期刊文献+

细胞运动抑制剂4-甲基-3-硝基-苯甲酸的基础研究 被引量:1

Basic Research of Cell Migration Inhibitor 4-methyl-3-nitro-benzoic Acid
下载PDF
导出
摘要 目的:检测小分子化合物4-甲基-3-硝基-苯甲酸的药物毒性作用、对多种恶性肿瘤细胞运动能力的影响以及在小鼠体内对肿瘤生长的抑制作用。方法:将4-甲基-3-硝基-苯甲酸给药剂量按等比数列排列,从而测定它在小鼠体内的半数致死量;体外采用趋化实验检测4-甲基-3-硝基-苯甲酸对肺癌细胞A549、肝癌细胞SSMC-7721、恶性黑色素瘤细胞LiBr及胃癌细胞MGC-803趋化运动能力的影响;体内实验,将BL6-B16细胞接种到C57小鼠,经灌胃给药后,观察4-甲基-3-硝基-苯甲酸对小鼠移植瘤生长的影响,并以生理盐水作对照,同时以体重变化为指标衡量4-甲基-3-硝基-苯甲酸的毒性作用。结果:4-甲基-3-硝基-苯甲酸在小鼠体内的半数致死量LD50为771.73mg/kg;趋化实验表明4-甲基-3-硝基-苯甲酸对多种肿瘤细胞的细胞运动都有明显的抑制作用,并且最适浓度为2.0μM;4-甲基-3-硝基-苯甲酸抑制小鼠黑色素移植瘤生长,肿瘤体积(P<0.05)和重量(P<0.01)显著低于对照组,4-甲基-3-硝基-苯甲酸对小鼠体重变化无影响。结论:4-甲基-3-硝基苯甲酸有望成为治疗恶性肿瘤的新药。 Objective: To investigate the effects of the micro-molecular compound 4-methyl-3-nitro-benzoic acid on drug toxicity, migration capacity of various malignant tumor cells and inhibition of tumor growth on mice. Methods: The dosage of 4-methyl-3-nitro-benzoic acid was arranged by geometric series, and then the half lethal dose was measured on mice in vivo. Chemotaxis assay was performed to detect the effects of 4-methyl-3-nitro-benzoic acid on cell migration capacity of the lung cancer cells A549, liver cancer cells SSMC-7721, malignant melanoma cells LiBr and gastric cancer cells MGC-803 in vitro. In vivo, BL6-B16 cells were injected to C57 mice with normal sodium as the control. The effects of 4-methyl-3-nitro-benzoic acid on the growth of the mouse-transplanted tumors were observed after intra-gastric administration. The body weight of the mice was recorded as another measure to estimate the toxic effect of the drug, 4-methyl-3-nitro-benzoic acid. Results: It was shown by acute toxicity testing that the half lethal dose (LD50) of 4-methyl-3-nitro-benzoic acid in mice in vivo is 771.73 mg/kg. Chemotaxis assay showed that 4-methyl-3-nitro-benzoic acid could overtly and markedly inhibit the cell migration of many tumor cells with 2.0 μM as the optimal inhibiting concentration. 4-methyl-3-nitro-benzoic acid could inhibit the growth of mouse-transplanted melanoma, and the tumor volume (P〈0.05) and tumor weight (P〈 0.01) was markedly lower compared to the control group. 4-methyl-3-nitro-benzoic acid demonstrated no effect on body weight change in mice. Conclusions: 4-methyl-3-nitro-benzoic acid promises to be an effective new drug used in the treatment of malignant tumors.
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2010年第11期601-604,共4页 Chinese Journal of Clinical Oncology
基金 国家自然科学基金资助(编号:30772529)~~
关键词 恶性肿瘤 细胞运动 肿瘤抑制 肿瘤治疗 Malignant neoplasm Cell migration Tumor suppression Cancer therapy
  • 相关文献

参考文献14

  • 1Parkin DM,Bray F,Ferlay J,et al.Global cancer statistics,2002[J].CA Cancer J Clin,2005,55(2):74-108. 被引量:1
  • 2马雯,谢德荣,曹婉萍,杨琼,江志敏,陈邓林,毕卓菲,张媛冬.乙型肝炎病毒感染与胰腺癌相关性研究[J].中国肿瘤临床,2009,36(24):1388-1390. 被引量:5
  • 3Wan W,Zou H,Sun R,et al.Investigate the role of PTEN in chemotaxis of human breast cancer cells[J].Cell Signal,2007,19(11):2227-2236. 被引量:1
  • 4Yang XJ.Multisite protein modification and intramolecular signaling[J].Oncogene,2005,24(10):1653-1662. 被引量:1
  • 5Brough PA,Aherne W,Barril X,et al.4,5-diarylisoxazole Hsp90 chaperone inhibitors:potential therapeutic agents for the treatment of cancer[J].J Med Chem,2008,51(2):196-218. 被引量:1
  • 6Giamas G,Stebbing J,Vorgias CE,et al.Protein kinases as targets for cancer treatment[J].Pharmacogenomics,2007,8(8):1005-1016. 被引量:1
  • 7Saxena A.Cancer chemotherapy and its side effect management[J].Nurs J India,2006,97(5):109-110. 被引量:1
  • 8Abali H,Celik I.Tropisetron,ondansetron,and granisetron for control of chemotherapy-induced emesis in Turkish cancer patients:a comparison of efficacy,side-effect profile,and cost[J].Cancer Invest,2007,25(3):135-139. 被引量:1
  • 9Itoi A,Takashima M,Ishimasa H,et al.Adjuvant chemotherapy with TS-1 for head and neck cancer-side effect of two-week application followed by one-week rest regimen[J].Gan To Kagaku Ryoho,2006,33(5):617-620. 被引量:1
  • 10Ben-Baruch A.Organ selectivity in metastasis:regulation by chcmokines and their receptors[J].Clin Exp Metastasis,2008,25(4):345-356. 被引量:1

二级参考文献15

  • 1Yoshiki Katakura,Hiroshi Yotsuyanagi,Kiyoe Hashizume,Chiaki Okuse,Noriaki Okuse,Kohji Nishikawa,Michihiro Suzuki,Shiro Iino,Fumio Itoh.Pancreatic involvement in chronic viral hepatitis[J].World Journal of Gastroenterology,2005,11(23):3508-3513. 被引量:5
  • 2Wan DF,Gong Y,Qin WX,et al.Large-scale cDNA transfection screening for genes related to cancer development and progression[J].Proc Natl Acad Sci,2004,101(44):15724~15729 被引量:1
  • 3Corbett SA,Schwarzbauer JE.Fibronectin-fibrin cross-linking:a regulator of cell behavior[J].Trends Cardiovasc Med,1998,8(8):357~362 被引量:1
  • 4Matsui S,Takahashi T,Oyanagi Y,et al.Expression,localization and alternative splicing pattern of fibronectin messenger RNA in fibrotic human liver and hepatocellular carcinoma[J].J Hepatol,1997,27(5):843~853 被引量:1
  • 5Yang Y,Dang D,Atakilit A,et al.Specific alpha v integrin receptors modulate K1735 murine melanoma cell behavior[J].Biochem Biophys Res Commun,2003,308(4):814~819 被引量:1
  • 6Li Y,Yang J,Dai C,et al.Role for integrin-linked kinase in mediating tubular epithelial to mesenchymal transition and renal interstitial fibrogenesis[J].J Clin Invest,2003,112(4):503~516 被引量:1
  • 7Ray JM,Stetler-Stevenson WG.Gelatinase A activity directly modulates melanoma cell adhesion and spreading[J].EMBO J,1995,14(5):908~917 被引量:1
  • 8Pereda MP,Hopfner U,Pagotto U,et al.Retinoic acid stimulates meningioma cell adhesion to the extracellular matrix and inhibits invasion[J].BrJ Cancer,1999,81(3):381~386 被引量:1
  • 9Ueda M,Terai Y,Kumagai K,et al.Correlation between thymidine phosphorylase expression and invasion phenotype in cervical carcinoma cells[J].IntJ Cancer,2001,91(6):778~782 被引量:1
  • 10刘奇才,郜峰,程祖建,廖冬妹,欧启水.戊型肝炎病毒感染与胰腺癌发生的关系[J].检验医学与临床,2007,4(11):1031-1032. 被引量:2

共引文献7

同被引文献1

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部