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231223s2010 xx |||||o 00| ||eng c |
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|a 10.1021/la904678p
|2 doi
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|a pubmed24n0650.xml
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|a (DE-627)NLM195099192
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|a (NLM)20155985
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|a DE-627
|b ger
|c DE-627
|e rakwb
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| 041 |
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|a eng
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| 100 |
1 |
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|a Myung, Ja Hye
|e verfasserin
|4 aut
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| 245 |
1 |
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|a Enhanced tumor cell isolation by a biomimetic combination of E-selectin and anti-EpCAM
|b implications for the effective separation of circulating tumor cells (CTCs)
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| 264 |
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|c 2010
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| 336 |
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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| 500 |
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|a Date Completed 08.09.2010
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|a Date Revised 20.10.2021
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|a published: Print
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|a Citation Status MEDLINE
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|a The selective detection of circulating tumor cells (CTCs) is of significant clinical importance for the clinical diagnosis and prognosis of cancer metastasis. However, largely because of the extremely low number of CTCs (as low as 1 in 10(9) hematologic cells) in the blood of patients, effective detection and separation of the rare cells remain a tremendous challenge. Cell rolling is known to play a key role in physiological processes such as the recruitment of leukocytes to sites of inflammation and selectin-mediated CTC metastasis. Furthermore, because CTCs typically express the epithelial-cell adhesion molecule (EpCAM) on the surface whereas normal hematologic cells do not, substrates with immobilized antibody against EpCAM may specifically interact with CTCs. In this article, we created biomimetic surfaces functionalized with P- and E-selectin and anti-EpCAM that induce different responses in HL-60 (used as a model of leukocytes in this study) and MCF-7 (a model of CTCs) cells. HL-60 and MCF-7 cells showed different degrees of interaction with P-/E-selectin and anti-EpCAM at a shear stress of 0.32 dyn/cm(2). HL-60 cells exhibited rolling on P-selectin-immobilized substrates at a velocity of 2.26 +/- 0.28 microm/s whereas MCF-7 cells had no interaction with the surface. Both cell lines, however, had interactions with E-selectin, and the rolling velocity of MCF-7 cells (4.24 +/- 0.31 microm/s) was faster than that of HL-60 cells (2.12 +/- 0.15 microm/s). However, only MCF-7 cells interacted with anti-EpCAM-coated surfaces, forming stationary binding under flow. More importantly, the combination of the rolling (E-selectin) and stationary binding (anti-EpCAM) resulted in substantially enhanced separation capacity and capture efficiency (more than 3-fold enhancement), as compared to a surface functionalized solely with anti-EpCAM that has been commonly used for CTC capture. Our results indicate that cell-specific detection and separation may be achieved through mimicking the biological processes of combined dynamic cell rolling and stationary binding, which will likely lead to a CTC detection device with significantly enhanced specificity and sensitivity without a complex fabrication process
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|a Journal Article
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|a Research Support, N.I.H., Extramural
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| 650 |
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|a Research Support, U.S. Gov't, Non-P.H.S.
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| 650 |
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7 |
|a Antigens, Neoplasm
|2 NLM
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| 650 |
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7 |
|a Cell Adhesion Molecules
|2 NLM
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| 650 |
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|a E-Selectin
|2 NLM
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| 650 |
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7 |
|a Epithelial Cell Adhesion Molecule
|2 NLM
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| 700 |
1 |
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|a Launiere, Cari A
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Eddington, David T
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Hong, Seungpyo
|e verfasserin
|4 aut
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| 773 |
0 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 26(2010), 11 vom: 01. Juni, Seite 8589-96
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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| 773 |
1 |
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|g volume:26
|g year:2010
|g number:11
|g day:01
|g month:06
|g pages:8589-96
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| 856 |
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|u http://dx.doi.org/10.1021/la904678p
|3 Volltext
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|d 26
|j 2010
|e 11
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|h 8589-96
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