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小分子化合物G-749抑制胃癌细胞增殖和迁移

Small molecule compound G-749 suppresses the proliferation and migration of gastric cancer cells
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摘要 目的 研究小分子化合物G-749对人胃癌细胞MGC803和SGC7901的增殖和迁移的影响。方法 分别用不同浓度的G-749处理MGC803和SGC7901两种人胃癌细胞,CCK8实验和克隆形成实验检测G-749对胃癌细胞增殖的影响,流式细胞术检测化合物对细胞周期的影响,划痕实验检测G-749对胃癌细胞迁移的影响。结果 化合物G-749能够抑制人胃癌细胞MGC803和SGC7901的增殖并存在剂量依赖关系,抑制细胞G_(0)/G_(1)期向S期的转变,并能明显抑制胃癌细胞的迁移。结论 化合物G-749对胃癌细胞有抑制作用,有望应用于胃癌细胞的治疗。 Objective eTo investigate the effects of small molecule compound G-749 on the proliferation and migration of human gastric cancer cells MGC803 and SGC7901.Methods MGC803 and SGC7901 human gastric cancer cells were treated with different concentrations of G-749.CCK8 assay and colony formation assay were used to detect the effect of G-749 on the proliferation of gastric cancer cells.Flow cytometry was used to check the effect of G-749 on the cell cycle.The scratch test was used to identity the effect of G-749 on the migration of gastric cancer cells.Results The compound G-749 inhibited the proliferation of human gastric cancer cells MGC803 and SGC7901 in a dose-dependent manner,and inhibited the transition of cells from G_(0)/G_(1) phase to S phase,and suppressed the migration of gastric cancer cells.Conclusion Compound G-749 has inhibitory effect on gastric cancer cells and is expected to be used in the treatment of gastric cancer cells.
作者 蔺炜然 张健 李丰 LIN Wei-ran;ZHANG Jian;LI Feng(Department of Laboratory Medicine,General Hospital of Northern Theater Command,Shenyang 110016;Department of Molecular Cell Biology,Key Laboratory of Medical Cell Biology of Public Health Ministry of China,School of Life Sciences,China Medical University,Shenyang 110122,China)
出处 《解剖科学进展》 CAS 2024年第1期47-50,共4页 Progress of Anatomical Sciences
基金 国家自然科学基金(31771553)。
关键词 胃癌 G-749 增殖 细胞周期 gastric cancer G-749 proliferation cell cycle
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  • 1Santiago González-Moreno,Luis A González-Bayón,Gloria Ortega-Pérez.Hyperthermic intraperitoneal chemotherapy:Rationale and technique[J].World Journal of Gastrointestinal Oncology,2010,2(2):68-75. 被引量:17
  • 2Tang L, Zhao S, Liu W, et al. Diagnostic accuracy of circulating tumor ceils detection in gastric cancer: systematic review and meta- analysis[J]. BMC Cancer, 2013, 13: 314.
  • 3Kulig J, Koodziejczyk P, Kulig P, et al. Targeted therapy for gastric cancer--current status[J]. J Oncol Pharm Pract, 2013, 19(1): 75-81.
  • 4Kim JG. Molecular targeted therapy for advanced gastric cancer[J]. Korean J Intern Med, 2013, 28(2): 149-155.
  • 5Smyth EC, Cunningham D. Targeted therapy for gastric cancer[J]. Curr Treat Options Oneol, 2012, 13(3): 377-389.
  • 6Liang S, Mu K, Wang Y, et al. CyclinD1, a prominent prognostic marker for endometrial diseases[J]. Diagn Pathol, 2013, 8: 138.
  • 7Wang MT, Chen G, An SJ, et al. Prognostic significance of cyclinD1 amplification and the co-alteration of cyclinD1/pRb/ppRb in patients with esophageal squamous cell carcinoma[J]. Dis Esophagus, 2012, 25(7): 664-670.
  • 8Huang CZ, Huang WZ, Zhang G, et al. In vivo study on the effects of curcumin on the expression profiles of anti-tumour genes (VEGF,CyclinD1 and CDK4) in liver of rats injected with DEN[J]. Mol Biol Rep, 2013, 40(10): 5825-5831.
  • 9Feng Z, Chen J, Wei H, et al. The risk factor of gallbladder cancer: hyperplasia of mucous epithelium caused by gallstones associates with pl6/CyclinD1/CDK4 pathway[J]. Exp Mol Pathol, 2011, 91(2): 569-577.
  • 10朱忠政,王爱忠,贾杭若,金夏祥,何向蕾,朱冠山.细胞周期蛋白D1基因多态与人结直肠癌遗传易感性[J].解剖科学进展,2008,14(4):357-360. 被引量:4

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