期刊文献+

苯乙酸钠增强肿瘤细胞表面HLA分子的表达 被引量:5

Sodium Phenylacetate Enhances HLA Molecule Expression on the Surface of Tumor Cells
下载PDF
导出
摘要 以分化绣导剂苯乙酸钠处理肿瘤细胞,以ELISA检测肿瘤细胞表面HLA Ⅰ、Ⅱ类分子表达的变化。结果发现MCF-7、MDA-453、MKN-45以及Hela细胞表面HLA Ⅰ类分子表达较低,而MKN-28和3AO细胞表面HLA Ⅰ类分子高表达。MDA-453、MKN-28、MKN-45、Hela以及3AO细胞表面亦表达HLA Ⅱ类分子,而MCF-7细胞表面缺乏HLA Ⅱ类分子。苯乙酸钠能够诱导MCF-7细胞表面表达HLA Ⅱ类分子;增强MCF-7细胞表面HLA Ⅰ类分子,MDA-453、MKN-28、MKN-45、Hela以及3AO细胞表面HLA Ⅰ、Ⅱ类分子的表达。并且肿瘤细胞表面HLA Ⅰ类分子的表达与苯乙酸钠的作用时间和剂量呈正相关。 Sodium phenylacetate can induce differentiation of tumor cells and has been approved as a drug for the treatment of adults with cancer. In order to explore the immunological mechanism of its antitumor effect, the influence of sodium phenylacetate on HLA class I and II molecule expression in various human tumor cell lines, including breast adenocarcinoma (MCF-7.MUA-453), gastrocarcinoma(MKN-28,MKN-45), ovarian cancer(3AO) and cervical cancer(Hela), was studied with ELISA. The result showed that HLA class II molecule was absent from the surface of MCF-7 cells, but they could be induced after 7 days of continued treatment with sodium phenylacetate. Sodium phenylacetate was found to increase HLA class I molecule expression on the surface of MCF-7 cells, HLA class 1 and II molecule expression on the surface of MDA-453、 MKN-28、 MKN-45、 Hela and 3AO cells. The effect of sodium phenylacetate on HLA class I molecule expression in tumor cells is dose-and time-dependent.
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 1996年第4期268-271,共4页 Chinese Journal of Cancer Biotherapy
基金 上海市高校博士点建设基金(03509000)
关键词 苯乙酸钠 肿瘤细胞 表面HLA分子 表达 ELISA sodium phenylacetate tumor cells ELISA: HLA molecules
  • 相关文献

同被引文献36

  • 1[1]Coffey RN, Watson RW, Fitzpatrick JM, et al. Androgen-mediated resistance to apoptosis [J]. Prostate, 2002, 53:300 ~ 309.
  • 2[2]Mceleny KR, Watson RW, Coffey RN, et al. Inhibitors of apoptosis proteins in prostate cancer cell lines [J]. Prostate, 2002, 51(2): 133~ 140.
  • 3[4]Samid D, Hudgins W, Shack S, et al. Phenylacetate and pheylbutyrate as novel, nontoxic differentiation inducers [J].Adv Exp Med Biol, 1997,400A:501~ 505.
  • 4[5]Samid D, Shack S, Sherman LT. Phenylacetate:a novel nontoxic inducer of tumor cell differentiation[J].Cancer Research, 1992,52:1988 ~ 1992.
  • 5[6]Nicoletti I, Migliorati G, Pagliacci MC, et al. A rapid and smiple method for measuring thym ocytle apoptosis by propidium iodide staining and flow cytometry[J]. J Immunol Methods, 1991,139:271~279.
  • 6[7]Ross R.Platelet derived growth factor[J].Lancet, 1999,11:1179~ 1182.
  • 7[8]Antoniades HN, Hunkapiller MW. Human platelet derived growth factor (PDGF):amino terminal amino acid sequence [J].Science, 1999,230:963~ 965.
  • 8[9]Jin HM, Robinson DF, Liang Y,et al. SIS/PDGF-B promoter isolation and characterization of regulatory elements necessary for basal expression of the SIS/PDGF-B gene in U2-osteosarcoma cells[J].J Biol Chem,1994, 269:28648 ~28654.
  • 9[10]Wang ZY, Madden SL, Deuel TF, et al. The Wilms tumor gene product, WT1, represses transcription of the plateletderived growth factor A chain gene[J].J Biol Chem, 1999,267:21999 ~ 22002.
  • 10[11]Uehara H, kim SJ, Karashima T, et al. Effects of blocking platelet-derived growth factor-receptor signaling in a mouse model of experimental prostate cancer bone metastases [J].J Natl Cancer Inst, 2003,95(6):458~470.

引证文献5

二级引证文献4

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