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WT1基因表达对髓系白血病细胞系细胞生长和增殖的影响。

Effect of WT1 gene expression on cell growth and proliferation in myeloid leukemia cell lines.

作者信息

Mi Y, Wang L, Bian S, Meng Q, Chen G, Wang J

机构信息

Institute of Hematology and Blood Diseases Hospital, CAMS, PUMC, Tianjin 300020, China.

出版信息

Chin Med J (Engl). 1999 Aug;112(8):705-8.

Abstract

OBJECTIVE

To investigate the effects and mechanism of Wilms' tumor (WT1) antisense oligonucleotides (AS-oligomers) on proliferation and apoptosis in myeloid leukemia cell lines.

METHODS

K562 and HL-60 cells were cultured in presence of WT1 oligomers. Both cell lines express WT1 gene with no p53 protein expression. Cells growth, apoptosis and expression of WT1, bcl-2 genes were analysed using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenylmetrazolium bromide (MTT) colorimetric assay, flow cytometry and reverse transcription-polymerase chain reaction (RT-PCR) methods.

RESULTS

WT1 antisense oligonucleotides inhibited cellular proliferation of K562 cells and the effect was concentration-dependent. When cultured at concentration of 200 micrograms/ml oligomers, growth inhibition was 46.2% for antisense oligonucleotide cultivated group and 28.1% for sense oligonucleotide cultured group (P = 0.008) respectively. WT1 antisense oligonucleotide can induce apoptosis of K562 and HL-60 cells. Percentages of apoptotic cells in antisense oligonucleotide and sense oligonucleotide treated groups were 30.88% versus 13.62% for K562 cells and 40.15% versus 4.23% for HL-60 cells. However the growth of HL-60 cells and expression of bcl-2 gene were unaffected.

CONCLUSIONS

The WT1 gene is related with proliferation and apoptosis of leukemic cells. Effect of anti-apoptosis may be independent of the cellular p53 status and bcl-2 expression. WT1 gene may play an important role in leukemogenesis.

摘要

目的

研究肾母细胞瘤(WT1)反义寡核苷酸(AS-寡聚物)对髓系白血病细胞系增殖和凋亡的影响及其机制。

方法

将K562和HL-60细胞在WT1寡聚物存在的情况下进行培养。这两种细胞系均表达WT1基因且无p53蛋白表达。采用3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴盐(MTT)比色法、流式细胞术和逆转录-聚合酶链反应(RT-PCR)方法分析细胞生长、凋亡以及WT1、bcl-2基因的表达。

结果

WT1反义寡核苷酸抑制K562细胞的增殖,且该作用呈浓度依赖性。当寡聚物浓度为200微克/毫升时培养,反义寡核苷酸培养组的生长抑制率为46.2%,正义寡核苷酸培养组为28.1%(P = 0.008)。WT1反义寡核苷酸可诱导K562和HL-60细胞凋亡。K562细胞反义寡核苷酸处理组和正义寡核苷酸处理组的凋亡细胞百分比分别为30.88%和13.62%,HL-60细胞分别为40.15%和4.23%。然而HL-60细胞的生长及bcl-2基因的表达未受影响。

结论

WT1基因与白血病细胞的增殖和凋亡相关。抗凋亡作用可能独立于细胞的p53状态和bcl-2表达。WT1基因可能在白血病发生中起重要作用。

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