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Fluid Shear Stress Induces Cell Cycle Arrest in Human Urinary Bladder Transitional Cell Carcinoma Through Bone Morphogenetic Protein Receptor-Smad1/5 Pathway

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Abstract

Introduction

Mechanical force generated from the interstitial fluid flow inside and surrounding tissue has been known to play a significant role in cancer pathophysiology. In this study, we aimed to investigate the role of laminar shear stress (LSS) in modulating the cell cycle of human bladder transitional carcinoma (BFTC-905) cells which are frequently stimulated by not only the interstitial fluid flow, but also the urine flow transported from kidney to bladder in the urinary tract.

Methods

The BFTC-905 cells were subjected to 0–12 dynes cm−2 LSS for 1, 4, 8, or 12 h, respectively, followed by cellular and molecular assays for investigations of cell cycle regulation protein expressions, cell growth rates, and the potential mechanism.

Results

The results showed that the LSS with ≥ 8 dynes cm−2 for ≥ 8 h significantly increased protein expressions of cyclin B1, Wee1, p21, and p-CDK1(Tyr15) (p < 0.05 for each), but conversely decreased protein expressions of cyclin A2, D1, E1, and CDK-1, -2, -4, and -6 (p < 0.05 for each) in the BFTC-905 cells, indicating that a G2/M cell cycle arrest was obtained after shearing stimulation. Furthermore, our data demonstrated that the LSS-induced G2/M arrest and the corresponding changes in cell cycle regulatory protein expressions were modulated by bone morphogenetic protein (BMP) receptor-Smad1/5 signaling pathway.

Conclusions

Our findings provided evidences for the effect of mechanical microenvironment on urothelial cancer pathobiology and generated insights into mechanism of LSS-regulated bladder tumor cell cycle.

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References

  1. Allard, P., P. Bernard, Y. Fradet, and B. Têtu. The early clinical course of primary Ta and T1 bladder cancer: a proposed prognostic index. Br. J. Urol. 81(5):692–698, 1998.

    Article  Google Scholar 

  2. Antoni, S., J. Ferlay, I. Soerjomataram, A. Znaor, A. Jemal, and F. Bray. Bladder cancer incidence and mortality: a global overview and recent trends. Eur. Urol. 71(1):96–108, 2017.

    Article  Google Scholar 

  3. Bleuming, S. A., X. C. He, L. L. Kodach, J. C. Hardwick, F. A. Koopman, F. J. Ten Kate, S. J. van Deventer, D. W. Hommes, M. P. Peppelenbosch, G. J. Offerhaus, L. Li, and G. R. van den Brink. Bone morphogenetic protein signaling suppresses tumorigenesis at gastric epithelial transition zones in mice. Cancer Res. 67(17):8149–8155, 2007.

    Article  Google Scholar 

  4. Cai, Z., J. Xin, D. M. Pollock, and J. S. Pollock. Shear stress-mediated NO production in inner medullary collecting duct cells. Am. J. Physiol. Renal Physiol. 279(2):F270–F274, 2000.

    Article  Google Scholar 

  5. Chiu, J. J., and S. Chien. Effects of disturbed flow on vascular endothelium: pathophysiological basis and clinical perspectives. Physiol. Rev. 91(1):327–387, 2011.

    Article  MathSciNet  Google Scholar 

  6. Cohen, S. M., and L. B. Ellwein. Cell proliferation in carcinogenesis. Science 249(4972):1007–1011, 1990.

    Article  Google Scholar 

  7. Den Haese, G. J., N. Walworth, A. M. Carr, K. L. Gould, and K. L. The. Wee1 protein kinase regulates T14 phosphorylation of fission yeast Cdc2. Mol. Biol. Cell. 6(4):371–385, 1995.

    Article  Google Scholar 

  8. Farber, E. Cell proliferation as a major risk factor for cancer: a concept of doubtful validity. Cancer Res. 55(17):3759–3762, 1995.

    Google Scholar 

  9. Graña, X., and E. P. Reddy. Cell cycle control in mammalian cells: role of cyclins, cyclin dependent kinases (CDKs), growth suppressor genes and cyclin-dependent kinase inhibitors (CKIs). Oncogene 11(2):211–219, 1995.

    Google Scholar 

  10. Hofmann, M., M. Guschel, A. Bernd, J. Bereiter-Hahn, R. Kaufmann, C. Tandi, H. Wiig, and S. Kippenberger. Lowering of tumor interstitial fluid pressure reduces tumor cell proliferation in a xenograft tumor model. Neoplasia 8(2):89–95, 2006.

    Article  Google Scholar 

  11. Ikushima, H., and K. Miyazono. TGFbeta signalling: a complex web in cancer progression. Nat. Rev. Cancer 10(6):415–424, 2010.

    Article  Google Scholar 

  12. Jain, R. K., R. T. Tong, and L. L. Munn. Effect of vascular normalization by antiangiogenic therapy on interstitial hypertension, peritumor edema, and lymphatic metastasis: insights from a mathematical model. Cancer Res. 67(6):2729–2735, 2007.

    Article  Google Scholar 

  13. Jemal, A., F. Bray, M. M. Center, J. Ferlay, E. Ward, and D. Forman. Global cancer statistics. CA Cancer J. Clin. 61(2):69–90, 2011.

    Article  Google Scholar 

  14. Jiang, W. G., A. J. Sanders, M. Katoh, H. Ungefroren, F. Gieseler, M. Prince, et al. Tissue invasion and metastasis: molecular, biological and clinical perspectives. Semin. Cancer Biol. 35(Suppl):S244–S275, 2015.

    Article  Google Scholar 

  15. Kim, B. G., C. Li, W. Qiao, M. Mamura, B. Kasprzak, M. Anver, L. Wolfraim, S. Hong, E. Mushinski, M. Potter, S. J. Kim, X. Y. Fu, C. Deng, and J. J. Letterio. Smad4 signaling in T cells is required for suppression of gastrointestinal cancer. Nature 441(7096):1015–1019, 2006.

    Article  Google Scholar 

  16. Kuo, C. C., H. P. Hsieh, W. Y. Pan, C. P. Chen, J. P. Liou, S. J. Lee, Y. L. Chang, L. T. Chen, C. T. Chen, and J. Y. Chang. BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo. Cancer Res. 64(13):4621–4628, 2004.

    Article  Google Scholar 

  17. Lee, H. J., A. Ewere, M. F. Diaz, and P. L. Wenzel. TAZ responds to fluid shear stress to regulate the cell cycle. Cell Cycle 16:1–21, 2017.

    Article  Google Scholar 

  18. Lee, Y. H., C. C. Lee, C. H. Huang, and F. M. Ho. Laminar shear stress promotes nicotine-induced inflammation and hemostatic expression in human endothelial cells. Cell. Mol. Bioeng. 9(3):466–477, 2016.

    Article  Google Scholar 

  19. Manoharan, M. Intravesical therapy for urothelial carcinoma of the bladder. Indian J. Urol. 27(2):252–261, 2011.

    Article  Google Scholar 

  20. Mitra, A. P., D. I. Quinn, T. B. Dorff, E. C. Skinner, A. K. Schuckman, G. Miranda, I. S. Gill, and S. Daneshmand. Factors influencing post-recurrence survival in bladder cancer following radical cystectomy. BJU Int. 109(6):846–854, 2012.

    Article  Google Scholar 

  21. Motoshima, H., B. J. Goldstein, M. Igata, and E. Araki. AMPK and cell proliferation—AMPK as a therapeutic target for atherosclerosis and cancer. J. Physiol. 574(Pt 1):63–71, 2006.

    Article  Google Scholar 

  22. Nerem, R. M. Tissue engineering: the hope, the hype, and the future. Tissue Eng. 12(5):1143–1150, 2006.

    Article  Google Scholar 

  23. Netti, P. A., L. T. Baxter, Y. Boucher, R. Skalak, and R. K. Jain. Time-dependent behavior of interstitial fluid pressure in solid tumors: implications for drug delivery. Cancer Res. 55(22):5451–5458, 1995.

    Google Scholar 

  24. Netti, P. A., L. M. Hamberg, J. W. Babich, D. Kierstead, W. Graham, G. J. Hunter, G. L. Wolf, A. Fischman, Y. Boucher, and R. K. Jain. Enhancement of fluid filtration across tumor vessels: implication for delivery of macromolecules. Proc. Natl Acad. Sci. U.S.A. 96(6):3137–3142, 1999.

    Article  Google Scholar 

  25. Rutkowski, J. M., and M. A. Swartz. A driving force for change: interstitial flow as a morphoregulator. Trends Cell Biol. 17(1):44–50, 2007.

    Article  Google Scholar 

  26. Shin, S. Y., Y. Yong, C. G. Kim, Y. H. Lee, and Y. Lim. Deoxypodophyllotoxin induces G2/M cell cycle arrest and apoptosis in HeLa cells. Cancer Lett. 287(2):231–239, 2010.

    Article  Google Scholar 

  27. Siegel, R. L., K. D. Miller, and A. Jemal. Cancer statistics, 2016. CA Cancer J. Clin. 66(1):7–30, 2016.

    Article  Google Scholar 

  28. Tarbell, J. M., and Z. D. Shi. Effect of the glycocalyx layer on transmission of interstitial flow shear stress to embedded cells. Biomech. Model. Mechanobiol. 12(1):111–121, 2013.

    Article  Google Scholar 

  29. Xiong, N., S. Li, K. Tang, H. Bai, Y. Peng, H. Yang, C. Wu, and Y. Liu. Involvement of caveolin-1 in low shear stress-induced breast cancer cell motility and adhesion: roles of FAK/Src and ROCK/p-MLC pathways. Biochim. Biophys. Acta. 1864(1):12–22, 2017.

    Article  Google Scholar 

  30. Yu, P. B., C. C. Hong, C. Sachidanandan, J. L. Babitt, D. Y. Deng, S. A. Hoyng, H. Y. Lin, K. D. Bloch, and R. T. Peterson. Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat. Chem. Biol. 4(1):33–41, 2008.

    Article  Google Scholar 

  31. Zhou, J., P. L. Lee, C. I. Lee, S. Y. Wei, S. H. Lim, T. E. Lin, S. Chien, and J. J. Chiu. BMP receptor-integrin interaction mediates responses of vascular endothelial Smad1/5 and proliferation to disturbed flow. J. Thromb. Haemost. 11(4):741–755, 2013.

    Article  Google Scholar 

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Acknowledgments

This work was financially supported by Ministry of Science and Technology, Taiwan R.O.C. (MOST 106-2221-E-008-060; Y.-H. Lee and MOST 106-2314-B-281-001-MY3; Y.-C. Cheng).

CONFLICT OF INTEREST

Yu-Hsiang Lee, Chia-Wei Lai, and Yu-Che Cheng declare no conflict of interest.

COMPLICANCE WITH ETHICAL STANDARDS

This article does not contain any studies with human participants or animals performed by any of the authors.

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Correspondence to Yu-Hsiang Lee or Yu-Che Cheng.

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Associate Editor Partha Roy oversaw the review of this article.

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Lee, YH., Lai, CW. & Cheng, YC. Fluid Shear Stress Induces Cell Cycle Arrest in Human Urinary Bladder Transitional Cell Carcinoma Through Bone Morphogenetic Protein Receptor-Smad1/5 Pathway. Cel. Mol. Bioeng. 11, 185–195 (2018). https://doi.org/10.1007/s12195-018-0523-1

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