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全反式维甲酸对涎腺腺样囊性癌细胞株Acc-M体外抗增殖作用的研究 被引量:3

EFFICACY OF ALL TRANS RETINOIC ACID IN INHIBITION OF HUMAN SALIVARY ADENOID CYSTIC CARCINOMA CELL PROLIFERATION IN VITRO
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摘要 目的维甲酸类化合物能预防头颈部癌前病变转变为癌,并能有效地降低头颈部第二原发癌的发生率。近来研究证实,维甲酸对头颈部鳞癌有诱导分化治疗作用,但维甲酸对头颈部腺癌诱导分化作用研究少见报道。方法本研究采用克隆形成法、MTT检测法以及细胞周期测定技术,把全反式维甲酸(altransretinoicacidA-TRA)对人涎腺腺样囊性癌细胞株(AccM)的体外抗增殖作用和细胞增殖周期进行了观察。结果显示,ATRA对AccM细胞有一定抗增殖作用,且该作用与浓度、时间呈依赖关系;AccM细胞经ATRA作用72小时后其S期比例明显下降,同时G0+G1期比例上升。结论研究表明,5~20μmol/L浓度的ATRA对AccM细胞产生抗增殖作用。 Retinoids are proved to prevent carcinogenesis in head and neck premalignant lesions and to prevent second primary carcinoma in patients with head and neck cancer. Recent studies have demonstrated the efficacy of retinoic acid in inducing differentiation therapy of carcinoma. In the present study, all trans retinoic acid was tested for its antiproliferative activity aganist human salivary adenoid cystic carcinoma cell(AccM) in vitro. Clonogenic assay and MTT assay as well as cell cycle analysis were used in this experiment. These observations showed that ATRA can inhibit the growth of AccM cell with does and time response manner. The decrease in proportions of cells in Sphase was detected following 72 h of treatment, this was accompanied by an increase of cell in G0 and G1. These results indicated that proliferation of AccM can be inhibited by higher concentrations of ATRE.
出处 《口腔颌面外科杂志》 CAS 1998年第1期12-14,共3页 Journal of Oral and Maxillofacial Surgery
基金 国家自然科学基金
关键词 涎腺 腺样囊性癌 全反式维甲酸 治疗 抗增殖 AccM cell line All trans retinoic acid Antiproliferation Induced differentiation therapy
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  • 1黎伯铨,张雪艳,蔡岩,王秀琴,魏文,毛宝龄,吴旻.维甲酸对人肺腺癌细胞系分化作用的实验研究[J].中华医学杂志,1995,75(11):683-685. 被引量:12
  • 2关晓峰,邱蔚六,何荣根,林国础,周晓健.肺高转移性涎腺腺样囊性癌细胞株的筛选[J].中华口腔医学杂志,1996,31(2):74-77. 被引量:39
  • 3卢友光,周鸿鹰,丁林灿,梅妍,熊若虹,邓世山,羊惠君.涎腺腺样囊性癌高、低转移细胞系基因表达谱及基质金属蛋白酶表达差异[J].中华医学遗传学杂志,2006,23(5):505-510. 被引量:18
  • 4陈智 樊明文 等.原位TUNEL法检测细胞凋亡[J].口腔医学纵横,1998,14(4):251-253.
  • 5Kamb A, Gruis NA,Weaver-Feldhaus J,et al.A cell cycle regulator potentially involved in genesis of many tumor types.Science,1994,264∶436-439
  • 6Krvemer G,Iamzmi N,Susin S.Mitochondrial Control of apoptosis.Immunol Today,1997∶18-44
  • 7Hornebeck W,Lambert E,Petitfrere E,et al.Beneficial and detrimental influences of tissue inhibitor of metalloproteinase-1(TIMP-1) in tumor progression[J].Biochimie,2005,87(3-4):377-383.
  • 8Yamashita K,Azumano I,Mai M,et al.Expression and tissue localization of matrix metalloproteinase 7 (matrilysin) in human gastric carcinomas.Implications for vessel invasion and metastasis[J].Int J Cancer,1998,79(2):187-194.
  • 9Adachi Y,Yamamoto H,Itoh F,et al.Contribution of matrilysin(MMP-7) to the metastatic pathway of human colorectal cancers[J].Gut,1999,45(2):252-258.
  • 10Yoshizaki T,Maruyama Y,Sato H,et al.Expression of tissue inhibitor of matrix metalloproteinase-2 correlates with activation of matrix metalloproteinase-2 and predicts poor prognosis in tougue squamous cell carcinoma[J].Int J Cancer,2001,95(1):44-50.

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