南方医科大学学报 ›› 2004, Vol. 24 ›› Issue (07): 779-783.

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葡萄糖神经酰胺合酶基因在多药耐药肿瘤细胞株KBV200的表达及其与肿瘤多药耐药性的关系

杨泉, 张健, 汪森明, 张积仁   

  1. 第一军医大学珠江医院肿瘤中心, 广东, 广州, 510282
  • 出版日期:2004-07-20 发布日期:2004-07-20
  • 基金资助:
    收稿日期:2004-2-16。
    基金项目:广东省自然科学基金(001041)
    作者简介:杨泉,男,第一军医大学在读硕士研究生,电话:020-88527960

Expression of glucosylceramide synthase mRNA in vincristine-resistant KBV200 cell line in association with multidrug resistance

YANG Quan, ZHANG Jian, WANG Sen-ming, ZHANG Ji-ren   

  1. 第一军医大学珠江医院肿瘤中心, 广东, 广州, 510282
  • Online:2004-07-20 Published:2004-07-20

摘要: 目的 观察葡萄糖神经酰胺合酶(glucosylcerarnide synthase,GCS)基因在人口腔表皮样癌多药耐药细胞株KBV200的表达及其与肿瘤多药耐药性(MDR)的关系。方法 采用RT-PCR分析KBV200及其亲本KB细胞株GCS基因表达的差异,运用MTT法分析KBV200经糖脂合成酶抑制剂苯基棕榈酰胺吗啡丙醇(DL-PPMP)及钙离子通道阻滞剂异搏定处理前后细胞MDR的变化,应用RT-PCR技术检测KBV200细胞耐药逆转后GCS及mdrl基因的表达。结果 KBV200细胞GCS和mdrl基因的表达明显强于KB细胞,而KB细胞mdrl基因表达为阴性。5~25μmol/L DL-PPMP均可抑制KBV200GCS mRNA表达,25 μmol/L时抑制强度最大;10 μmol/L异搏定即可抑制KBV200GCS mRNA表达,15 μmol/L时抑制作用明显。DL-PPMP和异搏定均可抑制mdrl基因的表达,KBV200经25μmol/L DL-PPMP作用48h后细胞内mdrl表达为阴性。结论 异搏定和DL-PPMP对GCS和marl基因表达的抑制调节呈浓度依赖性,它们可通过抑制GCS和mdrl基因表达,逆转KBV200对长春新碱的耐药。KBV200GCS基因的表达与MDR存在正相关,GCS基因可能在肿瘤的多药耐药过程中起着重要作用。

Abstract: Objective To investigate the relationship between the expression of glucosylceramide synthase (GCS) mRNA in vincristine-resistant KBV200 human cancer cell line and multidrug resistance (MDR) of the cancer cells. Methods Reverse transcriptional polymerase chain reaction (RT-PCR) was employed to analyze the differential expression of GCS mRNA between KBV200 and KB cell lines and the changes in the mRNA expressions of GCS and mdrl gene in KBV200 cells after reversion of MDR. The effects of de-phenyl-z-palmaitoylamino-3-morpholine-1-propanol (DL-PPMP) and verapamil in reversing MDR of the cells were evaluated by MTT assay. Results KBV200 cells exhibited significantly increased expressions of GCS and mdrl gene, whereas mdrl gene failed to be detected in the parental KB cells. DL-PPMP within the concentrations ranging from 5 to 25 μmol/L could inhibit the expression of GCS gene, with the maximum inhibition achieved at 25 μmol/L. Verapamil at the concentration of 10 μmol/L was already sufficient to induce inhibition of GCS expression in KVB200 cells, which was more manifest with the concentration of 15 μmol/L. DL-PPMP and verapamil were found to inhibit mdrl gene expression in KBV200 cells at the mRNA level, and complete inhibition occurred after a 48-hour DL-PPMP treatment at 25 μmol/L. Conclusion The inhibition of GCS and mdrl gene expressions is positively correlated with the concentrations of DL-PPMP and verapamil, which can reverse MDR by inhibiting synthesis of GCS and mdrl gene, indicating the positive correlation between the expression of GCS gene and MDR in KBV200 cells. GCS gene might play an importantrole in MDR during tumor progression.

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