TY - JOUR
T1 - Adhesivity of colon cancer cells during in vitro metastasis
AU - Tang, Xin
AU - Saif, Taher A.
N1 - Funding Information:
X. T. and T. S. gratefully thank financial support by National Science Foundation Grants No. ECCS 07-25831, 10-02165 and NIH RO1 083272-03. X. T. was funded from NSF Grant 0965918 IGERT: Training the Next Generation of Researchers in Cellular and Molecular Mechanics and BioNanotechnology. X. T. deeply appreciate the generous funding support from Frederic T. and Edith F. Mavis through the Mavis Future Faculty Fellowship (twice, 2010 and 2011). X. T. and T. S. thank the great help from Dr. Yaguang Lian, Dr. Duohai Pan, Mr. Romans Hal, and Mr. Marty Harris at the Micro and Nanotechnology Laboratory (MNTL), Ms. Linna Guan (BioE), Mr. Aaron Silver (MCB) and Ms. Kayla Coleman (MCB), University of Illinois at Urbana-Champaign (UIUC), for bio-MEMS force sensor fabrication, image/data analysis and discussion. X. T. and T. S. gratefully acknowledge Dr. Theresa B. Kuhlenschmidt and Prof. Mark S. Kuhlenschmidt (Vet Med, UIUC) for insightful discussions and great assistance in cell culture and media preparation.
PY - 2013/9
Y1 - 2013/9
N2 - Human colon carcinoma (HCT-8) cells show a stable, metastasis-like phenotype (MLP) when cultured on appropriate soft substrates (21 ∼ 47 kPa). Initially epithelial (E) in nature, the HCT-8 cells become rounded (R) and show a number of metastatic hallmarks after only seven days of culture on soft substrate (Tang et al., [2010] "Mechanical force affects expression of an in vitro metastasis-like phenotype in HCT-8 cells," Biophysical Journal 99, 2460-2469; Tang et al., [2012a] "Attenuation of cell mechanosensitivity in colon cancer cells during in vitro metastasis," PlosONE 7, e50443). Here, we studied the surface nonspecific adhesion of HCT-8 cells throughout the in vitro metastasis process. A novel bio-MEMS force sensor was used to measure the cell-probe nonspecific adhesion. The adhesion characteristics are analyzed using fracture mechanics theory. Our results indicate that the post-metastatic HCT-8 cells (dissociated R cells) display remarkably diminished surface adhesion and are potentially more invasive than original pre-metastatic HCT-8 cells (E cells). To the best of our knowledge, this is the first report of quantitative data showing the changes in cancer cell adhesion and other cellular mechanical properties during the expression of in vitro metastasis-like phenotype.
AB - Human colon carcinoma (HCT-8) cells show a stable, metastasis-like phenotype (MLP) when cultured on appropriate soft substrates (21 ∼ 47 kPa). Initially epithelial (E) in nature, the HCT-8 cells become rounded (R) and show a number of metastatic hallmarks after only seven days of culture on soft substrate (Tang et al., [2010] "Mechanical force affects expression of an in vitro metastasis-like phenotype in HCT-8 cells," Biophysical Journal 99, 2460-2469; Tang et al., [2012a] "Attenuation of cell mechanosensitivity in colon cancer cells during in vitro metastasis," PlosONE 7, e50443). Here, we studied the surface nonspecific adhesion of HCT-8 cells throughout the in vitro metastasis process. A novel bio-MEMS force sensor was used to measure the cell-probe nonspecific adhesion. The adhesion characteristics are analyzed using fracture mechanics theory. Our results indicate that the post-metastatic HCT-8 cells (dissociated R cells) display remarkably diminished surface adhesion and are potentially more invasive than original pre-metastatic HCT-8 cells (E cells). To the best of our knowledge, this is the first report of quantitative data showing the changes in cancer cell adhesion and other cellular mechanical properties during the expression of in vitro metastasis-like phenotype.
KW - Bio-MEMS force actuator/ sensor
KW - Cancer metastasis
KW - Cell adhesion
KW - Cell mechanotransduction
KW - Fracture mechanics
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U2 - 10.1142/S1758825113500257
DO - 10.1142/S1758825113500257
M3 - Article
AN - SCOPUS:84885157092
SN - 1758-8251
VL - 5
JO - International Journal of Applied Mechanics
JF - International Journal of Applied Mechanics
IS - 3
M1 - 1350025
ER -