Corrigendum to ‘AFM nanoindentation detection of the elastic modulus of tongue squamous carcinoma cells with different metastatic potentials’ [Nanomedicine 9 (2013) 864–874] (S1549963413001573) (10.1016/j.nano.2013.04.001);AFM nanoindentation detection of the elastic modulus of tongue squamous carcinoma cells with different metastatic potentials

Nanomedicine: Nanotechnology, Biology, and Medicine

Volumn 9, Issue 7, 2013, Pages 864-874

  Zhou, Zhoulong ^b   Zheng, Chaoxu ^a   Li, Su ^a   Zhou, Xiaofeng ^c   Liu, Zhonghua ^a   He, Qianting ^a   Zhang, Ningning ^a   Ngan, Alfonso ^b   Tang, Bin ^b,d   Wang, Anxun ^a  

^a SUN YAT SEN UNIVERSITY   (China)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

^c UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^d SOUTHERN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Atomic force microscopy; Elastic modulus; Metastasis; Nanoindentation; Tongue squamous cell carcinoma

Indexed keywords

ATOMIC FORCE MICROSCOPY; CELL CULTURE; ELASTIC MODULI; NANOINDENTATION; PATHOLOGY; PROTEINS;

AFM NANOINDENTATION; CYTOSKELETONS; EPITHELIAL-MESENCHYMAL TRANSITION; METASTASIS; METASTATIC POTENTIAL; MOLECULAR MECHANISM; SQUAMOUS CARCINOMA; SQUAMOUS CELL CARCINOMA;

CELLS;

BETA TUBULIN; F ACTIN; UVOMORULIN; VIMENTIN;

ARTICLE; ATOMIC FORCE MICROSCOPY; CARCINOMA CELL; CELL LINE; CELL NUCLEUS; CELL SIZE; CONTROLLED STUDY; CYTOPLASM; CYTOSKELETON; EPITHELIAL MESENCHYMAL TRANSITION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; METASTASIS POTENTIAL; NANOINDENTATION; NUCLEAR SIZE; PRIMARY CELL CULTURE; SCANNING ELECTRON MICROSCOPY; TONGUE CARCINOMA; WESTERN BLOTTING; WOUND HEALING; YOUNG MODULUS;

ATOMIC FORCE MICROSCOPY; ELASTIC MODULUS; METASTASIS; NANOINDENTATION; TONGUE SQUAMOUS CELL CARCINOMA;

ACTINS; CARCINOMA, SQUAMOUS CELL; CELL LINE, TUMOR; CELL NUCLEUS; CELL NUCLEUS SIZE; CYTOSKELETON; ELASTIC MODULUS; EPITHELIAL-MESENCHYMAL TRANSITION; HUMANS; MICROSCOPY, ATOMIC FORCE; NANOTECHNOLOGY; NEOPLASM METASTASIS; TONGUE NEOPLASMS; TUBULIN; TUMOR MARKERS, BIOLOGICAL;

EID: 84884281372     PISSN: 15499634     EISSN: 15499642     Source Type: Journal    
DOI: 10.1016/j.nano.2017.03.009     Document Type: Erratum

References (49)

1. Ye H., Wang A., Lee B.S., Yu T., Sheng S., Peng T., et al. Proteomic based identification of manganese superoxide dismutase 2 (SOD2) as a metastasis marker for oral squamous cell carcinoma. Cancer Genomics Proteomics 2008, 5:85-94.
2. Liu X., Yu J., Jiang L., Wang A., Shi F., Ye H., et al. MicroRNA-222 regulates cell invasion by targeting matrix metalloproteinase 1 (MMP1) and manganese superoxide dismutase 2 (SOD2) in tongue squamous cell carcinoma cell lines. Cancer Genomics Proteomics 2009, 6:131-139.
3. Jiang L., Dai Y., Liu X., Wang C., Wang A., Chen Z., et al. Identification and experimental validation of G protein alpha inhibiting activity polypeptide 2 (GNAI2) as a microRNA-138 target in tongue squamous cell carcinoma. Hum Genet 2011, 129:189-197.
4. Jiang L., Liu X., Kolokythas A., Yu J., Wang A., Heidbreder C.E., et al. Downregulation of the Rho GTPase signaling pathway is involved in the microRNA-138-mediated inhibition of cell migration and invasion in tongue squamous cell carcinoma. Int J Cancer 2010, 127:505-512.
5. Liu X., Wang C., Chen Z., Jin Y., Wang Y., Kolokythas A., et al. MicroRNA-138 suppresses epithelial-mesenchymal transition in squamous cell carcinoma cell lines. Biochem J 2011, 440:23-31.
6. Liu X., Jiang L., Wang A., Yu J., Shi F., Zhou X. MicroRNA-138 suppresses invasion and promotes apoptosis in head and neck squamous cell carcinoma cell lines. Cancer Lett 2009, 286:217-222.
7. Jin Y., Wang C., Liu X., Mu W., Chen Z., Yu D., et al. Molecular characterization of the microRNA-138-Fos-like antigen 1 (FOSL1) regulatory module in squamous cell carcinoma. J Biol Chem 2011, 286:40104-40109.
8. Wang C., Liu X., Chen Z., Huang H., Jin Y., Kolokythas A., et al. Polycomb group protein EZH2-mediated E-cadherin repression promotes metastasis of oral tongue squamous cell carcinoma. Mol Carcinog 2011, 10.1002/mc.21848.
9. Shoushtari A.N., Szmulewitz R.Z., Rinker-Schaeffer C.W. Metastasis-suppressor genes in clinical practice: lost in translation?. Nat Rev Clin Oncol 2011, 8:333-342.
10. Suresh S. Biomechanics and biophysics of cancer cells. Acta Biomater 2007, 3:413-438.
11. Swaminathan V., Mythreye K., O'Brien E.T., Berchuck A., Blobe G.C., Superfine R. Mechanical stiffness grades metastatic potential in patient tumor cells and in cancer cell lines. Cancer Res 2011, 71:5075-5080.
12. Cross S.E., Jin Y.S., Tondre J., Wong R., Rao J., Gimzewski J.K. AFM-based analysis of human metastatic cancer cells. Nanotechnology 2008, 19:384003.
13. Suresh S. Nanomedicine: elastic clues in cancer detection. Nat Nanotechnol 2007, 2:748-749.
14. Lekka M., Laidler P. Applicability of AFM in cancer detection. Nat Nanotechnol 2009, 4:72.
15. Chen K., Li D., Jiang Y.H., Yao W.J., Wang X.J., Wei X.C., et al. Influence of expressed TRAIL on biophysical properties of the human leukemic cell line Jurkat. Cell Res 2004, 14:161-168.
16. Song J.W., Cavnar S.P., Walker A.C., Luker K.E., Gupta M., Tung Y.C., et al. Microfluidic endothelium for studying the intravascular adhesion of metastatic breast cancer cells. PLoS One 2009, 4:e5756.
17. Ngan A.H.W., Tang B. Viscoelastic effects during unloading in depth-sensing indentation. Journal of Materials Research 2002, 17:2604-2610.
18. Tang B., Ngan A.H.W. A rate-jump method for characterization of soft tissues using nanoindentation techniques. Soft Matter 2012, 8:5974-5979.
19. Zhou Z.L., Ngan A.H.W., Tang B., Wang A.X. Reliable measurement of elastic modulus of cells by nanoindentation in an atomic force microscope. J Mech Behav Biomed Mater 2012, 8:134-142.
20. Tang B., Ngan A.H.W. Nanoindentation using an atomic force microscope. Philosophical Magazine 2011, 91:1329-1338.
21. Guck J., Schinkinger S., Lincoln B., Wottawah F., Ebert S., Romeyke M., et al. Optical deformability as an inherent cell marker for testing malignant transformation and metastatic competence. Biophys J 2005, 88:3689-3698.
22. Remmerbach T.W., Wottawah F., Dietrich J., Lincoln B., Wittekind C., Guck J. Oral cancer diagnosis by mechanical phenotyping. Cancer Res 2009, 69:1728-1732.
23. Buckley S.T., Davies A.M., Ehrhardt C. Atomic force microscopy and high-content analysis: two innovative technologies for dissecting the relationship between epithelial-mesenchymal transition-related morphological and structural alterations and cell mechanical properties. Methods Mol Biol 2011, 784:197-208.
24. Rolli C.G., Seufferlein T., Kemkemer R., Spatz J.P. Impact of tumor cell cytoskeleton organization on invasiveness and migration: a microchannel-based approach. PLoS One 2010, 5:e8726.
25. Gerlitz G., Bustin M. The role of chromatin structure in cell migration. Trends Cell Biol 2011, 21:6-11.
26. Nakayama S., Sasaki A., Mese H., Alcalde R.E., Matsumura T. Establishment of high and low metastasis cell lines derived from a human tongue squamous cell carcinoma. Invasion Metastasis 1998, 18:219-228.
27. Liu Z., Li S., Cai Y., Wang A., He Q., Zheng C., et al. Manganese superoxide dismutase induces migration and invasion of tongue squamous cell carcinoma via H(2)O(2)-dependent snail signaling. Free Radic Biol Med 2012, 53:44-50.
28. Wang A., Zhang B., Huang H., Zhang L., Zeng D., Tao Q., et al. Suppression of local invasion of ameloblastoma by inhibition of matrix metalloproteinase-2 in vitro. BMC Cancer 2008, 8:182.
29. Ding X., Zhang N., Cai Y., Li S., Zheng C., Jin Y., et al. Down-regulation of tumor suppressor MTUS1/ATIP is associated with enhanced proliferation, poor differentiation and poor prognosis in oral tongue squamous cell carcinoma. Mol Oncol 2012, 6:73-80.
30. Nikkhah M., Strobl J.S., De Vita R., Agah M. The cytoskeletal organization of breast carcinoma and fibroblast cells inside three dimensional (3-D) isotropic silicon microstructures. Biomaterials 2010, 31:4552-4561.
31. White F.H., Jin Y., Yang L. An evaluation of the role of nuclear cytoplasmic ratios and nuclear volume densities as diagnostic indicators in metaplastic, dysplastic and neoplastic lesions of the human cheek. Histol Histopathol 1997, 12:69-77.
32. Acerbi I., Luque T., Gimenez A., Puig M., Reguart N., Farre R., et al. Integrin-specific mechanoresponses to compression and extension probed by cylindrical flat-ended AFM tips in lung cells. PLoS One 2013, 7:e32261.
33. Morita Y., Mukai T., Ju Y., Watanabe S. Evaluation of stem cell-to-tenocyte differentiation by atomic force microscopy to measure cellular elastic moduli. Cell Biochem Biophys 2012, 10.1007/s12013-012-9455-x.
34. Birukova A., Arce F., Moldobaeva N., Dudek S., Garcia J., Lal R., et al. Endothelial permeability is controlled by spatially defined cytoskeletal mechanics: atomic force microscopy force mapping of pulmonary endothelial monolayer. Nanomedicine 2009, 5:30-41.
35. Xu W, Mezencev R, Kim B, Wang L, McDonald J, Sulchek T. Cell stiffness is a biomarker of the metastatic potential of ovarian cancer cells. PLoS ONE; 7: e46609.
36. Ngan A.H.W., Tang B. Response of power-law-viscoelastic and time-dependent materials to rate jumps. Journal of Materials Research 2009, 24:853-862.
37. Tang B., Ngan A.H.W. Nanoindentation measurement of mechanical properties of soft solid covered by a thin liquid film. Soft Materials 2007, 5:169-181.
38. Tang B., Ngan A.H.W., Lu W.W. An improved method for the measurement of mechanical properties of bone by nanoindentation. J Mater Sci Mater Med 2007, 18:1875-1881.
39. Chan B.P., Li C.H., Au-Yeung K.L., Sze K.Y., Ngan A.H.W. A microplate compression method for elastic modulus measurement of soft and viscoelastic collagen microspheres. Ann Biomed Eng 2008, 36:1254-1267.
40. Chan Y.L., Ngan A.H.W. Invariant elastic modulus of viscoelastic materials measured by rate-jump tests. Polym Test 2010, 29:558-564.
41. Fuhrmann A., Staunton J.R., Nandakumar V., Banyai N., Davies P.C., Ros R. AFM stiffness nanotomography of normal, metaplastic and dysplastic human esophageal cells. Phys Biol 2011, 8:015007.
42. Ketene A.N., Schmelz E.M., Roberts P.C., Agah M. The effects of cancer progression on the viscoelasticity of ovarian cell cytoskeleton structures. Nanomedicine 2012, 8:93-102.
43. Sakamoto K., Imanishi Y., Tomita T., Shimoda M., Kameyama K., Shibata K., et al. Overexpression of SIP1 and downregulation of E-cadherin predict delayed neck metastasis in stage I/II oral tongue squamous cell carcinoma after partial glossectomy. Ann Surg Oncol 2012, 19:612-619.
44. Buckley S.T., Medina C., Davies A.M., Ehrhardt C. Cytoskeletal re-arrangement in TGF-β1-induced alveolar epithelial-mesenchymal transition studied by atomic force microscopy and high-content analysis. Nanomedicine 2012, 8:355-364.
45. Kokubo K., Igawa S., Fukuda A., Shinbo T., Hirose M., Masuda N., et al. The role of nitric oxide in reducing deformability of Lewis lung tumor cell stimulated by inflammatory cytokines. Nitric Oxide 2008, 19:312-319.
46. Cai X., Xing X., Cai J., Chen Q., Wu S., Huang F. Connection between biomechanics and cytoskeleton structure of lymphocyte and Jurkat cells: An AFM study. Micron 2010, 41:257-262.
47. Lee S.Y., Zaske A.M., Novellino T., Danila D., Ferrari M., Conyers J., et al. Probing the mechanical properties of TNF-alpha stimulated endothelial cell with atomic force microscopy. Int J Nanomedicine 2011, 6:179-195.
48. González Avalos P., Reichenzeller M., Eils R., Gladilin E. Probing compressibility of the nuclear interior in wild-type and lamin deficient cells using microscopic imaging and computational modeling. J Biomech 2011, 44:2642-2648.
49. Stroka K.M., Aranda-Espinoza H. Effects of morphology vs. cell-cell interactions on endothelial cell stiffness. Cell Mol Bioeng 2011, 4:9-27.