Microfluidics separation reveals the stem-cell-like deformability of tumor-initiating cells

被引:165
|
作者
Zhang, Weijia [2 ,3 ,4 ]
Kai, Kazuharu [1 ]
Choi, Dong Soon [3 ]
Iwamoto, Takayuki [1 ]
Nguyen, Yen H. [2 ,3 ,4 ]
Wong, Helen [3 ]
Landis, Melissa D. [3 ]
Ueno, Naoto T. [1 ]
Chang, Jenny [3 ]
Qin, Lidong [2 ,3 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Morgan Welch Inflammatory Breast Canc Res Program, Breast Canc Translat Res Lab, Houston, TX 77030 USA
[2] Methodist Hosp, Res Inst, Dept Nanomed, Houston, TX 77030 USA
[3] Methodist Hosp, Res Inst, Methodist Canc Ctr, Houston, TX 77030 USA
[4] Cornell Univ, Weill Med Coll, Dept Cell & Dev Biol, New York, NY 10065 USA
关键词
cell mechanics; cytoskeleton; genomic profiling; CANCER-CELL; MECHANICS; CYTOSKELETON; METASTASIS; PROTEINS; THERAPY; NUCLEUS; NETWORK; FUTURE;
D O I
10.1073/pnas.1209893109
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
Here we report a microfluidics method to enrich physically deformable cells by mechanical manipulation through artificial microbarriers. Driven by hydrodynamic forces, flexible cells or cells with high metastatic propensity change shape to pass through the microbarriers and exit the separation device, whereas stiff cells remain trapped. We demonstrate the separation of (i) a mixture of two breast cancer cell types (MDA-MB-436 and MCF-7) with distinct deformabilities and metastatic potentials, and (ii) a heterogeneous breast cancer cell line (SUM149), into enriched flexible and stiff subpopulations. We show that the flexible phenotype is associated with overexpression of multiple genes involved in cancer cell motility and metastasis, and greater mammosphere formation efficiency. Our observations support the relationship between tumor-initiating capacity and cell deformability, and demonstrate that tumor-initiating cells are less differentiated in terms of cell biomechanics.
引用
收藏
页码:18707 / 18712
页数:6
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