付文娟, 李琪佳, 甘洪全, 孙芳初, 王连立. TRAIL、 Ki-67蛋白在人骨肉瘤中表达及其与肿瘤细胞增殖和凋亡的关系[J]. 中国肿瘤临床, 2011, 38(1): 20-23 . DOI: 10.3969/j.issn.1000-8179.2011.01.005
引用本文: 付文娟, 李琪佳, 甘洪全, 孙芳初, 王连立. TRAIL、 Ki-67蛋白在人骨肉瘤中表达及其与肿瘤细胞增殖和凋亡的关系[J]. 中国肿瘤临床, 2011, 38(1): 20-23 . DOI: 10.3969/j.issn.1000-8179.2011.01.005

TRAIL、 Ki-67蛋白在人骨肉瘤中表达及其与肿瘤细胞增殖和凋亡的关系

  • 摘要: 目的:通过观察TRAIL、Ki-67在人骨肉瘤组织中的表达规律及其相互关系,探讨二者与骨肉瘤细胞增殖、 凋亡的相关性。方法: 用免疫组织化学方化法检测TRAIL、 Ki-67蛋白在骨肉瘤及骨软骨瘤中的表达, 用TUNEL方法通过激光扫描共聚焦显微镜检测骨肉瘤及骨软骨瘤组织中的细胞凋亡分布情况并计算增殖和凋亡指数。结果:骨肉瘤组织TRAIL蛋白表达强度低于骨软骨瘤 (t=-5.51, P<0.05); 而Ki-67蛋白表达高于骨软骨瘤 (t=17.69, P<0.05)。TRAIL和Ki-67在骨肉瘤中的表达呈负相关 (r=-0.844 4,P<0.01)。骨肉瘤中细胞凋亡指数 (AI) 显著低于骨软骨瘤 (P<0.01); 而增殖指数 (PI) 显著高于骨软骨瘤 (P<0.01)。骨肉瘤中Ki-67蛋白表达与细胞凋亡指数之间呈负相关 (r=-0.562 2, P<0.01); 而TRAIL蛋白表达与细胞凋亡指数呈正相关 (r=0.635 0, P<0.01), 而与增殖指数呈负相关 (r=-0.553 0, P<0.01)。结论: TRAIL参与细胞凋亡的调控, 可能是诱导骨肉瘤细胞凋亡的分子基础之一; Ki-67在肿瘤细胞的增殖与凋亡中具有重要作用, 骨肉瘤组织中Ki-67明显过表达, 而TRAIL蛋白表达明显下调, 表明两者在骨肉瘤的发生、 发展中起拮抗作用。如能抑制Ki-67的表达,促进TRAIL的表达, 有可能提高骨肉瘤细胞的凋亡敏感性。

     

    Abstract: Expression of TRAIL and Ki-67 in Human Osteosarcoma and Its Correlation with Apoptosisand Proliferation of Tumor CellsWenjuan FU1, Qijia LI2, Hongquan GAN2, Fangchu SUN1, Lianli WANG1Correspondence to: Qijia LI, E-mail: qjl1222@hotmail.com1Department of Radio-chemotherapy, Tangshan People's Hospital, Tangshan 063000, China2Experimental Center, North China Coal Medical College,Tangshan 063000, ChinaThis work was supported by Hebei Provincial Bureau of Personnel Funds for Scientific Activities of Returned Overseas Stu-dent (No. 2009-11)Abstract Objective: To investigate the expression and distribution of TRAIL and Ki-67 proteins, as well as the relation-ship between these proteins and the proliferation and apoptosis of human osteosarcoma cells. Methods: Immunohistochem-istry was used to evaluate the distribution of TRAIL and Ki-67 proteins in groups of patients with either osteosarcoma or os-teochondroma. Apoptosis was detected by In Situ Terminal Deoxy-nucleotide Transferase Labeling (TUNEL), and apoptoticcells could be seen when FITC labeling was examined with confocal laser scanning microscopy. The proliferation indexand apoptosis index were then calculated. Results: The positive expression of TRAIL protein in osteosarcoma was signifi-cantly lower than that in osteochondroma ( t = -5.51, P < 0.05), while the positive expression of Ki-67 protein was signifi-cantly higher in the osteosarcoma group than in the osteochondroma group ( t = 17.69, P < 0.05). There was a significantnegative correlation between TRAIL and Ki-67 protein expression in osteosarcoma ( r = -0.8444, P < 0.01). The apoptosisindex (AI) was lower in the osteosarcoma group than in the osteochondroma group ( P < 0.01). The proliferation index (PI)was higher in the osteosarcoma group than in the osteochondroma group ( P < 0.01). There was a negative correlation be-tween Ki-67 protein expression and the AI ( r = -0.5622, P < 0.01). There was a positive correlation between TRAIL proteinexpression and the AI ( r = 0.6350, P < 0.01) and a negative correlation between TRAIL protein expression and the PI (r = -0.5530, P < 0.01). Conclusion: TRAIL protein is important in inducing apoptosis of osteosarcoma cells and it takes partin the process of cellular apoptosis. Ki-67 protein plays an important role in the proliferation and apoptosis of osteosarco-ma. The significant overexpression of Ki-67 and underexpression of TRAIL protein in osteosarcoma may be closely relatedto the occurrence and development of osteosarcoma. Lowering Ki-67 overexpression and raising TRAIL underexpressionmay increase apoptosis in osteosarcoma cells.Key words Osteosarcoma; TRAIL; Ki-67; Apoptosis

     

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