Selective measurement and manipulation of adhesion forces between cancer cells and bone marrow endothelial cells using atomic force microscopy

Nanomedicine

Volumn 8, Issue 6, 2013, Pages 921-934

  Reeves, Kimberley J ^a   Hou, Jia ^a   Higham, Susan E ^a   Sun, Zhe ^b   Trzeciakowski, Jerome P ^c   Meininger, Gerald A ^b   Brown, Nicola J ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b UNIVERSITY OF MISSOURI   (United States)

^c TEXAS A AND M UNIVERSITY   (United States)

Author keywords

adhesion molecule; atomic force microscopy; bone marrow endothelial cell; cell elasticity; cell cell adhesion; force spectroscopy; metastasis; prostate cancer

Indexed keywords

BETA1 INTEGRIN; BLOCKING ANTIBODY; CONCANAVALIN A; INTERCELLULAR ADHESION MOLECULE 1; PADGEM PROTEIN; VASCULAR CELL ADHESION MOLECULE 1; ZOLEDRONIC ACID;

ARTICLE; ATOMIC FORCE MICROSCOPY; BONE MARROW CELL; CANCER CELL; CELL ADHESION; CELL INTERACTION; CELL MIGRATION; CELL STRUCTURE; CONTROLLED STUDY; ELASTICITY; ENDOTHELIUM CELL; FORCE; HUMAN; HUMAN CELL; IN VITRO STUDY; MALE; PRIORITY JOURNAL; PROSTATE CANCER; RIGIDITY; SPECTROSCOPY; WESTERN BLOTTING;

EID: 84878732363     PISSN: 17435889     EISSN: 17486963     Source Type: Journal    
DOI: 10.2217/nnm.12.139     Document Type: Article

References (35)

1. Jemal A, Siegel R, Ward E, Murray T, Xu J, Thun MJ. Cancer statistics, 2007. CA Cancer J. Clin. 57(1), 43-66 (2007).
2. Lange PH, Vessella RL. Mechanisms, hypotheses and questions regarding prostate cancer micrometastases to bone. Cancer Metastasis Rev. 17(4), 331-336 (1998).
3. Mason MD, Davies G, Jiang WG. Cell adhesion molecules and adhesion abnormalities in prostate cancer. Crit. Rev. Oncol. Hematol. 41(1), 11-28 (2002).
4. Honn KV, Tang DG. Adhesion molecules and tumor cell interaction with endothelium and subendothelial matrix. Cancer Metastasis Rev. 11(3-4), 353-375 (1992).
5. Scott LJ, Clarke NW, George NJ, Shanks JH, Testa NG, Lang SH. Interactions of human prostatic epithelial cells with bone marrow endothelium: binding and invasion. Br. J. Cancer 84(10), 1417-1423 (2001).
6. Soligo D, Schiro R, Luksch R et al. Expression of integrins in human bone marrow. Br. J. Haematol. 76(3), 323-332 (1990).
7. Nagle RB, Knox JD, Wolf C, Bowden GT, Cress AE. Adhesion molecules, extracellular matrix, and proteases in prostate carcinoma. J. Cell. Biochem. 19, 232-237 (1994).
8. Rokhlin OW, Cohen MB. Expression of cellular adhesion molecules on human prostate tumor cell lines. Prostate 26(4), 205-212 (1995).
9. Binnig G, Quate CF, Gerber C. Atomic force microscope. Phys. Rev. Lett. 56(9), 930-933 (1986).
10. Butt HJ. Measuring electrostatic, van der Waals, and hydration forces in electrolyte solutions with an atomic force microscope. Biophys. J. 60(6), 1438-1444 (1991).
11. Ducker WA, Senden TJ, Pashley RM. Direct measurements of colloidal forces using an atomic force microscope. Nature 353, 239-241 (1991).
12. Lee GU, Chrisey LA, Colton RJ. Direct measurement of the forces between complementary strands of DNA. Science 266(5186), 771-773 (1994).
13. Moy VT, Florin EL, Gaub HE. Intermolecular forces and energies between ligands and receptors. Science 266(5183), 257-259 (1994).
14. Zhuang X, Rief M. Single-molecule folding. Curr. Opin. Struct. Biol. 13(1), 88-97 (2003).
15. Hansma HG, Kasuya K, Oroudjev E. Atomic force microscopy imaging and pulling of nucleic acids. Curr. Opin. Struct. Biol. 14(3), 380-385 (2004).
16. Zhang X, Wojcikiewicz EP, Moy VT. Dynamic adhesion of T lymphocytes to endothelial cells revealed by atomic force microscopy. Exp. Biol. Med. 231(8), 1306-1312 (2006).
17. Kedrov A, Janovjak H, Sapra KT, Muller DJ. Deciphering molecular interactions of native membrane proteins by single-molecule force spectroscopy. Ann. Rev. Biophys. Biomol. Struct. 36, 233-260 (2007).
18. Cross SE, Jin YS, Rao J, Gimzewski JK. Nanomechanical analysis of cells from cancer patients. Nat. Nanotechnol. 2(12), 780-783 (2007).
19. Sharma S, Santiskulvong C, Bentolila LA, Rao J, Dorigo O, Gimzewski JK. Correlative nanomechanical profiling with superresolution F-actin imaging reveals novel insights into mechanisms of cisplatin resistance in ovarian cancer cells Nanomedicine 8, 757-766 (2012).
20. Ramachandran S, Quist AP, Kumar S, Lal R. Cisplatinnanoliposomes for cancer therapy: AFM and fluorescence imaging of cisplatin encapsulation, stability, cellular uptake, and toxicity. Langmuir 22(19), 8156-8162 (2006).
21. Faria EC, Ma N, Gazi E et al. Measurement of elastic properties of prostate cancer cells using AFM. Analyst 133(11), 1498-1500 (2008).
22. Li QS, Lee GY, Ong CN, Lim CT. AFM indentation study of breast cancer cells. Biochem. Biophys. Res. Commun. 374(4), 609-613 (2008).
23. Docheva D, Padula D, Schieker M, Clausen-Schaumann H. Effect of collagen I and fibronectin on the adhesion, elasticity and cytoskeletal organization of prostate cancer cells. Biochem. Biophys. Res. Commun. 402(2), 361-366 (2010).
24. Puech PH, Taubenberger A, Ulrich F, Krieg M, Muller DJ, Heisenberg CP. Measuring cell adhesion forces of primary gastrulating cells from zebrafish using atomic force microscopy. J. Cell. Sci. 118(Pt 18), 4199-4206 (2005).
25. Green Jr. Bisphosphonates: preclinical review. Oncologist 9(Suppl. 4), 3-13 (2004).
26. Wu X, Sun Z, Foskett A, Trzeciakowski JP, Meininger GA, Muthuchamy M. Cardiomyocyte contractile status is associated with differences in fibronectin and integrin interactions. Am. J. Phys. 298(6), H2071-H2081 (2010).
27. Qiu H, Zhu Y, Sun Z et al. Short communication: vascular smooth muscle cell stiffness as a mechanism for increased aortic stiffness with aging. Circ. Res. 107(5), 615-619 (2010).
28. Sun Z, Martinez-Lemus LA, Hill MA, Meininger GA. Extracellular matrix-specific focal adhesions in vascular smooth muscle produce mechanically active adhesion sites. Am. J. Physiol. Cell Physiol. 295, C268-C278 (2008).
29. Zhu Y, Qiu H, Trzeciakowski JP et al. Temporal analysis of vascular smooth muscle cell elasticity and adhesion reveals oscillation waveforms that differ with aging. Aging Cell doi:10.1111/j.1474-9726.2012.00840.x (2012) (Epub ahead of print).
30. Végh AG, Fazakas C, Nagy K et al. Adhesion and stress relaxation forces between melanoma and cerebral endothelial cells. Eur. Biophys. J. 41(2), 139-145 (2012).
31. Dunford JE, Thompson K, Coxon FP et al. Structure-activity relationships for inhibition of farnesyldiphosphate synthase in vitro and inhibition of bone resorption in vivo by nitrogen-containing bisphosphonates. J. Pharmacol. Exp. Ther. 296(2), 235-242 (2001).
32. Giancotti FG, Tarone G. Positional control of cell fate through joint integrin/receptor protein kinase signaling. Ann. Rev. Cell Dev. Biol. 19, 173-206 (2003).
33. Lo SH. Focal adhesions: what's new inside. Dev. Biol. 294(2), 280-291 (2006).
34. Corso A, Ferretti E, Lunghi M et al. Zoledronic acid down-regulates adhesion molecules of bone marrow stromal cells in multiple myeloma: a possible mechanism for its antitumor effect. Cancer 104(1), 118-125 (2005).
35. Michailidou M, Brown HK, Lefley DV et al. Microvascular endothelial cell responses in vitro and in vivo: modulation by zoledronic acid and paclitaxel? J. Vasc. Res. 47(6), 481-493 (2010).