonatan A.
Barry, Andrea M.
MacKenzie, Lisa T.
Mikulis, David J.
Palmieri, Diane
Bronder, Julie L.
Steeg, Patricia S.
Yoneda, Toshiyuki
MacDonald, Ian C.
Chambers, Ann F.
Rutt, Brian K.
Foster, Paula J.
机构
[1] Robarts Res Inst, Imaging Res Labs, London, ON N6A 5K8, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[3] Univ Western Ontario, Dept Med Biophys, London, ON, Canada
[4] London Reg Canc Program, London, ON, Canada
[5] Univ Hlth Network, Toronto Western Hosp, Dept Med Imaging, Toronto, ON, Canada
[6] NCI, Womens Canc Sect, Mol Pharmacol Lab, Ctr Canc Res, Bethesda, MD USA
[7] Univ Texas, Hlth Sci Ctr, San Antonio, TX 78285 USA
关键词
cellular MRI; iron oxide; metastasis; cancer; cell tracking;
D O I
10.1002/mrm.21029
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Metastasis (the spread of cancer from a primary tumor to secondary organs) is responsible for most cancer deaths. The ability to follow the fate of a population of tumor cells over time in an experimental animal would provide a powerful new way to monitor the metastatic process. Here we describe a magnetic resonance imaging (MRI) technique that permits the tracking of breast cancer cells in a mouse model of brain metastasis at the single-cell level. Cancer cells that were injected into the left ventricle of the mouse heart and then delivered to the brain were detectable on MR images. This allowed the visualization of the initial delivery and distribution of cells, as well as the growth of tumors from a subset of these cells within the whole intact brain volume. The ability to follow the metastatic process from the single-cell stage through metastatic growth, and to quantify and monitor the presence of solitary undivided cells will facilitate progress in understanding the mechanisms of brain metastasis and tumor dormancy, and the development of therapeutics to treat this disease.
引用
收藏
页码:1001 / 1010
页数:10
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