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Published in: Journal of Experimental & Clinical Cancer Research 1/2010

Open Access 01-12-2010 | Research

Effect of all-trans retinoic acid on the proliferation and differentiation of brain tumor stem cells

Authors: Chao Shi Niu, Ming Wu Li, Yong Feng Ni, Jian Min Chen, Jia Ming Mei, Jing Li, Xian Ming Fu

Published in: Journal of Experimental & Clinical Cancer Research | Issue 1/2010

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Abstract

Objective

To investigate the effect of all-trans retinoic acid(ATRA) on the proliferation and differentiation of brain tumor stem cells(BTSCs) in vitro.

Methods

Limiting dilution and clonogenic assay were used to isolate and screen BTSCs from the fresh specimen of human brain glioblastoma. The obtained BTSCs, which were cultured in serum-free medium, were classified into four groups in accordance with the composition of the different treatments. The proliferation of the BTSCs was evaluated by MTT assay. The BTSCs were induced to differentiate in serum-containing medium, and classified into the ATRA group and control group. On the 10th day of induction, the expressions of CD133 and glial fibrillary acidic protein (GFAP) in the differentiated BTSCs were detected by immunofluorescence. The differentiated BTSCs were cultured in serum-free medium, the percentage and the time required for formation of brain tumor spheres (BTS) were observed.

Results

BTSCs obtained by limiting dilution were all identified as CD133-positive by immunofluorescence. In serum-free medium, the proliferation of BTSCs in the ATRA group was observed significantly faster than that in the control group, but slower than that in the growth factor group and ATRA/growth factor group, and the size of the BTS in the ATRA group was smaller than that in the latter two groups(P < 0.01). In serum-containing medium, the expression percentages of CD133 and GFAP in the differentiated BTSCs were (2.29% ± 0.27%) and (75.60% ± 4.03%) respectively in the ATRA group, and (7.05% ± 0.49%) and (12.51% ± 0.77%) respectively in the control group. The differentiation rate of BTSCs in the ATRA group was significantly higher than that in the control group (P < 0.05), but there was still CD133 expressed in the ATRA group. The differentiated BTSCs could re-form BTSs in serum-free medium. The percentage of BTS formation in the ATRA group was(4.84% ± 0.32%), significantly lower than that in the control group (17.71% ± 0.78%) (P < 0.05), and the time required for BTS formation in the ATRA group was (10.07 ± 1.03)d, significantly longer than that in the control group (4.08 ± 0.35)d (P < 0.05).

Conclusion

ATRA can promote the proliferation and induce the differentiation of BTSCs, but the differentiation is incomplete, terminal differentiation cannot be achieved and BTSs can be formed again.
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Literature
1.
go back to reference Haque A, Banik NL, Ray SK: Emerging role of combination of all-trans retinoic acid and interferon-gamma as chemoimmunotherapy in the management of human glioblastoma[J]. Neurochem Res. 2007, 32 (12): 2203-2209. 10.1007/s11064-007-9420-z.CrossRef Haque A, Banik NL, Ray SK: Emerging role of combination of all-trans retinoic acid and interferon-gamma as chemoimmunotherapy in the management of human glioblastoma[J]. Neurochem Res. 2007, 32 (12): 2203-2209. 10.1007/s11064-007-9420-z.CrossRef
2.
go back to reference Che XM, Cui DM, Wang Y, Shi W, Liu TJ, Wang K: Isolation, Culture and Identification and Biological Character Research of Brain Tumor Stem Cells in Glioblastoma Multiforme in Vitro [J]. Chinese Journal of Clinical Neurosciences. 2007, 15 (6): 561-569. Che XM, Cui DM, Wang Y, Shi W, Liu TJ, Wang K: Isolation, Culture and Identification and Biological Character Research of Brain Tumor Stem Cells in Glioblastoma Multiforme in Vitro [J]. Chinese Journal of Clinical Neurosciences. 2007, 15 (6): 561-569.
3.
go back to reference Singh SK, Clarke ID, Terasaki M, Bonn VE, Hawkins C, Squire J, Dirks PB: Identification of a cancer stem cell in human brain tumors[J]. Cancer Res. 2003, 63 (18): 5821-5828. Singh SK, Clarke ID, Terasaki M, Bonn VE, Hawkins C, Squire J, Dirks PB: Identification of a cancer stem cell in human brain tumors[J]. Cancer Res. 2003, 63 (18): 5821-5828.
4.
go back to reference Galli R, Binda E, Orfanelli U, Cipelletti B, Gritti A, Vitis SD, Fiocco R, Foroni C, Dimeco F, Vescovi A: Isolation and characterization of tumorigenic, stem-like neural precursors from human glioblastoma[J]. Cancer Res. 2004, 64 (19): 7011-7021. 10.1158/0008-5472.CAN-04-1364.CrossRef Galli R, Binda E, Orfanelli U, Cipelletti B, Gritti A, Vitis SD, Fiocco R, Foroni C, Dimeco F, Vescovi A: Isolation and characterization of tumorigenic, stem-like neural precursors from human glioblastoma[J]. Cancer Res. 2004, 64 (19): 7011-7021. 10.1158/0008-5472.CAN-04-1364.CrossRef
5.
go back to reference Singh SK, Hawkins C, Clarke ID, Squire JA, Bayani J, Hide T, Henkelman RM, Cusimano MD, Dirks PB: Identification of human brain tumour initiating cells[J]. Nature. 2004, 432 (7015): 396-401. 10.1038/nature03128.CrossRef Singh SK, Hawkins C, Clarke ID, Squire JA, Bayani J, Hide T, Henkelman RM, Cusimano MD, Dirks PB: Identification of human brain tumour initiating cells[J]. Nature. 2004, 432 (7015): 396-401. 10.1038/nature03128.CrossRef
6.
go back to reference Kondo T, Setoguchi T, Taga T: Persistence of a small subpopulation of cancer stem-like cells in the C6 glioma cell line[J]. Proc Natl Acad Sci USA. 2004, 101 (3): 781-786. 10.1073/pnas.0307618100.CrossRef Kondo T, Setoguchi T, Taga T: Persistence of a small subpopulation of cancer stem-like cells in the C6 glioma cell line[J]. Proc Natl Acad Sci USA. 2004, 101 (3): 781-786. 10.1073/pnas.0307618100.CrossRef
7.
go back to reference Zang C, Wächter M, Liu H, Posch MG, Fenner MH, Stadelmann C, von Deimling A, Possinger K, Black KL, Koeffler HP, Elstner E: Ligands for PPARgamma and RAR cause induction of growth inhibition and apoptosis in human glioblastomas[J]. J Neurooncol. 2003, 65 (2): 107-118. 10.1023/B:NEON.0000003728.80052.a8.CrossRef Zang C, Wächter M, Liu H, Posch MG, Fenner MH, Stadelmann C, von Deimling A, Possinger K, Black KL, Koeffler HP, Elstner E: Ligands for PPARgamma and RAR cause induction of growth inhibition and apoptosis in human glioblastomas[J]. J Neurooncol. 2003, 65 (2): 107-118. 10.1023/B:NEON.0000003728.80052.a8.CrossRef
8.
go back to reference Kaba SE, Kyritsis AP, Conrad C, Gleason MJ, Newman R, Levin VA, Yung WK: The treatment of recurrent cerebral gliomas with all-trans-retinoic acid (tretinoin)[J]. J Neurooncol. 1997, 34 (2): 145-151. 10.1023/A:1005743707803.CrossRef Kaba SE, Kyritsis AP, Conrad C, Gleason MJ, Newman R, Levin VA, Yung WK: The treatment of recurrent cerebral gliomas with all-trans-retinoic acid (tretinoin)[J]. J Neurooncol. 1997, 34 (2): 145-151. 10.1023/A:1005743707803.CrossRef
9.
go back to reference Phuphanich S, Scott C, Fischbach AJ, Langer C, Yung WK: All-trans-retinoic acid: a phase II Radiation Therapy Oncology Group study(RTOG 91-13) in patients with recurrent malignant astrocytoma[J]. J Neurooncol. 1997, 34 (2): 193-200. 10.1023/A:1005765915288.CrossRef Phuphanich S, Scott C, Fischbach AJ, Langer C, Yung WK: All-trans-retinoic acid: a phase II Radiation Therapy Oncology Group study(RTOG 91-13) in patients with recurrent malignant astrocytoma[J]. J Neurooncol. 1997, 34 (2): 193-200. 10.1023/A:1005765915288.CrossRef
10.
go back to reference Engelhard HH, Duncan HA, Del Canto M: Molecular characterization of glioblastoma cell differentiation[J]. Neurosurgery. 1997, 41 (4): 886-896. 10.1097/00006123-199710000-00023.CrossRef Engelhard HH, Duncan HA, Del Canto M: Molecular characterization of glioblastoma cell differentiation[J]. Neurosurgery. 1997, 41 (4): 886-896. 10.1097/00006123-199710000-00023.CrossRef
11.
go back to reference Toda M, Miura M, Asou H, Toya S, Uyemura K: Cell growth suppression of astrocytoma C6 cells by glial fibrillary acidic protein cDNA transfection[J]. J Neurochem. 1994, 63 (5): 1975-1978. 10.1046/j.1471-4159.1994.63051975.x.CrossRef Toda M, Miura M, Asou H, Toya S, Uyemura K: Cell growth suppression of astrocytoma C6 cells by glial fibrillary acidic protein cDNA transfection[J]. J Neurochem. 1994, 63 (5): 1975-1978. 10.1046/j.1471-4159.1994.63051975.x.CrossRef
12.
go back to reference Kokunai T, Izawa I, Tamaki N: Overexpression of p21WAF1/CIP1 induces cell differentiation and growth inhibition in a human glioma cell line[J]. Int J Cancer. 1998, 75 (4): 643-648. 10.1002/(SICI)1097-0215(19980209)75:4<643::AID-IJC24>3.0.CO;2-8.CrossRef Kokunai T, Izawa I, Tamaki N: Overexpression of p21WAF1/CIP1 induces cell differentiation and growth inhibition in a human glioma cell line[J]. Int J Cancer. 1998, 75 (4): 643-648. 10.1002/(SICI)1097-0215(19980209)75:4<643::AID-IJC24>3.0.CO;2-8.CrossRef
13.
go back to reference Yuan X, Curtin J, Xiong Y, Liu G, Waschsmann-Hogiu S, Farkas DL, Black KL, Yu JS: Isolation of cancer stem cells from adult glioblastoma multiforme[J]. Oncogene. 2004, 23 (58): 9392-9400. 10.1038/sj.onc.1208311.CrossRef Yuan X, Curtin J, Xiong Y, Liu G, Waschsmann-Hogiu S, Farkas DL, Black KL, Yu JS: Isolation of cancer stem cells from adult glioblastoma multiforme[J]. Oncogene. 2004, 23 (58): 9392-9400. 10.1038/sj.onc.1208311.CrossRef
Metadata
Title
Effect of all-trans retinoic acid on the proliferation and differentiation of brain tumor stem cells
Authors
Chao Shi Niu
Ming Wu Li
Yong Feng Ni
Jian Min Chen
Jia Ming Mei
Jing Li
Xian Ming Fu
Publication date
01-12-2010
Publisher
BioMed Central
Published in
Journal of Experimental & Clinical Cancer Research / Issue 1/2010
Electronic ISSN: 1756-9966
DOI
https://doi.org/10.1186/1756-9966-29-113

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