Hostname: page-component-669899f699-cf6xr Total loading time: 0 Render date: 2025-04-28T01:20:44.524Z Has data issue: false hasContentIssue false
  • English
  • Français

An in vitro model of prostate cancer bone metastasis for highly metastatic and non-metastatic prostate cancer using nanoclay bone-mimetic scaffolds

Published online by Cambridge University Press:  03 January 2019

MD Shahjahan Molla ,
Dinesh R. Katti  and
Kalpana S. Katti
MD Shahjahan Molla
Affiliation:
Civil and Environmental Engineering, North Dakota State University, Fargo, ND58108, USA
Dinesh R. Katti*
Affiliation:
Civil and Environmental Engineering, North Dakota State University, Fargo, ND58108, USA
Kalpana S. Katti*
Affiliation:
Civil and Environmental Engineering, North Dakota State University, Fargo, ND58108, USA
*
*(Email: [email protected])
Get access

Abstract

Prostate cancer has a strong preference for metastasizing to bone which is the primary cause of prostate cancer-related morbidity and mortality. The complex nature of cancer metastasis requires the development of translational models that recapitulate a specific metastatic stage. Herein, we report the mimicking of mesenchymal to epithelial transition (MET) of prostate cancer cells using highly metastatic and a non-metastatic prostate cancer cell lines. A unique cell culture technique that we termed as ‘sequential culture’ was used to create a biomimetic bone microenvironment for metastasized prostate cancer cells by introducing bioactive factors from osteogenic induction of human mesenchymal stem cells (MSCs) within the porous 3D scaffolds. The in vitro 3D tumor model can be used as a testbed to study the interaction between prostate cancer and bone microenvironment and for the design of novel therapeutic studies.

Keywords

biomaterialbiomedicalbiomimeticbonecomposite
Type
Articles
Information
MRS Advances , Volume 4 , Issue 21: Biomaterials and Soft Materials , 2019 , pp. 1207 - 1213
Copyright
Copyright © Materials Research Society 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Article purchase

Temporarily unavailable

References

REFERENCES

Noone, A.M., Howlader, N., Krapcho, M., Miller, D., Brest, A., Yu, M., Ruhl, J., Tatalovich, Z., Mariotto, A., Lewis, D.R., Chen, H.S., Feuer, E.J., Cronin, K.A., SEER Cancer Statistics Review, 1975-2015, (National Cancer Institute. Bethesda, MD, 2018).Google Scholar
Molla, M.S., Katti, D.R., and Katti, K.S., Journal of Tissue Engineering and Regenerative Medicine 12 (3), 727 (2017).CrossRefGoogle Scholar
Katti, K.S., Molla, M.S., Karandish, F., Haldar, M.K., Mallik, S., and Katti, D.R., Journal of Biomedical Materials Research Part A 104 (7), 1591 (2016).CrossRefGoogle Scholar
Katti, K.S., Katti, D.R., Molla, M.S., and Kar, S., in Poromechanics VI, pp. 881.Google Scholar
Ambre, A.H., Katti, D.R., and Katti, K.S., Journal of Biomedical Materials Research Part A 103 (6), 2077 (2015).CrossRefGoogle Scholar
Ambre, A.H., Katti, K.S., and Katti, D.R., Journal of Nanotechnology in Engineering and Medicine 1 (3), 031013 (2010);CrossRefGoogle Scholar
Ambre, A.H., Katti, K.S., and Katti, D.R., Materials Science and Engineering: C 31 (5), 1017 (2011).CrossRefGoogle Scholar
Katti, K.S., Ambre, A.H., Peterka, N., and Katti, D.R., Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 368 (1917), 1963 (2010).CrossRefGoogle Scholar
Ambre, A.H., Katti, D.R., and Katti, K.S., Journal of Biomedical Materials Research Part A 101A (9), 2644 (2013).CrossRefGoogle Scholar
Chaffer, C.L. and Weinberg, R.A., Science 331 (6024), 1559 (2011).CrossRefGoogle Scholar
Katti, D.R., Katti, K.S., Molla, M.S., and Kar, S., in Encyclopedia of Biomedical Engineering, edited by Narayan, Roger (Elsevier, Oxford, 2019), pp. 1.Google Scholar