In vivo capture and label-free detection of early metastatic cells

被引:121
作者
Azarin, Samira M. [1 ]
Yi, Ji [2 ]
Gower, M. [3 ]
Aguado, Brian A. [2 ]
Sullivan, Megan E. [4 ]
Goodman, Ashley G. [5 ]
Jiang, Eric J. [5 ]
Rao, Shreyas S. [5 ]
Ren, Yinying [5 ]
Tucker, Susan L. [6 ]
Backman, Vadim [2 ,7 ,8 ]
Jeruss, Jacqueline S. [9 ,10 ]
Shea, Lonnie D. [11 ,12 ,13 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
[3] Univ S Carolina, Dept Chem Engn, Columbia, SC 29208 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Pathol, Evanston, IL 60611 USA
[5] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[6] Univ Texas Houston, MD Anderson Canc Ctr, Dept Bioinformat & Computat Biol, Houston, TX 77030 USA
[7] Northwestern Univ, Chem Life Proc Inst CLP, Evanston, IL 60208 USA
[8] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[9] Univ Michigan, Dept Surg, Ann Arbor, MI 48105 USA
[10] Northwestern Univ, Dept Obstet & Gynecol, Chicago, IL 60611 USA
[11] Northwestern Univ, Inst BioNano Technol Med IBNAM, Chicago, IL 60611 USA
[12] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48105 USA
[13] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48105 USA
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
基金
美国国家卫生研究院;
关键词
CIRCULATING TUMOR-CELLS; OPTICAL COHERENCE TOMOGRAPHY; TISSUE-ENGINEERING SCAFFOLDS; CONTINUOUS RANDOM-MEDIA; BREAST-CANCER CELLS; SUPPRESSOR-CELLS; PREMETASTATIC NICHE; BORN APPROXIMATION; BIOLOGICAL TISSUE; PROGENITOR CELLS;
D O I
10.1038/ncomms9094
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Breast cancer is a leading cause of death for women, with mortality resulting from metastasis. Metastases are often detected once tumour cells affect the function of solid organs, with a high disease burden limiting effective treatment. Here we report a method for the early detection of metastasis using an implanted scaffold to recruit and capture metastatic cells in vivo, which achieves high cell densities and reduces the tumour burden within solid organs 10-fold. Recruitment is associated with infiltration of immune cells, which include Gr1(hi)CD11b(+) cells. We identify metastatic cells in the scaffold through a label-free detection system using inverse spectroscopic optical coherence tomography, which identifies changes to nanoscale tissue architecture associated with the presence of tumour cells. For patients at risk of recurrence, scaffold implantation following completion of primary therapy has the potential to identify metastatic disease at the earliest stage, enabling initiation of therapy while the disease burden is low.
引用
收藏
页数:9
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