#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Induction of neural differentiation in rat C6 glioma cells with taxol


Background:
Glioblastoma is a common and aggressive type of primary brain tumor. Several anticancer drugs affect GBM (glioblastoma multiforme) cells on cell growth and morphology. Taxol is one of the widely used antineoplastic drugs against many types of solid tumors, such as breast, ovarian, and prostate cancers. However, the effect of taxol on GBM cells remains unclear and requires further investigation.

Methods:
Survival rate of C6 glioma cells under different taxol concentrations was quantified. To clarify the differentiation patterns of rat C6 glioma cells under taxol challenge, survived glioma cells were characterized by immunocytochemical, molecular biological, and cell biological approaches.

Results:
After taxol treatment, not only cell death but also morphological changes, including cell elongation, cellular processes thinning, irregular shapes, and fragmented nucleation or micronuclei, occurred in the survived C6 cells. Neural differentiation markers NFL (for neurons), βIII-tubulin (for neurons), GFAP (for astrocytes), and CNPase (for oligodendrocytes) were detected in the taxol-treated C6 cells. Quantitative analysis suggested a significant increase in the percentage of neural differentiated cells. The results exhibited that taxol may trigger neural differentiation in C6 glioma cells. Increased expression of neural differentiation markers in C6 cells after taxol treatment suggest that some anticancer drugs could be applied to elimination of the malignant cancer cells as well as changing proliferation and differentiation status of tumor cells.

Keywords:
Glioma; neural differentiation; taxol


Autoři: Chuan-Chuan Chao 1;  †;  Daphne Kan 2;  †;  Ta-Hsuan Lo 2;  Kuo-Shyan Lu Andchung-Liang Chien 1 1,2,*
Působiště autorů: Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, Taipei, Taiwan 1;  Center of Genomic Medicine, National Taiwan University, Taipei, Taiwan 2
Vyšlo v časopise: Brain and Behavior, Early View, 2015, č. Early View, s. 1-10
prolekare.web.journal.doi_sk: https://doi.org/10.1002/brb3.414

© 2015 The Authors. Brain and Behavior published by Wiley Periodicals, Inc.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Souhrn

Background:
Glioblastoma is a common and aggressive type of primary brain tumor. Several anticancer drugs affect GBM (glioblastoma multiforme) cells on cell growth and morphology. Taxol is one of the widely used antineoplastic drugs against many types of solid tumors, such as breast, ovarian, and prostate cancers. However, the effect of taxol on GBM cells remains unclear and requires further investigation.

Methods:
Survival rate of C6 glioma cells under different taxol concentrations was quantified. To clarify the differentiation patterns of rat C6 glioma cells under taxol challenge, survived glioma cells were characterized by immunocytochemical, molecular biological, and cell biological approaches.

Results:
After taxol treatment, not only cell death but also morphological changes, including cell elongation, cellular processes thinning, irregular shapes, and fragmented nucleation or micronuclei, occurred in the survived C6 cells. Neural differentiation markers NFL (for neurons), βIII-tubulin (for neurons), GFAP (for astrocytes), and CNPase (for oligodendrocytes) were detected in the taxol-treated C6 cells. Quantitative analysis suggested a significant increase in the percentage of neural differentiated cells. The results exhibited that taxol may trigger neural differentiation in C6 glioma cells. Increased expression of neural differentiation markers in C6 cells after taxol treatment suggest that some anticancer drugs could be applied to elimination of the malignant cancer cells as well as changing proliferation and differentiation status of tumor cells.

Keywords:
Glioma; neural differentiation; taxol


Zdroje

1. Abramovitch, R., G. Meir, and M. Neeman. 1995. Neovascularization induced growth of implanted C6 glioma multicellular spheroids: magnetic resonance microimaging. Cancer Res. 55:1956–1962.

2. Auer, R. N., R. F. Del Maestro, and R. Anderson. 1981. A simple and reproducible experimental in vivo glioma model. Can. J. Neurol. Sci. 8:325–331.

3. Benda, P., J. Lightbody, G. Sato, L. Levine, and W. Sweet. 1968. Differentiated rat glial cell strain in tissue culture. Science161:370–371.

4. Bernstein, J. J., W. J. Goldberg, E. R. Jr Laws, D. Conger, V. Morreale, and L. R. Wood. 1990. C6 glioma cell invasion and migration of rat brain after neural homografting: ultrastructure. Neurosurgery 26:622–628.

5. Bernstein, J. J., E. R. Jr Laws, K. V. Levine, L. R. Wood, G. Tadvalkar, and W. J. Goldberg. 1991. C6 glioma-astrocytoma cell and fetal astrocyte migration into artificial basement membrane: a permissive substrate for neural tumors but not fetal astrocytes.Neurosurgery 28:652–658.

6. Bianchi, M. G., G. C. Gazzola, L. Tognazzi, and O. Bussolati. 2008. C6 glioma cells differentiated by retinoic acid overexpress the glutamate transporter excitatory amino acid carrier 1 (EAAC1). Neuroscience 151:1042–1052.. Herman, A. Frankfurter, V. P. Collins, and L. J. Rubinstein. 1989. Immunohistochemistry of a spontaneous murine ovarian teratoma with neuroepithelial differentiation. Neuron-associated beta-tubulin as a marker for primitive neuroepithelium. Lab. Invest. 60:390–398.

7. Chicoine, M. R., and D. L. Silbergeld. 1995. Invading C6 glioma cells maintaining tumorigenicity. J. Neurosurg. 83:665–671.

8. Das, G. C., D. Holiday, R. Gallardo, and C. Haas. 2001. Taxol-induced cell cycle arrest and apoptosis: dose-response relationship in lung cancer cells of different wild-type p53 status and under isogenic condition. Cancer Lett. 165:147–153.

9. Goetschy, J. F., G. Ulrich, D. Aunis, and J. Ciesielski-Treska. 1986. The organization and solubility properties of intermediate filaments and microtubules of cortical astrocytes in culture. J. Neurocytol. 15:375–387.

10. Hari, M., H. Yang, C. Zeng, M. Canizales, and F. Cabral. 2003. Expression of class III beta-tubulin reduces microtubule assembly and confers resistance to paclitaxel. Cell Motil. Cytoskeleton 56:45–56.

11. Horwitz, S. B. 1994. Taxol (paclitaxel): mechanisms of action. Ann. Oncol. 5(Suppl 6):S3–S6.

12. Hu, W., T. Onuma, N. Birukawa, M. Abe, E. Ito, Z. Chen, et al. 2008. Change of morphology and cytoskeletal protein gene expression during dibutyryl cAMP-induced differentiation in C6 glioma cells. Cell. Mol. Neurobiol. 28:519–528.

13. Jia, L., S. Zhang, Y. Ye, X. Li, I. Mercado-Uribe, R. C. Jr Bast, et al. 2012. Paclitaxel inhibits ovarian tumor growth by inducing epithelial cancer cells to benign fibroblast-like cells. Cancer Lett. 326:176–182.

14. Karmakar, S., N. L. Banik, and S. K. Ray. 2008. Combination of all-trans retinoic acid and paclitaxel-induced differentiation and apoptosis in human glioblastoma U87MG xenografts in nude mice. Cancer 112:596–607.

15. Katsetos, C. D., A. Legido, E. Perentes, and S. J. Mork. 2003. Class III beta-tubulin isotype: a key cytoskeletal protein at the crossroads of developmental neurobiology and tumor neuropathology. J. Child Neurol. 18:851–866; discussion 867.

16. Katsetos, C. D., E. Draberova, B. Smejkalova, G. Reddy, L. Bertrand, J. P. de Chadarevian, et al. 2007. Class III beta-tubulin and gamma-tubulin are co-expressed and form complexes in human glioblastoma cells. Neurochem. Res. 32:1387–1398.

17. Kavallaris, M. 2010. Microtubules and resistance to tubulin-binding agents. Nat. Rev. Cancer 10:194–204.

18. Kavallaris, M., D. Y. Kuo, C. A. Burkhart, D. L. Regl, M. D. Norris, M. Haber, et al. 1997. Taxol-resistant epithelial ovarian tumors are associated with altered expression of specific beta-tubulin isotypes. J. Clin. Invest. 100:1282–1293.

19. Kavallaris, M., C. A. Burkhart, and S. B. Horwitz. 1999. Antisense oligonucleotides to class III beta-tubulin sensitize drug-resistant cells to Taxol. Br. J. Cancer 80:1020–1025.

20. Lange, A., H. Gustke, G. Glassmeier, M. Heine, U. Zangemeister-Wittke, J. R. Schwarz, et al. 2011. Neuronal differentiation by indomethacin and IBMX inhibits proliferation of small cell lung cancer cells in vitro. Lung Cancer 74:178–187.

21. Lariviere, R. C., and J. P. Julien. 2004. Functions of intermediate filaments in neuronal development and disease. J. Neurobiol.58:131–148.

22. Lee, K. M., D. Cao, A. Itami, P. M. Pour, R. H. Hruban, A. Maitra, et al. 2007. Class III beta-tubulin, a marker of resistance to paclitaxel, is overexpressed in pancreatic ductal adenocarcinoma and intraepithelial neoplasia. Histopathology 51:539–546.

23. Lim, J. S., M. Yoo, H. J. Kwon, H. Kim, and Y. K. Kwon. 2010. Wogonin induces differentiation and neurite outgrowth of neural precursor cells. Biochem. Biophys. Res. Commun. 402:42–47.

24. McMorris, F. A. 1977. Norepinephrine induces glial-specific enzyme activity in cultured plasma glioma cells. Proc. Natl Acad. Sci. USA74:4501–4504.

25. McMorris, F. A. 1983. Cyclic AMP induction of the myelin enzyme 2′,3′-cyclic nucleotide 3′-phosphohydrolase in rat oligodendrocytes.J. Neurochem. 41:506–515.

26. Messens, J., and H. Slegers. 1992. Synthesis of glial fibrillary acidic protein in rat C6 glioma in chemically defined medium: cyclic AMP-dependent transcriptional and translational regulation. J. Neurochem. 58:2071–2080.

27. Michels, T., G. V. Shurin, H. Naiditch, A. Sevko, V. Umansky, and M. R. Shurin. 2012. Paclitaxel promotes differentiation of myeloid-derived suppressor cells into dendritic cells in vitro in a TLR4-independent manner. J. Immunotoxicol. 9:292–300.

28. Nagano, N., H. Sasaki, M. Aoyagi, and K. Hirakawa. 1993. Invasion of experimental rat brain tumor: early morphological changes following microinjection of C6 glioma cells. Acta Neuropathol. 86:117–125.

29. Pushkarev, V. M., D. V. Starenki, V. A. Saenko, H. Namba, J. Kurebayashi, M. D. Tronko, et al. 2004. Molecular mechanisms of the effects of low concentrations of taxol in anaplastic thyroid cancer cells. Endocrinology 145:3143–3152.

30. Ranganathan, S., D. W. Dexter, C. A. Benetatos, A. E. Chapman, K. D. Tew, and G. R. Hudes. 1996. Increase of beta(III)- and beta(IVa)-tubulin isotopes in human prostate carcinoma cells as a result of estramustine resistance. Cancer Res. 56:2584–2589.

31. Ranganathan, S., D. W. Dexter, C. A. Benetatos, and G. R. Hudes. 1998. Cloning and sequencing of human betaIII-tubulin cDNA: induction of betaIII isotype in human prostate carcinoma cells by acute exposure to antimicrotubule agents. Biochim. Biophys. Acta1395:237–245.

32. San-Galli, F., P. Vrignaud, J. Robert, J. M. Coindre, and F. Cohadon. 1989. Assessment of the experimental model of transplanted C6 glioblastoma in Wistar rats. J. Neurooncol. 7:299–304.

33. Schmidek, H. H., S. L. Nielsen, A. L. Schiller, and J. Messer. 1971. Morphological studies of rat brain tumors induced by N-nitrosomethylurea. J. Neurosurg. 34:335–340.

34. Svendsen, C. N., A. Bhattacharyya, and Y. T. Tai. 2001. Neurons from stem cells: preventing an identity crisis. Nat. Rev. Neurosci.2:831–834.

35. Takanaga, H., T. Yoshitake, S. Hara, C. Yamasaki, and M. Kunimoto. 2004. cAMP-induced astrocytic differentiation of C6 glioma cells is mediated by autocrine interleukin-6. J. Biol. Chem. 279:15441–15447.

36. Umezu, T., K. Shibata, H. Kajiyama, M. Terauchi, K. Ino, A. Nawa, et al. 2008. Taxol resistance among the different histological subtypes of ovarian cancer may be associated with the expression of class III beta-tubulin. Int. J. Gynecol. Pathol. 27:207–212.

37. Wu, Y., D. Shen, Z. Chen, S. Clayton, and J. V. Vadgama. 2007. Taxol induced apoptosis regulates amino acid transport in breast cancer cells. Apoptosis 12:593–612.

38. Xiao, H., P. Verdier-Pinard, N. Fernandez-Fuentes, B. Burd, R. Angeletti, A. Fiser, et al. 2006. Insights into the mechanism of microtubule stabilization by Taxol. Proc. Natl Acad. Sci. USA 103:10166–10173.

39. Yoshimura, S., H. Sakai, S. Nakashima, Y. Nozawa, J. Shinoda, N. Sakai, et al. 1997. Differential expression of Rho family GTP-binding proteins and protein kinase C isozymes during C6 glial cell differentiation. Brain Res. Mol. Brain Res. 45:90–98.

40. Zhuang, W., B. Li, L. Long, L. Chen, Q. Huang, and Z. Liang. 2011. Induction of autophagy promotes differentiation of glioma-initiating cells and their radiosensitivity. Int. J. Cancer 129:2720–2731.

Štítky
Neurológia
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#