Ramachandran C, Melnick S J, Escalon E, Jhabvala P, Khatib Z, Alamo A, Smith S
Division of Pathology, Research Institute, Miami Children's Hospital, Miami, FL 33155, USA. cheppail.ramachandran@
Anticancer Res. 2000 Sep-Oct;20(5C):3759-65.
The expression of genes associated with apoptosis, cell proliferation and drug resistance in tumor cells was investigated in two pediatric Wilms' tumor patients (MCH-WT-1 and MCH-WT-3) for their association with cell cycle, daunorubicin accumulation and clinical data. DNA content, cell cycle and drug accumulation were analyzed immediately after surgery by flow cytometry and mRNA expression by reverse transcriptase-polymerase chain reaction (RT-PCR) assay. Primary cell cultures were established from tumor specimens and tumor cells in both cases showed epithelial morphology. Although cell proliferation markers (Ki67 and PCNA) were expressed in both cases, MCH-WT-3 showed higher levels of mRNA expression, which corresponded, with metastatic behavior of the tumor in the patient. While p53 and p21 mRNAs were expressed at low levels in MCH-WT1, MCH-WT-3 showed high levels of p21 mRNA only. The increased expression of cyclin kinase inhibitor (p21) in MCH-WT-3 compared to MCH-WT-1 correlated with a higher percentage of G0/G1 cell population in the tumor specimen. Despite the expression of multidrug resistance markers (MDR1 and LRP) in MCH-WT-1, flow cytometric analysis showed tumor cell populations with very low and high daunorubicin accumulation and with the absence of any effect for verapamil and dipyridamole on daunorubicin accumulation of tumor cells.
在两名小儿肾母细胞瘤患者(MCH-WT-1和MCH-WT-3)中,研究了肿瘤细胞中与细胞凋亡、细胞增殖和耐药性相关基因的表达情况,以及它们与细胞周期、柔红霉素蓄积和临床数据的关联。术后立即通过流式细胞术分析DNA含量、细胞周期和药物蓄积情况,并通过逆转录聚合酶链反应(RT-PCR)检测mRNA表达。从肿瘤标本中建立原代细胞培养,两例患者的肿瘤细胞均显示出上皮形态。虽然两例患者均表达细胞增殖标志物(Ki67和PCNA),但MCH-WT-3的mRNA表达水平较高,这与该患者肿瘤的转移行为相符。MCH-WT1中p53和p21 mRNA表达水平较低,而MCH-WT-3仅显示p21 mRNA高水平表达。与MCH-WT-1相比,MCH-WT-3中细胞周期蛋白激酶抑制剂(p21)表达增加,这与肿瘤标本中较高比例的G0/G1细胞群体相关。尽管MCH-WT-1中表达多药耐药标志物(MDR1和LRP),但流式细胞术分析显示肿瘤细胞群体中柔红霉素蓄积量极低和极高,且维拉帕米和双嘧达莫对肿瘤细胞柔红霉素蓄积无任何影响。