Moriai R, Asanuma K, Kobayashi D, Yajima T, Yagihashi A, Yamada M, Watanabe N
Division of Laboratory Diagnosis, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo 060-8543, Japan.
Anticancer Res. 2001 Jan-Feb;21(1B):595-600.
In this study we investigated expression profiles of the anti-apoptotic gene survivin in malignant human haematopoietic cells.
Using a quantitative TaqMan reverse transcription-polymerase chain reaction, survivin and bcl-2 mRNA expression were examined in 12 malignant haematopoietic cell lines, in 21 patients with haematopoietic malignancies and in normal leukocyte fractions.
Survivin mRNA levels, demonstrable in all 12 malignant cell lines, differed but showed no relationship to the cell of origin. Conversely, no survivin mRNA expression was detected in normal leukocyte fractions. Further, survivin mRNA was expressed in 16 out of 21 patients with malignancies. Five days after treatment of HL-60 cells with a combination of all-trans retinoic acid and tumor necrosis factor, survivin expression decreased to 14.1% of that in untreated cells. Further, survivin mRNA expression in K-562/ADR cells with acquired resistance to adriamycin was 1.7 times that in parent K-562 cells.
Our results indicated the possibility that quantitation of survivin mRNA expression is a useful tool for the detection of haematopoietic tumor cells in clinical laboratory test and that survivin could be a target for treatment of haematopoietic malignancies.
在本研究中,我们调查了抗凋亡基因survivin在人类恶性造血细胞中的表达谱。
使用定量TaqMan逆转录聚合酶链反应,检测了12种恶性造血细胞系、21例造血系统恶性肿瘤患者以及正常白细胞组分中survivin和bcl-2 mRNA的表达。
在所有12种恶性细胞系中均检测到survivin mRNA水平,其存在差异但与细胞来源无关。相反,在正常白细胞组分中未检测到survivin mRNA表达。此外,21例恶性肿瘤患者中有16例表达survivin mRNA。用全反式维甲酸和肿瘤坏死因子联合处理HL-60细胞5天后,survivin表达降至未处理细胞的14.1%。此外,对阿霉素获得耐药性的K-562/ADR细胞中survivin mRNA表达是亲本K-562细胞的1.7倍。
我们的结果表明,在临床实验室检测中,定量检测survivin mRNA表达可能是检测造血肿瘤细胞的有用工具,并且survivin可能成为治疗造血系统恶性肿瘤的靶点。