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1 Progress in Modern Biomedicine 2009 Vol.9 No.1 5 MG-63 * MG-63 1μmol/L MG-63 MG-63 7 MG % G0/G % c-myc c-fos Rb p27 1μmol/L c-myc c-fos Rb p27 :MG-63 Q254, Q279 A Effects of Retinoic Acid on Proliferation and Associated Gene Expression of Human Osteosarcoma MG-63 Cells* SONG Jian-ye, ZHAO Yan, Li Qi-Fu, SHI Song-lin, ZHAO Zhen-li, JING Guang-jun Laboratory of Cell Biolog, School of Life Sciences, Xiamen University, Xiamen, , China ABSTRACT Objective: To explore effect of Retinoic Acid (RA) on proliferation of human osteosarcoma MG-63 cells and its mechanism of antitumor. Methods: The MG-63 cells treated by 1μmol/L RA were subjected to growth curve counts, flow sytometry, immuncocytochemical assay and light microscopy. We investigated the influence of RA on proliferation, cell cycle, expression of associated oncogene and tumor suppressor gene of MG-63 cells. Then we analyzed the mechanism of RA in inducing differentiation primarily. Results: Seven days after treated by 1 μmol/l RA, the inhibition rate of proliferation of MG-63 cells amounted to 42.2 % and RA reduced the rate of progression from G1 to S phase. The cells tend to be flat and spread. Meanwhile, the expression level of oncogene was downregulated and the expression level of tumor suppressor gene was upregulated. Conclusions: 1μmol/L RA could inhibit proliferation of MG-63 cells, reverse the malignant phenotype characters, downregulate expression of Oncogene c-myc, c-fos and upregulate expression of Tumor Suppressor Gene Rb, p27, as a result, induce MG-63 cells into differentiation effectively. Key words: Human Osteosarcoma Cell MG-63; RA; Proliferation; Oncogene; Tumor Suppressor Gene Chinese Library Classification: Q254,Q279 Aticle ID: Document code: A HMBA [2-3] MG-63 retinoic acid RA MG-63 MG [1] MG-63 * Tel songjye123@163.com chifulee@xmu.edu.cn

2 6 Progress in Modern Biomedicine 2009 Vol.9 No.1 RPMI % 100 U/ml 100 ug/ml 50 ug/ml PH MG retinoic acid RA MG-63 Sigma 1 mmol/ml 0.22 μm /ml 4 MG-63 RA /ml 15.6 RA RA /ml 9 1μmol/L MG /ml Table 1 The effect of RA on inhibition of the proliferation of MG-63 cells 2 ml 25 ml h 10 4 /ml group/date 1μmol/L RA Inhibition rate C RA RA Trypan Blue / 42.2 % /ml 24 h 1μmol/L RA 7 d PBS ml PBS 5 ml 70 % 0.1M PBS 3 DNase 100 μg/ml RNaseA PBS 0.5 ml min RNA 50 ug/ml (PI) 4 30 min 1 MG-63 Fig. 1 The effect of RA on the proliferation of human osteosarcoma 1.4 MG-63 cells 1μmol/L RA 5 d /ml RA MG h PBS 2-3 MG-63 G 0 /G % Bouin-Hollande 70 % HE RA G 0 /G % Olympus BH-2 S G2/M 1.5 c-myc c-fos Rb p27 2 MG-63 RA 37 PBS 4 20 min PBS 3 % H 2 O RA MG % Table 2 The influence of RA on the cell cycle of MG-63 Group G 0 /G 1 (%) S(%) G2/M(%) 10 min 2 %BSA 25 min Control c-myc c-fos Rb P27 c-myc RA c-fos P27 Rb 4 PBS 2.2 RA MG-63 IgG/Bio min PBS HE MG-63 SABC min DAB 5-20 min 1-2 min Olympus BH-2 3-5

3 Progress in Modern Biomedicine 2009 Vol.9 No RA p p27 HE μmol/l RA MG-63 % MG-63 Fig. 2 The influence of RA on the cell cycle of MG-63 cells G 0 /G % DNA S G 2 /M 3 4 MG-63 RA MG-63 (HEⅹ400) Fig. 3, 4 MG-63 cells before and after RA treatment (HEⅹ400) 2.3 MG-63 c-myc c-fos RA MG-63 c-fos c-myc c-myc MG-63 c-myc c-fos 5 RA c-myc Rb p27 RA MG-63 c-myc c-fos Rb p27 6 HMBA MG-63 [2] c-fos MG-63 p21cip1/waf1 7 RA [12] α-synuclein MG-63 c-fos p21 Rb 8 [13] U-937 c-myc 2.4 MG-63 Rb p27 p27 [4,5] S MG % RA MG-63 G 0 /G % S G2/M S 14.4 % G 2 /M 23.8 % HMBA [2] MG-63 A TEI-6363 t, t [6-9] FTC-133 SAC B2 Eca109 U-937 [10-11] G0/G1 1 μmol/lra MG-63 G 0 /G 1 cyclin E p21waf1/cip1 p27kip1 [11] c-myc c-fos RA MG-63 [14] mrna Rb p27 Rb [15] p21 p27 1μmol/LRA MG-63 9 RA MG-63 c-myc c-fos Rb p27

4 8 Progress in Modern Biomedicine 2009 Vol.9 No.1 [6] Kim HJ, Zhao H, Kitaura H, et al. Glucocorticoids suppress bone formation via the osteoclast[j]. J Clin Invest, 2006,116(8): G 1 S [16] [7] Kudawara I, Ueda T, Yoshikawa H,et al. In vivo inhibition of tumour c-myc C-Jun /JNK growth by dexamethasone in murine osteosarcomas [J]. Eur J Cancer, p21cip1/waf1 c-fos Fas [16] 2001,37(13): c-myc [8] Miura D, Uno H, Azuma Y, et al. Effect of the novel prostaglandin A [17] (1) derivative TEI-6363 on ROS17/2.8 cell differentiation in vitro[j]. c-fos Jpn J Phamacol, 2000, 83 (3): [18] p21 p27 Rb [9] Kim YS, Cerbo RM, Hah CK, et al. Growth inhibition of osteosarcoma p27 G1 cell MG-63 by a mixture of trans,trans conjugated linoleic acid isomers: possible mechanistic actions[j]. J Food Sci, 2008, 73(1):T7-15 [19] P27 Zhang [20] Cx43 [10] Jin Ge, Zhao Ji-min, Yang Hong-yan, et al. All-trans retinoic acid and p27 U2OS dimethyl sulfoxide induced expression of wtp53 gene in human G 0 /G 1 Rb esophageal cancer cells[j]. Tumor, 2006,26 (1):14-16 G 1 /S Rb [11] Dimberg A, Bahram F, Karlberg I, et al. Retinoic acid-induced cell [21] Rb cycle arrest of human myeloid cell lines is associated with sequential Rb p53 down-regulation of c-myc and cyclin E and posttranscriptional Rb up-regulation of p27kip1[j]. Blood, 2002, 99(6): [22,23] [12] XIE Yuxin, LIU Yan, ZHANG Jin-gui, et al. Apoptosis induced by resveratrol in human osteosarcoma MG63 cells [J].Hebei Medical Rb p53 Journail, 2007, 29(4): Rb p53 c-myc [13] Fujita M, Sugama S, Nakai M,et al. alpha-synuclein stimulates differentiation of osteosarcoma cells: relevance to down-regulation of [24] MG-63 proteasome activity[j]. J Biol Chem, 2007, 282(8): c-myc c-fos Rb p27 [14] Bringold F, Serrano M. Tumor suppressors and oncogenes in cellular RA c-myc c-fos c-myc senescence[j]. Exp Gerontol, 2000, 35(3): Rb p27 [15] Lai L, Bohnsack BL, Niederreither K, et al. Retinoic acid regulates P27 Rb G 0 /G 1 G 1 /S endothelial cell proliferation during vasculogenesis[j]. Development, G 0 /G 1 S 2003, 130(26): [16] Zhang Zi-zheng, Liu Han-yun, Liang Jin-song. The research of inhibition of proliferation and induction of apoptosis of AHPN in human RA c-myc c-fos Rb p27 non-small cell lung carcinoma cell line H460 in vitro [J]. Journal of Basic Clinical Oncology, 2007, 20(6): MG-63 G0/G1 S [17] Liu Jing-yang, Li Kang-hua, Li Yue-nan. Significance of c-myc protein expression in osteosarcoma [J]. China Journal of Modern MG-63 MG-63 Medicine, 2004, 14(23):66-67 RA MG-63 [18] Sunters A, McCluskey J, Grigoriadis AE. Control of cell cycle gene expression in bone development and during c-fos-induced osteosarcoma References [1] Bachle M, Kohal RJ. A systematic review of the influence of different titanium surfaces on proliferation, differentiation and protein synthesis of osteoblast-like MG63 cells[j]. Clin Oral Implants Res, 2004,15 (6): [2] Ma Zong-yuan, Li Qi-fu, Tang Jian. The Effects of HMBA on Proliferation and Associated Genes Expression of Human Osteosarcoma formation[j]. Dev Genet, 1998, 22(4): [19] Zhang Jing-song, Yang Shu-hua, Chen Shu-wei, et al. Expression of Skp2 and p27 in Osteosarcoma and Their Clinical Significance [J]. Cancer Research on Prevention and Treatment, 2007, 34 (3): , 232 [20] Zhang YW, Morita I, Ikeda M, et al. Connexin43 suppresses proliferation of osteosarcoma U2OS cells through post-transcriptional regulation MG-63 Cells [J]. Journal of Xiamen University (Natural Science), of p27[j]. Oncogene,2001, 20(31): ,46(5): [21] Maitra A, Roberts H, Weinberg AG, et al. Loss of p16 (INK4a) expression [3] Zheng Yan-bin, Wang Guo-hong, Wang Chen, et al. Inhibitory Effects of Tanshinone A on Human Osteosarcoma MG-63 Cell Proliferation[J]. Journal of Xiamen University (Natural Science), 2006, 45(S): 1-5 [4] Friedberg EC. Reversible Monoubiquitination of PCNA:A Novel Slant correlateswith decreased survival in pediatric osteosarcomas[j]. Int J Cancer, 2001, 95(1):34-38 [22] Thomas DM, Carty SA, Piscopo DM, Lee JS, et al. The retinoblastoma protein acts as a transcriptional coactivator required for osteogenic differentiation[j]. Mol Cell, 2001, 8(2): on Regulating Translesion DNA Synthesis [J]. Molecular Cell, [23] Ookawa K, Tsuchida S, Adachi J, et al. Differentiation induced by Rb 2006,22(2): expression and apoptosis induced by p53 expression in an osteosarcoma [5] Dávid Szüts, Christo Christov, Lisa Kitching, et al. Distinct populations of human PCNA are required for initiation of chromosomal DNA replication and concurrent DNA repair [J]. Experimental Cell Research, 2005, 311(2): cell line[j]. Oncogene, 1997, 14(12): [24] Wu CH, van Riggelen J, Yetil A, et al. Cellular senescence is an important mechanismof tumor regression upon c-myc inactivation [J]. Proc Natl Acad Sci, 2007, 104(32):

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